- Y Diweddaraf sydd Ar Gael (Diwygiedig)
- Pwynt Penodol mewn Amser (01/01/2007)
- Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE)
Directive 1999/45/EC of the European Parliament and of the Council of 31 May 1999 concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (repealed)
When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.
Mae unrhyw newidiadau sydd wedi cael eu gwneud yn barod gan y tîm yn ymddangos yn y cynnwys a chyfeirir atynt gydag anodiadau.Ar ôl y diwrnod ymadael bydd tair fersiwn o’r ddeddfwriaeth yma i’w gwirio at ddibenion gwahanol. Y fersiwn legislation.gov.uk yw’r fersiwn sy’n weithredol yn y Deyrnas Unedig. Y Fersiwn UE sydd ar EUR-lex ar hyn o bryd yw’r fersiwn sy’n weithredol yn yr UE h.y. efallai y bydd arnoch angen y fersiwn hon os byddwch yn gweithredu busnes yn yr UE. EUR-Lex Y fersiwn yn yr archif ar y we yw’r fersiwn swyddogol o’r ddeddfwriaeth fel yr oedd ar y diwrnod ymadael cyn cael ei chyhoeddi ar legislation.gov.uk ac unrhyw newidiadau ac effeithiau a weithredwyd yn y Deyrnas Unedig wedyn. Mae’r archif ar y we hefyd yn cynnwys cyfraith achos a ffurfiau mewn ieithoedd eraill o EUR-Lex. The EU Exit Web Archive legislation_originated_from_EU_p3
Version Superseded: 20/01/2009
EU Directives are published on this site to aid cross referencing from UK legislation. Since IP completion day (31 December 2020 11.00 p.m.) no amendments have been applied to this version.
See 2.2.5 of Annex VI to Directive 67/548/EEC.
Method for the determination of oxidising properties of preparations containing organic peroxides.
See point 2.2.2.1 of Annex VI to Directive 67/548/EEC.
Method for the determination of oxidising properties
See 9.1.1.2 of Annex VI to Directive 67/548/EEC.
Method for the determination of flammability properties
See 9.1.1.1 of Annex VI to Directive 67/548/EEC.
An assessment must be made for all the health effects corresponding to the health effects of substances contained in a preparation. This conventional method described in Parts A and B of this Annex is a calculation method which is applicable to all preparations and which takes into consideration all the health hazards of substances contained in the preparation. For that purpose the dangerous health effects have been subdivided into:
acute lethal effects;
non-lethal irreversible effects after a single exposure;
severe effects after repeated or prolonged exposure;
corrosive effects, irritant effects;
sensitising effects;
carcinogenic effects, mutagenic effects, toxic effects for reproduction.
The health effects of a preparation are to be assessed in accordance with Article 6(1)(a) by the conventional method described in parts A and B of this Annex using individual concentration limits.
where the dangerous substances listed in Annex I to Directive 67/548/EEC are assigned concentration limits necessary for the application of the method of assessment described in part A of this Annex, these concentration limits must be used;
where the dangerous substances do not appear in Annex I to Directive 67/548/EEC or appear there without the concentration limits necessary for the application of the method of evaluation described in part A of this Annex, the concentration limits must be assigned in accordance with the specifications in part B of this Annex.
The procedure for classification is set out in Part A of this Annex.
The classification of the substance(s) and the resulting classification of the preparation are expressed:
either by a symbol and one or more risk phrases, or
by categories (category 1, category 2 or category 3) also assigned risk phrases when substances and preparations are shown to be carcinogenic, mutagenic or toxic for reproduction. Therefore it is important to consider, in addition to the symbol, all the phrases denoting specific risks which are assigned to each substance under consideration.
The systematic assessment of all the dangerous health effects is expressed by means of concentration limits, expressed as a weight/weight percentage except for gaseous preparations where they are expressed as a volume/volume percentage and in conjunction with the classification of the substance.
Where they are not given in Annex I to Directive 67/548/EEC, the concentration limits to be taken into account for the application of this conventional method are those set out in Part B of this Annex.
The evaluation proceeds stepwise as follows:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 1 in Part B of this Annex (Table I and I A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each very toxic substance in the preparation,
=
is the very toxic limit specified for each very toxic substance, expressed as a percentage by weight or by volume;
Preparations containing at least one dangerous substance that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 2 in Part B of this Annex (Table II and II A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 1 in Part B of this Annex (Table I and I A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Where:
=
is the percentage by weight or by volume of each very toxic substance in the preparation,
=
is the percentage by weight or by volume of each toxic substance in the preparation,
=
is the respective toxic limit specified for each very toxic or toxic substance, expressed as a percentage by weight or by volume;
Preparations containing at least one dangerous substance classified as very toxic or toxic that produce such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 2 in Part B of this Annex (Table II and II A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one dangerous substance that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 3 in Part B of this Annex (Table III and III A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 1 in Part B of this Annex (Table I and I A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
Where:
=
is the percentage by weight or by volume of each very toxic substance in the preparation,
=
is the percentage by weight or by volume of each toxic substance in the preparation,
=
is the percentage by weight or by volume of each harmful substance in the preparation,
=
is the respective harmful limit specified for each very toxic, toxic or harmful substance, expressed as percentage by weight or by volume;
Preparations classified as harmful according to the criteria specified in paragraph 3.2.3 of Annex VI to Directive 67/548/EEC. In applying the conventional method according to the above paragraph 3.1 no account shall be taken of the classification of a substance as R65;
Preparations containing at least one dangerous substance classified as very toxic, toxic or harmful that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 2 in Part B of this Annex (Table II and II A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Textual Amendments
F1 Substituted by Commission Directive 2001/60/EC of 7 August 2001 adapting to technical progress Directive 1999/45/EC of the European Parliament and of the Council concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (Text with EEA relevance).
Preparations containing at least one dangerous substance classified as toxic or harmful that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 3 in Part B of this Annex (Table III and III A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
where:
=
is the percentage by weight or by volume of each corrosive substance which is assigned phrase R35 in the preparation,
=
is the corrosive limit R35 specified for each corrosive substance to which is assigned phrase R35, expressed as a percentage by weight or by volume;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R35 in the preparation,
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R34 in the preparation,
=
is the respective corrosive limit R34 specified for each corrosive substance to which is assigned phrase R35 or R34, expressed as a percentage by weight or by volume.
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R35 in the preparation,
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R34 in the preparation,
=
is the percentage by weight or by volume of each irritant substance to which is assigned phrase R41 in the preparation,
=
is the respective irritant limit R41 specified for each corrosive substance to which is assigned phrase R35 or R34 or irritant substance to which is assigned phrase R41, expressed as percentage by weight or by volume;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R35 in the preparation,
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R34 in the preparation,
=
is the percentage by weight or by volume of each irritant substance to which is assigned phrase R41 in the preparation,
=
is the percentage by weight or by volume of each irritant substance to which is assigned phrase R36 in the preparation,
=
is the respective irritant limit R36 specified for each corrosive substance to which is assigned phrase R35 or R34 or irritant substance to which is assigned phrase R41, or R36 expressed as percentage by weight or by volume;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R35 in the preparation,
=
is the percentage by weight or by volume of each corrosive substance to which is assigned phrase R34 in the preparation,
=
is the percentage by weight or by volume of each irritant substance to which is assigned phrase R38 in the preparation,
=
is the respective irritant limit R38 specified for each corrosive substance to which is assigned phrase R35 or R34 or irritant substance to which is assigned phrase R38, expressed as percentage by weight or by volume;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 4 in Part B of this Annex (Table IV and IV A) where the substance or the substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight or by volume of each irritant substance to which is assigned phrase R37 in the preparation,
=
is the irritant limit R37 specified for each irritant substance to which is assigned phrase R37, expressed as percentage by weight or by volume;
where:
=
is the percentage by volume of each corrosive substance to which is assigned phrase R35 in the preparation,
=
is the percentage by volume of each corrosive substance to which is assigned phrase R34 in the preparation,
=
is the percentage by volume of each irritant substance to which is assigned phrase R37 in the preparation,
=
is the respective irritant limit R37 specified for each gaseous corrosive substance to which is assigned phrase R35 or R34 or gaseous irritant substance to which is assigned phrase R37, expressed as percentage by weight or by volume.
Preparations containing at least one substance classified as sensitising and to which is assigned phrase R43 that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 5 in Part B of this Annex (Table V and V A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance classified as sensitising to which is assigned phrase R42 that produces such effects in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 5 in Part B of this Annex (Table V and V A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
Preparations containing at least one substance producing such effects, classified as carcinogenic and to which is assigned phrase R45 or R49 which denotes carcinogenic substances in category 1 and category 2, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance producing such effects classified as carcinogenic and to which is assigned phrase R40 which denotes carcinogenic substances in category 3, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
Preparations containing at least one substance producing such effects, classified as mutagenic and to which is assigned phrase R46 which denotes mutagenic substances in category 1 and category 2, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance, producing such effects, classified as mutagenic and to which is assigned phrase R68] which denotes mutagenic substances in category 3, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
Preparations containing at least one substance producing such effects, classified as toxic for reproduction and to which is assigned phrase R60 which denotes substances toxic for reproduction of category 1 and category 2, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance producing such effects, classified as toxic for reproduction and to which is assigned phrase R62 which denotes substances toxic for reproduction of category 3, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance producing such effects, classified as toxic for reproduction and to which is assigned phrase R61 which denotes substances toxic for reproduction of category 1 and category 2, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
Preparations containing at least one substance producing such effects, classified as toxic for reproduction and to which is assigned phrase R63 which denotes substances toxic for reproduction of category 3, in individual concentrations equal to or greater than:
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified at point 6 in Part B of this Annex (Table VI and VI A) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits.
For each health effect, the first table (Tables I to VI) sets out the concentration limits (expressed as a weight/weight percentage) to be used for non-gaseous preparations and the second table (Tables I A to VI A) sets out the concentration limits (expressed as a volume/volume percentage) to be used for gaseous preparations. These concentration limits are used in the absence of specific concentration limits for the substance under consideration in Annex I to Directive 67/548/EEC.
The concentration limits fixed in Table I, expressed as a weight/weight percentage, determine the classification of the preparation in relation to the individual concentration of the substance(s) present whose classification is also shown.
Table I | |||
Classification of the substance | Classification of the preparation | ||
---|---|---|---|
T+ | T | Xn | |
T+ with R26, R27, R28 | concentration ≥ 7 % | 1 % ≤ concentration < 7 % | 0,1 % ≤ concentration < 1 % |
T with R23, R24, R25 | concentration ≥ 25 % | 3 % ≤ concentration < 25 % | |
Xn with R20, R21, R22 | concentration ≥ 25 % |
The R phrases denoting risk are to be assigned to the preparation in accordance with the following criteria:
the label shall include one or more of the abovementioned R phrases according to the classification used,
in general, the R phrases selected should be those applicable to the substance(s) present in the concentration which gives rise to the most severe classification.
The concentration limits expressed as a volume/volume percentage in Table I A below determine the classification of the gaseous preparations in relation to the individual concentration of the gas(es) present whose classification is also shown.
Table I A | |||
Classification of the substance(gas) | Classification of the gaseous preparation | ||
---|---|---|---|
T+ | T | Xn | |
T+ with R26, R27, R28 | concentration ≥ 1 % | 0,2 % ≤ concentration < 1 % | 0,02 % ≤ concentration < 0,2 % |
T with R23, R24, R25 | concentration ≥ 5 % | 0,5 % ≤ concentration < 5 % | |
Xn with R20, R21, R22 | concentration ≥ 5 % |
The R phrases denoting risk shall be assigned to the preparation in accordance with the following criteria:
the label shall include one or more of the abovementioned R phrases according to the classification used,
in general, the R phrases selected should be those applicable to the substance(s) present in the concentration which gives rise to the most severe classification.
For substances that produce non-lethal irreversible effects after a single exposure (R39/route of exposure, [F1R68/route of exposure), the individual concentration limits specified in Table II, expressed as a weight/weight percentage, determine, when appropriate, the classification of the preparation.
Table II | |||
a In order to indicate the route of administration/exposure (route of exposure) the combined R phrases listed under points 3.2.1, 3.2.2 and 3.2.3 of the labelling guide (Annex VI to Directive 67/548/EEC) are to be used. | |||
Classification of the substance | Classification of the preparation | ||
---|---|---|---|
T+ | T | Xn | |
T+ with R39/route of exposure | concentration ≥ 10 % R39a obligatory | 1 % ≤ concentration < 10 % R39a obligatory | 0,1 % ≤ concentration < 1 % R68 a obligatory |
T with R39/route of exposure | concentration ≥ 10 % R39a obligatory | 1 % ≤ concentration < 10 % R68 a obligatory | |
Xn with R68/route of exposure | concentration ≥ 10 % R68] a obligatory |
For gases that produce non-lethal irreversible effects after a single exposure (R39/route of exposure, [F1R68/route of exposure), the individual concentration limits specified in Table II A, expressed as a volume/volume percentage, determine, when appropriate, the classification of the preparation.
Table II A | |||
a In order to indicate the route of administration/exposure (route of exposure) the combined R phrases listed under points 3.2.1, 3.2.2 and 3.2.3 of the labelling guide (Annex VI to Directive 67/548/EEC) are to be used. | |||
Classification of the substance (gas) | Classification of the gaseous preparation | ||
---|---|---|---|
T+ | T | Xn | |
T+ with R39/route of exposure | concentration ≥ 1 % R39a obligatory | 0,2 % ≤ concentration < 1 % R39a obligatory | 0,02 % ≤ concentration < 0,2 % R68 a obligatory |
T with R39/route of exposure | concentration ≥ 5 % R39a obligatory | 0,5 % ≤ concentration < 5 % R68 a obligatory | |
Xn with R68/route of exposure | concentration ≥ 5 % R68] a obligatory |
For substances that produce severe effects after repeated or prolonged exposure (R 48/route of exposure), the individual concentration limits specified in Table III, expressed as a weight/weight percentage, determine, when appropriate, the classification of the preparation.
Table III | ||
a In order to indicate the route of administration/exposure (route of exposure) the combined R phrases listed under points 3.2.1, 3.2.2 and 3.2.3 of the labelling guide (Annex VI to Directive 67/548/EEC) are to be used. | ||
Classification of the substance | Classification of the preparation | |
---|---|---|
T | Xn | |
T with R48/route of exposure | concentration ≥ 10 % R48a obligatory | 1 % ≤ concentration < 10 % R48a obligatory |
Xn with R48/route of exposure | concentration ≥ 10 % R48a obligatory |
For gases that produce severe effects after repeated or prolonged exposure (R48/route of exposure), the individual concentration limits specified in Table III A below, expressed as a volume/volume percentage, determine, when appropriate, the classification of the preparation.
Table III A | ||
a In order to indicate the route of administration/exposure (route of exposure) the combined R phrases listed under points 3.2.1, 3.2.2 and 3.2.3 of the labelling guide (Annex VI to Directive 67/548/EEC) are to be used. | ||
Classification of the substance(gas) | Classification of the gaseous preparation | |
---|---|---|
T | Xn | |
T with R48/route of exposure | concentration ≥ 5 % R48a obligatory | 0,5 % ≤ concentration < 5 % R48a obligatory |
Xn with R48/route of exposure | concentration ≥ 5 % R48a obligatory |
For substances that produce corrosive effects (R34, R35) or irritant effects (R36, R37, R38, R41), the individual concentration limits specified in Table IV, expressed as a weight/weight percentage, determine, when appropriate, the classification of the preparation.
Table IV | ||||
a According to the labelling guide (Annex VI to Directive 67/548/EEC), corrosive substances assigned risk phrases R35 or R34 must also be considered as being assigned phrase R41. Consequently, if the preparation contains corrosive substances with R35 or R34 below the concentration limits for a classification of the preparation as corrosive, such substances can contribute to a classification of the preparation as irritant with R41 or irritant with R36. | ||||
[F2NB: Simple application of the conventional method to preparations containing substances classified as corrosive or irritant may result in under-classification or over-classification of the hazard, if other relevant factors (e.g. pH of the preparation) are not taken into account. Therefore, in classifying for corrosivity, consider the advice given in paragraph 3.2.5 of Annex VI to Directive 67/548/EEC and in the second and third indents of Article 6(3), of this Directive.] | ||||
Classification of the substance | Classification of the preparation | |||
---|---|---|---|---|
C with R35 | C with R34 | Xi with R41 | Xi with R36, R37, R38 | |
C with R35 | concentration ≥ 10 % R35 obligatory | 5 % ≤ concentration < 10 % R34 obligatory | 5 %a | 1 % ≤ concentration < 5 % R36/38 obligatory |
C with R34 | concentration ≥ 10 % R34 obligatory | 10 %a | 5 % ≤ concentration < 10 % R36/38 obligatory | |
Xi with R41 | concentration ≥ 10 % R41 obligatory | 5 % ≤ concentration < 10 % R36 obligatory | ||
Xi with R36, R37, R38 | concentration ≥ 20 % R36, R37, R38 are obligatory in the light of the concentration present if they apply to the substances under consideration |
For gases that produce such effects (R34, R35 or R36, R37, R38, R41), the individual concentration limits specified in Table IV A below, expressed as a volume/volume percentage determine, when appropriate, the classification of the preparation.
Table IV A | ||||
a According to the labelling guide (Annex VI to Directive 67/548/EEC), corrosive substances assigned risk phrases R35 or R34 must also be considered as being assigned phrase R41. Consequently, if the preparation contains corrosive substances with R35 or R34 below the concentration limits for a classification of the preparation as corrosive, such substances can contribute to a classification of the preparation as irritant with R41 or irritant with R36. | ||||
[F2NB: Simple application of the conventional method to preparations containing substances classified as corrosive or irritant may result in under-classification or over-classification of the hazard, if other relevant factors (e.g. pH of the preparation) are not taken into account. Therefore, in classifying for corrosivity, consider the advice given in paragraph 3.2.5 of Annex VI to Directive 67/548/EEC and in the second and third indents of Article 6(3), of this Directive.] | ||||
Classification of the substance(gas) | Classification of the gaseous preparation | |||
---|---|---|---|---|
C with R35 | C with R34 | Xi with R41 | Xi with R36, R37, R38 | |
C with R35 | concentration ≥ 1 % R35 obligatory | 0,2 % ≤ concentration < 1 % R34 obligatory | 0,2%a | 0,02 % ≤ concentration < 0,2 % R36/37/38 obligatory |
C with R34 | concentration ≥ 5 % R34 obligatory | 5 %a | 0,5 % ≤ concentration < 5 % R36/37/38 obligatory | |
Xi with R41 | concentration ≥ 5 % R41 obligatory | 0,5 % ≤ concentration < 5 % R36 obligatory | ||
Xi with R36, R37, R38 | concentration ≥ 5 % R36, R37, R38 obligatory as appropriate |
Preparations that produce such effects are classified as sensitising and assigned:
the symbol Xn and phrase R42 if this effect can be produced by inhalation,
the symbol Xi and phrase R43 if this effect can be produced through contact with the skin.
The individual concentration limits specified in Table V, expressed as a weight/weight percentage, determine, when appropriate, the classification of the preparation.
Table V | ||
Classification of the substance | Classification of the preparation | |
---|---|---|
Sensitising with R42 | Sensitising with R43 | |
Sensitising with R42 | concentration ≥ 1 % R42 obligatory | |
Sensitising with R43 | concentration ≥ 1 % R43 obligatory |
Gaseous preparations that produce such effects are classified as sensitising and assigned:
the symbol Xn and phrase R42 if this effect can be produced by inhalation,
the symbol Xi and phrase R43 if this effect can be produced through contact with the skin.
The individual concentration limits specified in Table V A below, expressed as a volume/volume percentage, determine, when appropriate, the classification of the preparation.
Table V A | ||
Classification of the substance(gas) | Classification of the gaseous preparation | |
---|---|---|
Sensitising with R42 | Sensitising with R43 | |
Sensitising with R42 | concentration ≥ 0,2 % R42 obligatory | |
Sensitising with R43 | concentration ≥ 0,2 % R43 obligatory |
For substances which produce such effects, the concentration limits laid down in Table VI, expressed as a weight/weight percentage, shall determine, where appropriate, the classification of the preparation. The following symbol and risk phrases are assigned:
Carcinogenic categories 1 and 2: | T; R45 or R49 |
Carcinogenic category 3: | Xn; R40 |
Mutagenic categories 1 and 2: | T; R46 |
Mutagenic category 3: | Xn; [F1R68] |
Toxic for reproduction fertility categories 1 and 2: | T; R60 |
Toxic for reproduction development categories 1 and 2: | T; R61 |
Toxic for reproduction fertility category 3: | Xn; R62 |
Toxic for reproduction development category 3: | Xn; R63 |
a In cases where the preparation is assigned R49 and R40, both R phrases shall be kept, because R40 does not distinguish between the exposure routes, whereas R49 is only assigned for the inhalation route.] | ||
Classification of the substance | Classification of the preparation | |
---|---|---|
Categories 1 and 2 | Category 3 | |
Carcinogenic substances of category 1 or 2 with R45 or R49 | Concentration ≥ 0,1 % carcinogenic R45, R49 obligatory as appropriate | |
Carcinogenic substances of category 3 with R40 | Concentration ≥ 1 % carcinogenic R40 obligatory ( unless already assigned R45 a ) | |
Mutagenic substances of category 1 or 2 with R46 | Concentration ≥ 0,1 % mutagenic R46 obligatory | |
Mutagenic substances of category 3 with R68 | Concentration ≥ 1 % mutagenic R68 obligatory ( unless already assigned R46 ) | |
Substances ‘ toxic for reproduction ’ of category 1 or 2 with R60 (fertility) | Concentration ≥ 0,5 % toxic for reproduction (fertility) R60 obligatory | |
Substances ‘ toxic for reproduction ’ of category 3 with R62 (fertility) | Concentration ≥ 5 % toxic for reproduction (fertility) R62 obligatory ( unless already assigned R60 ) | |
Substances ‘ toxic for reproduction ’ of category 1 or 2 with R61 (development) | Concentration ≥ 0,5 % toxic for reproduction (development) R61 obligatory | |
Substances ‘ toxic for reproduction ’ of category 3 with R63 (development) | Concentration ≥ 5 % toxic for reproduction (development) R63 obligatory ( unless already assigned R61 ) |
Textual Amendments
F3 Substituted by Commission Directive 2006/8/EC of 23 January 2006 amending, for the purposes of their adaptation to technical progress, Annexes II, III and V to Directive 1999/45/EC of the European Parliament and of the Council concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (Text with EEA relevance).
For gases which produce such effects, the concentration limits laid down in Table VI A, expressed as a volume/volume percentage, shall determine, where appropriate, the classification of the preparation. The following symbol and risk phrases are assigned:
Carcinogenic categories 1 and 2: | T; R45 or R49 |
Carcinogenic category 3: | Xn; R40 |
Mutagenic categories 1 and 2: | T; R46 |
Mutagenic category 3: | Xn; [F1R68] |
Toxic for reproduction fertility categories 1 and 2: | T; R60 |
Toxic for reproduction development categories 1 and 2: | T; R61 |
Toxic for reproduction fertility category 3: | Xn; R62 |
Toxic for reproduction development category 3: | Xn; R63 |
a In cases where the preparation is assigned R49 and R40, both R phrases shall be kept, because R40 does not distinguish between the exposure routes, whereas R49 is only assigned for the inhalation route.] | ||
Classification of the substance | Classification of the preparation | |
---|---|---|
Categories 1 and 2 | Category 3 | |
Carcinogenic substances of category 1 or 2 with R45 or R49 | Concentration ≥ 0,1 % carcinogenic R45, R49 obligatory as appropriate | |
Carcinogenic substances of category 3 with R40 | Concentration ≥ 1 % carcinogenic R40 obligatory ( unless already assigned R45 a ) | |
Mutagenic substances of category 1 or 2 with R46 | Concentration ≥ 0,1 % mutagenic R46 obligatory | |
Mutagenic substances of category 3 with R68 | Concentration ≥ 1 % mutagenic R68 obligatory ( unless already assigned R46 ) | |
Substances ‘ toxic for reproduction ’ of category 1 or 2 with R60 (fertility) | Concentration ≥ 0,2 % toxic for reproduction (fertility) R60 obligatory | |
Substances ‘ toxic for reproduction ’ of category 3 with R62 (fertility) | Concentration ≥ 1 % toxic for reproduction (fertility) R62 obligatory ( unless already assigned R60 ) | |
Substances ‘ toxic for reproduction ’ of category 1 or 2 with R61 (development) | Concentration ≥ 0,2 % toxic for reproduction (development) R61 obligatory | |
Substances ‘ toxic for reproduction ’ of category 3 with R63 (development) | Concentration ≥ 1 % toxic for reproduction (development) R63 obligatory ( unless already assigned R61 ) |
The systematic assessment of all the dangerous properties for the environment is expressed by means of concentration limits, expressed as a weight/weight percentage except for gaseous preparations where they are expressed as a volume/volume percentage and in conjunction with the classification of a substance.
Part A gives the calculation procedure according to Article 7(1)(a) and gives the R phrases to be assigned to the classification of the preparation.
Part B gives the concentration limits to be used when applying the conventional method and relevant symbols and R phrases for classification.
In accordance with Article 7(1)(a) the environmental hazards of a preparation shall be assessed by the conventional method described in parts A and B of this Annex, using individual concentration limits.
Where the dangerous substances listed in Annex 1 to Directive 67/548/EEC are assigned concentration limits necessary for the application of the method of assessment described in Part A of this Annex, these concentration limits must be used.
Where the dangerous substances do not appear in Annex I to Directive 67/548/EEC or appear there without the concentration limits necessary for the application of the method of evaluation described in Part A of this Annex, the concentration limits shall be assigned in accordance with the specification in Part B of this Annex.
Part C gives the test methods for the evaluation of the hazards for the aquatic environment.
The conventional method for the evaluation of hazards to the aquatic environment [X1takes into account all the hazards that a preparation may entail] for this medium according to the following specifications.
Editorial Information
X1 Substituted by Corrigendum to Directive 1999/45/EC of the European Parliament and of the Council of 31 May 1999 concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (Official Journal of the European Communities L 200 of 30 July 1999).
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 1) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R50-53 in the preparation,
=
is the limit R50-53 for each substance dangerous for the environment to which is assigned the phrases R50-53, expressed as percentage by weight
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 1) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R50-53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R51-53 in the preparation,
=
is the respective limit R51-53 for each substance dangerous for the environment to which is assigned phrases R50-53 or R51-53, expressed as percentage by weight
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 1) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R50-53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R51-53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R52-53 in the preparation,
=
is the respective limit R52-53 for each substance dangerous for the environment to which is assigned phrases R50-53 or R51-53 or R52-53, expressed as percentage by weight;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 2) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R50 in the preparation,
=
is the limit R50 for each substance dangerous for the environment to which is assigned phrase R50, expressed as percentage by weight.
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R50 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrases R50-53 in the preparation,
=
is the perspective limit R50 for each substance dangerous for the environment to which is assigned phrases R50 or R50-53, expressed as percentage by weight;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 3) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R52 in the preparation,
=
is the limit R52 for each substance dangerous for the environment to which is assigned phrase R52, expressed as percentage by weight;
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 4) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R53 in the preparation,
=
is the limit R53 for each substance dangerous for the environment to which is assigned phrase R53, expressed as percentage by weight;
where:
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R50-53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R51-53 in the preparation,
=
is the percentage by weight of each substance dangerous for the environment to which is assigned phrase R52-53 in the preparation,
=
is the respective limit R53 for each substance dangerous for the environment to which is assigned phrase R53 or R50-53 or R51-53 or R52-53, expressed as percentage by weight.
either the concentration specified in Annex I to Directive 67/548/EEC for the substance or substances under consideration, or
the concentration specified in Part B of this Annex (Table 5) where the substance or substances do not appear in Annex I to Directive 67/548/EEC or appear in it without concentration limits[F3.]
Textual Amendments
F4 Deleted by Commission Directive 2006/8/EC of 23 January 2006 amending, for the purposes of their adaptation to technical progress, Annexes II, III and V to Directive 1999/45/EC of the European Parliament and of the Council concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (Text with EEA relevance).
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Classification of preparations using the risk phrases below will follow after the detailed criteria for use of the phrases have been incorporated in Annex VI to Directive 67/548/EEC.
Toxic to flora
Toxic to fauna
Toxic to soil organisms
Toxic to bees
May cause long-term adverse effects in the environment.
The concentration limits fixed in the following tables, expressed as a weight/weight percentage, determine the classification of the preparation in relation to the individual concentration of the substance(s) present whose classification is also shown.
Acute aquatic toxicity and long-term adverse effects
Classification of the substance | Classification of the preparation | ||
---|---|---|---|
N, R50-53 | N, R51-53 | R52-53 | |
N, R50-53 | see Table 1b | see Table 1b | see Table 1b |
N, R51-53 | C n ≥ 25 % | 2,5 % ≤ C n < 25 % | |
R52-53 | C n ≥ 25 % |
Preparations containing a substance classified with N, R50-53, the concentration limits and the resulting classification given in table 1b are applicable.
Acute aquatic toxicity and long-term adverse effects of substances very toxic to the aquatic environment
For preparations containing substances with a lower LC 50 or EC 50 value than 0,00001 mg/l, the corresponding concentration limits are calculated accordingly (in factor 10 intervals).] | |||
LC 50 or EC 50 value (‘L(E)C 50 ’) of substance classified as N, R50-53 (mg/l) | Classification of the preparation | ||
---|---|---|---|
N, R50-53 | N, R51-53 | R52-53 | |
0,1 < L(E)C 50 ≤ 1 | C n ≥ 25 % | 2,5 % ≤ C n < 25 % | 0,25 % ≤ C n < 2,5 % |
0,01 < L(E)C 50 ≤ 0,1 | C n ≥ 2,5 % | 0,25 % ≤ C n < 2,5 % | 0,025 % ≤ C n < 0,25 % |
0,001 < L(E)C 50 ≤ 0,01 | C n ≥ 0,25 % | 0,025 % ≤ C n < 0,25 % | 0,0025 % ≤ C n < 0,025 % |
0,0001 < L(E)C 50 ≤ 0,001 | C n ≥ 0,025 % | 0,0025 % ≤ C n < 0,025 % | 0,00025 % ≤ C n < 0,0025 % |
0,00001 < L(E)C 50 ≤ 0,0001 | C n ≥ 0,0025 % | 0,00025 % ≤ C n < 0,0025 % | 0,000025 % ≤ C n < 0,00025 % |
Acute aquatic toxicity
For preparations containing substances with a lower LC 50 or EC 50 value than 0,00001 mg/l, the corresponding concentration limits are calculated accordingly (in factor 10 intervals).] | |
LC 50 or EC 50 value (‘L(E)C 50 ’) of substance classified either as N, R50 or as N, R50-53 (mg/l) | Classification of the preparation N, R50 |
---|---|
0,1 < L(E)C 50 ≤ 1 | C n ≥ 25 % |
0,01 < L(E)C 50 ≤ 0,1 | C n ≥ 2,5 % |
0,001 < L(E)C 50 ≤ 0,01 | C n ≥ 0,25 % |
0,0001 < L(E)C 50 ≤ 0,001 | C n ≥ 0,025 % |
0,00001 < L(E)C 50 ≤ 0,0001 | C n ≥ 0,0025 % |
Table 3 | |
Aquatic toxicity | |
Classification of the substance | Classification of the preparation R52R52 |
---|---|
R52 | Cn ≥ 25 % |
Table 4 | |
Long-term adverse effects | |
Classification of the substance | Classification of the preparation R53R53 |
---|---|
R53 | Cn ≥ 25 % |
N, R50—53 | Cn ≥ 25 % |
N, R51—53 | Cn ≥ 25 % |
R52—53 | Cn ≥ 25 % |
The concentration limits fixed in the following tables, expressed as weight/weight percentage or, for gaseous preparations as a volume/volume percentage, determine the classification of the preparation in relation to the individual concentration of the substance(s) present whose classification is also shown.
Dangerous for the ozone layer
Classification of the substance | Classification of the preparation N, R59 |
---|---|
N with R59 | C n ≥ 0,1 %] |
Normally, the classification of a preparation is made on the basis of the conventional method. However, for the determination of the acute aquatic toxicity, there may be cases for which it is appropriate to carry out tests on the preparation.
The result of these tests on the preparation may only modify the classification concerning acute aquatic toxicity which would have been obtained by the application of the conventional method.
If such tests are chosen by the person responsible for the placing on the market, it must be ensured that the quality criteria of the test methods in Part C of Annex V to Directive 67/548/EEC have been complied with.
Furthermore, the tests are to be carried out on all three species in conformity with the criteria of Annex VI to Directive 67/548/EEC (algae, daphnia and fish), unless the highest hazard classification relating to acute aquatic toxicity has been assigned to the preparation after testing on one of the species or a test result was already available before this Directive entered into force.
No | Identification of the substance | Concentration limit | ||
---|---|---|---|---|
CAS-Reg No | Name | Einecs No | ||
1 | 67-56-1 | Methanol | 2006596 | ≥ 3 % |
2 | 75-09-2 | Dichloromethane | 2008389 | ≥ 1 % |
which are offered or sold to the general public are to be fitted with child-resistant fastenings.
Containers of whatever capacity, containing preparations offered or sold to the general public and labelled as very toxic, toxic, corrosive, harmful, extremely flammable or highly flammable in accordance with Article 10 and under the conditions laid down in Articles 5 and 6 of this Directive, are to carry a tactile warning of danger.
This provision does not apply to aerosols classified and labelled only as extremely flammable or highly flammable.
The label on the packaging containing such preparations must compulsorily bear the safety advice S23 accompanied by safety advice S38 or S51 assigned to it in accordance with the criteria laid down in Annex VI to Directive 67/548/EEC.
When a preparation contains at least one substance assigned the phrase R33, the label on the packaging of the preparation must carry the wording of this phrase as set out in Annex III to Directive 67/548/EEC, when the concentration of this substance present in the preparation is equal to or higher than 1 %, unless different values are set in Annex I to Directive 67/548/EEC.
When a preparation contains at least one substance assigned phrase R64, the label on the packaging of the preparation must carry the wording of this phrase as set out in Annex III to Directive 67/548/EEC, when the concentration of this substance present in the preparation is equal to or higher than 1 %, unless different values are set in Annex I to Directive 67/548/EEC.
The label on the packaging of paints and varnishes containing lead in quantities exceeding 0,15 % (expressed as weight of metal) of the total weight of the preparation, as determined in accordance with ISO standard 6503/1984, must show the following particulars:
‘ Contains lead. Should not be used on surfaces liable to be chewed or sucked by children ’ .
In the case of packages the contents of which are less than 125 millilitres, the particulars may be as follows:
‘ Warning! Contains lead ’ .
The label on the immediate packaging of adhesives based on cyanoacrylate must bear the following inscriptions:
‘Cyanoacrylate
Danger
Bonds skin and eyes in seconds
Keep out of the reach of children’ .
Appropriate advice on safety must accompany the package.
The label on the packaging of preparations containing isocyanates (as monomers, oligomers, prepolymers, etc., or as mixtures thereof) must bear the following inscriptions:
‘Contains isocyanates.
See information supplied by the manufacturer’ .
The label on the packaging of preparations containing epoxy constituents with an average molecular weight ≤ 700 must bear the following inscriptions:
‘Contains epoxy constituents.
See information supplied by the manufacturer’ .
The label on the packaging of preparations containing more than 1 % of active chlorine must bear the following particular inscriptions:
‘ Warning! Do not use together with other products. May release dangerous gases (chlorine) ’ .
The label on the packaging of the above mentioned preparations must bear the following inscription printed in clearly legible and indelible characters:
‘Warning! Contains cadmium.
Dangerous fumes are formed during use.
See information supplied by the manufacturer.
Comply with the safety instructions’ .
Without prejudice to the provisions of this Directive, preparations available as aerosols are also subject to the labelling provisions in accordance with points 2.2 and 2.3 of the Annex to Directive 75/324/EEC as last amended by Directive 94/1/EC.
Where a preparation contains at least one substance which, in accordance with Article 13.3 of Directive 67/548/EEC, bears the inscription ‘ [X2Caution — substance not yet fully tested ’ ,] the label on the packaging of the preparation must bear the inscription ‘Warning — this preparation contains a substance not yet tested completely’ if this substance is present in a concentration ≥ 1 %.
Editorial Information
X2 Substituted by Corrigendum to Commission Directive 2006/8/EC of 23 January 2006 amending, for the purposes of their adaptation to technical progress, Annexes II, III and V to Directive 1999/45/EC of the European Parliament and of the Council concerning the approximation of the laws, regulations and administrative provisions of the Member States relating to the classification, packaging and labelling of dangerous preparations (Official Journal of the European Union L 19 of 24 January 2006).
The label on the packaging of preparations containing at least one substance classified as sensitising and being present in a concentration equal to or greater than 0,1 % or in a concentration equal to or greater than that specified under a specific note for the substance in Annex I to Directive 67/548/EEC must bear the inscription:
‘ Contains (name of sensitising substance). May produce an allergic reaction ’ .
For liquid preparations which show no flashpoint or a flashpoint higher than 55 °C and contain a halogenated hydrocarbon and more than 5 % flammable or highly flammable substances, the label on the packaging must bear the following inscription as appropriate:
‘ Can become highly flammable in use ’ or ‘ Can become flammable in use ’ .
When a preparation contains one or more substances assigned the phrase R67, the label on the packaging of the preparation must carry the wording of this phrase as set out in Annex III to Directive 67/548/EEC, when the total concentration of these substances present in the preparation is equal to or higher than 15 %, unless:
the preparation is already classified with phrases R20, R23, R26, R68/20, R39/23 or R39/26,
or the preparation is in a package not exceeding 125 ml.
The label on the packaging of cements and cement preparations containing more than 0,0002 % soluble chromium (VI) of the total dry weight of the cement must bear the inscription:
‘ Contains chromium (VI). May produce an allergic reaction ’
unless the preparation is already classified and labelled as a sensitiser with phrase R43.
The label on the packaging of preparations referred to in Article 14.2.1(b) must bear the following inscription:
‘ Safety data sheet available for professional user on request ’ .]
Article 15 indicates the conditions in which the person responsible for placing a preparation on the market may avail himself of the confidentiality.
To avoid multiple requests for confidentiality relating to the same substance used in different preparations, a single request for confidentiality may suffice if a certain number of preparations have:
the same dangerous constituents present in the same concentration range,
the same classification and labelling,
the same expected uses.
A single alternative denomination must be used to mask the chemical identity of the same substance in the preparations concerned. Furthermore, the request for confidentiality must contain all information indicated in the following request, without forgetting the name or the trade name of each preparation.
The alternative designation used on the label must be the same as that given under heading 2 ‘Composition/information on ingredients’ of the Annex to Directive 91/155/EEC as last amended by Directive 93/112/EEC.
This implies that the alternative designation used will contain enough information about the substance to ensure risk-free handling.
In making the request to use an alternative designation the person responsible for placing on the market must take into account the need to provide enough information for necessary health and safety precautions to be taken in the workplace and to ensure that risks from handling the preparation can be minimised.
In accordance with Article 15 the request for confidentiality must obligatorily contain the following information:
Name and full address (including telephone number) of the person established in the Community who is responsible for placing the preparation on the market (manufacturer, importer or distributor).
Precise identification of the substance(s) for which confidentiality is proposed and the alternative designation.
NB: Where substances are classified provisionally, accompanying information (bibliographical references) should be provided as evidence that the provisional classification takes account of all existing pertinent information available on the properties of the substance. | |||
CAS No | Einecs No | Chemical name according to international nomenclature and classification (Annex I to Council Directive 67/548/EEC or provisional classification) | Alternative designation |
---|---|---|---|
(a) | |||
(b) | |||
(c) |
Justification for confidentiality (probability — plausibility).
Designation(s) or commercial name(s) of the preparation(s).
Is the designation or commercial name the same for all the Community?
YES | NO |
If no, specify the designation(s) or commercial name(s) used in the different Member States:
[F5Belgium:
Bulgaria:
Czech Republic:
Denmark:
Germany:
Estonia:
Greece:
Spain:
France:
Ireland:
Italy:
Cyprus:
Latvia:
Lithuania:
Luxembourg:
Hungary:
Malta:
Netherlands:
Austria:
Poland:
Portugal:
Romania:
Slovenia:
Slovakia:
Finland:
Sweden:
United Kingdom:]
Composition of the preparation(s) defined in point 2 of the Annex to Directive 91/155/EEC as last amended by Directive 93/112/EEC.
Classification of the preparation(s) according to Article 6 of this Directive.
Labelling of the preparation(s) according to Article 10 of this Directive.
Intended uses for the preparation(s).
Safety data sheet(s) conforming to Directive 91/155/EEC as last amended by Directive 93/112/EEC.
Textual Amendments
The lexicon guide is based on the procedure for the classification of dangerous substances (division of substances into families) which appears in Annex I to Directive 67/548/EEC.
Alternative designations to those based on this guide may be used. However, in all cases the names chosen must provide enough information to ensure the preparation can be handled without risk and that necessary health and safety precautions can be taken in the workplace.
The families are defined in the following manner:
inorganic or organic substances whose properties are identified by having a common chemical element as their chief characteristic. The family name is derived from the name of the chemical element. These families are identified as in Annex I by the atomic number of the chemical element (001 to 103),
organic substances whose properties are identified by having a common functional group as their chief characteristics.
The family name is derived from the functional group name.
These families are identified by the conventional number found in Annex I (601—650).
Sub-families bringing together substances with a common specific character have been added in certain cases.
General principles
For the purposes of establishing the generic name, the following general approach, involving two successive stages, is adopted:
identification of the functional groups and chemical elements present in the molecule;
determination of the extent to which account should be taken of the most important functional groups and chemical elements.
The identified functional groups and elements taken into account are the names of the families and sub-families set out in point 3 in the form of a non-restrictive list.
a Specify according to the family corresponding to halogen. | |
b Quinones included. | |
Family NoAnnex I to Directive 67/548/EEC | FamiliesSub-families |
---|---|
001 | Hydrogen compounds Hydrides |
002 | Helium compounds |
003 | Lithium compounds |
004 | Beryllium compounds |
005 | Boron compounds
|
006 | Carbon compounds
|
007 | Nitrogen compounds
|
008 | Oxygen compounds |
009 | Fluorine compounds Inorganic fluorides |
010 | Neon compounds |
011 | Sodium compounds |
012 | Magnesium compounds Organometallic magnesium derivatives |
013 | Aluminium compounds Organometallic aluminium derivatives |
014 | Silicon compounds
|
015 | Phosphorus compounds
|
016 | Sulphur compounds
|
017 | Chlorine compounds
|
018 | Argon compounds |
019 | Potassium compounds |
020 | Calcium compounds |
021 | Scandium compounds |
022 | Titanium compounds |
023 | Vanadium compounds |
024 | Chromium compounds Chromium VI compounds |
025 | Manganese compounds |
026 | Iron compounds |
027 | Cobalt compounds |
028 | Nickel compounds |
029 | Copper compounds |
030 | Zinc compounds Organometallic zinc derivatives |
031 | Gallium compounds |
032 | Germanium compounds |
033 | Arsenic compounds |
034 | Selenium compounds |
035 | Bromine compounds |
036 | Krypton compounds |
037 | Rubidium compounds |
038 | Strontium compounds |
039 | Yttrium compounds |
040 | Zirconium compounds |
041 | Niobium compounds |
042 | Molybdenum compounds |
043 | Technetium compounds |
044 | Ruthenium compounds |
045 | Rhodium compounds |
046 | Palladium compounds |
047 | Silver compounds |
048 | Cadmium compounds |
049 | Indium compounds |
050 | Tin compounds Organometallic tin derivatives |
051 | Antimony compounds |
052 | Tellurium compounds |
053 | Iodine compounds |
054 | Xenon compounds |
055 | Caesium compounds |
056 | Barium compounds |
057 | Lanthanum compounds |
058 | Cerium compounds |
059 | Praseodymium compounds |
060 | Neodymium compounds |
061 | Promethium compounds |
062 | Samarium compounds |
063 | Europium compounds |
064 | Gandolinium compounds |
065 | Terbium compounds |
066 | Dysprosium compounds |
067 | Holmium compounds |
068 | Erbium compounds |
069 | Thulium compounds |
070 | Ytterbium compounds |
071 | Lutetium compounds |
072 | Hafnium compounds |
073 | Tantalum compounds |
074 | Tungsten compounds |
075 | Rhenium compounds |
076 | Osmium compounds |
077 | Iridium compounds |
078 | Platinum compounds |
079 | Gold compounds |
080 | Mercury compounds Organometallic mercury derivatives |
081 | Thallium compounds |
082 | Lead compounds Organometallic lead derivatives |
083 | Bismuth compounds |
084 | Polonium compounds |
085 | Astate compounds |
086 | Radon compounds |
087 | Francium compounds |
088 | Radium compounds |
089 | Actinium compounds |
090 | Thorium compounds |
091 | Protactinium compounds |
092 | Uranium compounds |
093 | Neptunium compounds |
094 | Plutonium compounds |
095 | Americium compounds |
096 | Curium compounds |
097 | Berkelium compounds |
098 | Californium compounds |
099 | Einsteinium compounds |
100 | Fermium compounds |
101 | Mendelevium compounds |
102 | Nobelium compounds |
103 | Lawrencium compounds |
601 | Hydrocarbons
|
602 | Halogenated hydrocarbonsa |
603 | Alcohols and derivatives
|
604 | Phenols and derivatives Halogenated phenol derivativesa |
605 | Aldehydes and derivatives
|
606 | Ketones and derivatives
|
607 | Organic acids and derivatives
|
608 | Nitriles and derivatives |
609 | Nitro compounds |
610 | Chlornitrated compounds |
611 | Azoxy and azo compounds |
612 | Amine compounds
|
613 | Heterocyclic bases and derivatives
|
614 | Glycosides and alkaloids
|
615 | Cyanates and isocyanates
|
616 | Amides and derivatives
|
617 | Organic peroxides |
647 | Enzymes |
648 | Complex coal derivatives
|
649 | Complex oil derivatives
|
650 | Various substances Do not use this family. Instead, use the families or sub-families mentioned above. |
After having conducted a search to see if the substance belongs to one or more families or sub-families on the list, the generic name can be established in the following way:
Examples:
1,4 dihydroxybenzen
:
phenols and derivatives
:
phenol derivatives
butanol
:
alcohols and derivatives
:
aliphatic alcohols
:
aliphatic alcohol
2-Isopropoxyethanol
:
alcohols and derivatives
:
glycolethers
:
glycolether
methacrylate
:
organic acids and derivatives
:
acrylates
:
acrylate
Examples:
chlorobenzene
:
halogenated hydrocarbons
:
halogenated aromatic hydrocarbons
:
chlorine compounds
:
chlorinated aromatic hydrocarbon
2,3,6-trichlorophenylacetic acid
:
organic acids
:
halogenated aromatic acids
:
chlorine compounds
:
chlorinated aromatic acid
1-chloro-1-nitropropane
:
chloronitrated derivatives
:
hydrocarbons
:
aliphatic hydrocarbons
:
chlorinated aliphatic hydrocarbon
tetrapropyl dithiopyrophosphate
:
phosphorus compounds
:
phosphoric esters
:
sulphur compounds
:
thiophosphoric ester
In the case of certain elements, notably metals, the name of the family or sub-family may be indicated by the words‘organic’ or ‘inorganic’.
Examples:
dimercury chloride
:
mercury compounds
:
inorganic mercury compound
barium acetate
:
barium compounds
:
organic barium compound
ethyl nitrite
:
nitrogen compounds
:
nitrites
:
organic nitrite
sodium hydrosulphite
:
sulphur compounds
:
inorganic sulphur compound
(The examples cited are substances taken from Annex I to Directive 67/548/EEC (19th adaptation) in respect of which requests for confidentiality may be submitted).
Preparations as specified by paragraph 9.3 of Annex VI to Directive 67/548/EEC.
Directive 78/631/EEC on the approximation of the laws of the Member States relating to the classification, packaging and labelling of dangerous preparations (pesticides)
Directive 88/379/EEC on the approximation of the laws of the Member States relating to the classification, packaging and labelling of dangerous preparations and its following adaptations to technical progress:
Directive 89/178/EEC
Directive 90/492/EEC
Directive 93/18/EEC
Directive 96/65/EC
Directive 90/35/EEC defining in accordance with Article 6 of Directive 88/379/EEC the category of preparations the packaging of which must be fitted with child-resistant fastenings and/or carry a tactile warning of danger
Directive 91/442/EEC on dangerous preparations the packaging of which must be fitted with child-resistant fastenings
Directive | Deadline for transposition | Deadline for application |
---|---|---|
78/631/EEC (OJ L 206, 29.7.1978, p. 13) | 1 January 1981 | 1 January 1981 |
88/379/EEC (OJ L 187, 16.7.1988, p. 14) | 7 June 1991 | 7 June 1991 |
89/178/EEC (OJ L 64, 8.3.1989, p. 18) | 1 December 1990 | 1 June 1991 |
90/492/EEC (OJ L 275, 5.10.1990, p. 35) | 1 June 1991 | 8 June 1991 |
93/18/EEC (OJ L 104, 29.4.1993, p. 46) | 1 July 1994 | 1 July 1994 |
90/35/EEC (OJ L 19, 24.1.1990, p. 14) | 1 August 1992 | 1 November 1992 |
91/442/EEC (OJ L 238, 27.8.1991, p. 25) | 1 August 1992 | 1 November 1992 |
96/65/EC (OJ L 265, 18.10.1996, p. 15) | 31 May 1998 | 31 May 1998 |
The following provisions of Directive 88/379/EEC will not apply to Austria
Article 13 in conjunction with Articles 3 and 7 with respect to preparations containing substances listed in Appendix 1;
Article 13 in conjunction with Article 7 with respect to labelling respecting the Austrian provisions on:
safety advice for waste disposal,
pictogram for waste disposal until two years after the entry into force of this Directive,
safety advice for countermeasures in case of accidents;
Article 13 in conjunction with Article 7(1)(c) concerning the chemical names of dangerous substances present in dangerous preparations, until two years after the entry into force of this Directive.
The following provisions of Directive 88/379/EEC will not apply to Sweden:
Article 13 in conjunction with Articles 3 and 7 with respect to preparations
containing substances listed in Appendix 2,
containing substances presenting neurotoxic effects and defatting effects on the skin not covered by criteria for classification of Annex VI to Directive 67/548/EEC, and by risk phrases of Annex III to Directive 67/548/EEC,
containing substances presenting acutely toxic effects not covered by criteria for classification of Annex VI to Directive 67/548/EEC, and by risk phrases of Annex III to Directive 67/548/EEC, until two years after the entry into force of this Directive,
which are not classified as dangerous according to the ‘måttligt skadliga’ (Swedish: ‘moderately harmful’) criteria of Directive 88/379/EEC.
Article 13 in conjunction with Articles 3 and 7 with respect to
the criteria for classification and labelling of preparations containing carcinogenic substances classified on the basis of criteria in point 4.2.1 of Annex VI to Directive 67/548/EEC,
labelling of preparations classified as carcinogenic, category 3, with a special R-phrase instead of R-phrase 40.
Name of the substance | Index number in Annex I to Directive 67/548/EEC |
---|---|
Linuron | 006-021-00-1 |
Trichlorosilan | 014-001-00-9 |
Phosphorus trichloride | 015-007-00-4 |
Phosphorus pentachloride | 015-008-00-X |
Phosphorus oxychloride | 015-009-00-5 |
Sodium polysulphides | 016-010-00-3 |
Disulphur dichloride | 016-012-00-4 |
Thionyl chloride | 016-015-00-0 |
Calcium hypochlorite | 017-012-00-7 |
Potassium hydroxide | 019-002-00-8 |
2-Dimethylaminoethanol | 603-047-00-0 |
2-Diethylaminoethanol | 603-048-00-6 |
Diethanolamine | 603-071-00-1 |
N-Methyl-2-ethanolamine | 603-080-00-0 |
2-Ethylhexan-1,3-diol | 603-087-00-9 |
Isophorone | 606-012-00-8 |
6-Methyl-1,3-dithiolo(4,5-b)chinoxalin-2-one | 606-036-00-9 |
Acetic anhydride | 607-008-00-9 |
Methyl formate | 607-014-00-1 |
Ethyl formate | 607-015-00-7 |
Acrylic acid | 607-061-00-8 |
Chloroacetyl chloride | 607-080-00-1 |
Nitrofen | 609-040-00-9 |
Quintozen; Pentachloronitrobenzol | 609-043-00-5 |
Dichlofluanid | 616-006-00-7 |
Cumene hydroperoxide | 617-002-00-8 |
Monocrotophos | 015-072-00-9 |
Edifenphos | 015-121-00-4 |
Triazophos | 015-140-00-8 |
Methanol | 603-001-00-X |
Trifenmorph; 4-Tritylmorpholin | 613-052-00-X |
Diuron | 006-015-00-9 |
Fenbutanin oxide | 050-017-00-2 |
1-Butanol, 2-Butanol, iso-Butanol | 603-004-00-6 |
Name of the substance | Index number in Annex I to Directive 67/548/EEC |
---|---|
Acetone | 606-001-00-8 |
Butanone | 606-002-00-3 |
Amyl formate | 607-018-00-3 |
Ethyl acetate | 607-022-00-5 |
n-Butylacetate | 607-025-00-1 |
sec-Butylacetate | 607-026-00-7 |
tert-Butylacetate | 607-026-00-7 |
iso-Butylacetate | 607-026-00-7 |
Butylformate | 607-017-00-8 |
Cyclohexane | 601-017-00-1 |
1,4-Dimethylcyclohexane | 601-019-00-2 |
Diethyl ether | 603-022-00-4 |
Ethyl methyl ether | 603-020-00-3 |
Amyl acetate | 607-130-00-2 |
Ethyl lactate | 607-129-00-7 |
Amyl propionate | 607-131-00-8 |
2,4-Dimethylpentan-3-one | 606-028-00-5 |
Di-n-propylether | 603-045-00-X |
Di-n-propyl ketone | 606-027-00-X |
Ethyl propionate | 607-028-00-8 |
Heptane | 601-008-00-2 |
Hexane (mixture of isomers) containing less than 5 % n-hexane | 601-007-00-7 |
Isopropyl acetate | 607-024-00-6 |
Isopropyl alcohol | 603-003-00-0 |
4-Methoxy-4-methylpentane-2-one | 606-023-00-8 |
Methyl acetate | 607-021-00-X |
Methyl cyclohexane | 601-018-00-7 |
5-Methylhexane-2-one | 606-026-00-4 |
Methyllactate | 607-092-00-7 |
4-Methylpentan-2-one | 606-004-00-4 |
Methyl propionate | 607-027-00-2 |
Octane | 601-009-00-8 |
Pentane | 601-006-00-1 |
Pentan-3-one | 606-006-00-5 |
Propan-1-ol | 603-003-00-0 |
Propyl acetate | 607-024-00-6 |
Propyl formate | 607-016-00-2 |
Propyl propionate | 607-030-00-9 |
Sodium bisulphite = polysulphite | 016-010-00-3 |
Toluene-2,4-diisocyanate | 615-006-00-4 |
Toluene-2,6-diisocyanate | 615-006-00-4 |
Cadmiumfluoride | 048-006-00-2 |
1,2-Epoxy-3(tolyloxy)-propane | 603-056-00-X |
Diphenylmethane-2,2′-diisocyanate | 615-005-00-9 |
Diphenylmethane-2,4′-diisocyanate | 615-005-00-9 |
Diphenylmethane-4,4′-diisocyanate | 615-005-00-9 |
Hydroquinone | 604-005-00-4 |
Hydroxypropyl acrylate | 607-108-00-2 |
Turpentine | 650-002-00-6 |
Butyl methyl ketone (2-Hexanone) | 606-030-00-6 |
Hexane | 601-007-00-7 |
Vanadium pentoxide | 023-001-00-8 |
Sodium nitrate | |
Zinc oxide |
This Directive | 88/379/EEC |
---|---|
Article 1 | Article 1 |
1.1 | 1.1 |
1.2 | 1.2 |
1.3 | |
1.4 | |
1.5 | 1.3 |
Article 2 | Article 2 |
Article 3 | Article 3.6 |
Article 4 | Article 3.1 |
Article 4 | |
Article 5 | Article 3.2 |
5.1 | 3.2 |
5.1, third indent | 3.2, paragraph 3(b) |
5.2—5.3 | |
5.4 | |
Article 6 | Article 3.3 |
6.1 | 3.3, paragraphs (a) and (b) |
6.2 | |
6.3 | 3.3, paragraphs 3 and 4 |
6.4 | 3.4 |
6.5 | 3.5, paragraphs 1 to 3 |
Article 7 | |
Article 8 | Article 5 |
8.1 | 5.1 |
8.2 | 5.2 |
8.3 | 5.3 |
8.4 | |
Article 9 | Article 6 |
9.1 | 6.1(a) |
9.2 | 6.1(b) |
9.3 | 6.2 and 6.3, second paragraph |
Article 10 | Article 7 |
10.1.1—1.2 | |
10.2 | 7.1 |
10.2.3. | 7.1(c) |
10.2.4. | 7.1(d) |
10.2.5. | 7.4 |
Article 11 | Article 8 |
Article 12 | Article 9 |
Article 13 | |
Article 14 | Article 10 |
Article 15 | Article 7 |
Article 16 | Article 11 |
Article 17 | Article 12 |
Article 18 | Article 13 |
Article 19 | Article 14 |
Article 20 | Article 15 |
Article 21 | |
Article 22 | Article 16 |
Article 23 | Article 16(3) |
Article 24 | Article 17 |
This Directive | 88/379/EEC | 90/35/EEC | 91/442/EEC | 93/18/EEC |
---|---|---|---|---|
Annex I.A | Article 3.2(2) | |||
Annex I.B | ||||
Annex II.A. introduction (1—3) | Annex I introduction | |||
Annex II.A. introduction (4) | ||||
Annex II.A.1 | Article 3.5(a) | |||
Annex II.A.1.1.1 | Article 3.5(a)(i) | |||
Annex II.A.1.1.2 | Article 3.5(a)(ii) | |||
Annex II.A.1.2 | Article 3.5(a)(iii) | |||
Annex II.A.2 | Article 3.5(b) | |||
Annex II.A.2.1.1 | Article 3.5(b)(i) | |||
Annex II.A.2.1.2 | Article 3.5(b)(ii) | |||
Annex II.A.2.2 | Article 3.5(b)(iii) | |||
Annex II.A.2.3 | Article 3.5(b)(iv) | |||
Annex II.A.3 | Article 3.5(c) | |||
Annex II.A.3.1.1 | Article 3.5(c)(i) | |||
Annex II.A.3.1.2 | Article 3.5(c)(ii) | |||
Annex II.A.3.2 | Article 3.5(c)(iii) | |||
Annex II.A.3.3 | Article 3.5(c)(iv) | |||
Annex II.A.4 | Article 3.5(d) | |||
Annex II.A.4.1.1 | Article 3.5(d)(i) | |||
Annex II.A.4.1.2 | Article 3.5(d)(ii) | |||
Annex II.A.4.2.1 | Article 3.5(e)(i) | |||
Annex II.A.4.2.2 | Article 3.5(e)(ii) | |||
Annex II.A.5 | Article 3.5(f) | |||
Annex II.A.5.1.1 | Article 3.5(f)(i) | |||
Annex II.A.5.1.2 | Article 3.5(f)(ii) | |||
Annex II.A.5.2.1 | Article 3.5(h)(i) | |||
Annex II.A.5.2.2 | Article 3.5(h)(ii) | |||
Annex II.A.5.3.1 | Article 3.5(g)(i) | |||
Annex II.A.5.3.2 | Article 3.5(g)(ii) | |||
Annex II.A.5.4.1 | Article 3.5(i)(i) | |||
Annex II.A.5.4.2 | Article 3.5(i)(ii) | |||
Annex II.A.6 | ||||
Annex II.A.6.1 | Article 3.5(g)(iii) | |||
Annex II.A.6.2 | Article 3.5(c)(v) | |||
Annex II.A.7.1 | Article 3.5(j) | Annex I.6 | ||
Annex II.A.7.2 | Article 3.5(k) | |||
Annex II.A.8.1 | Article 3.5(l), (m) | |||
Annex II.A.8.2 | Article 3.5(n) Article 3.5(o), (p) | |||
Annex II.A.9.1—9.4 | ||||
Annex II.B. introduction | Annex I. introduction | |||
Annex II.B.1 | Annex I.1 | |||
Annex II.B.1.1 | Annex I.1.1 | |||
Annex II.B.1.2 | Annex I.1.2 | |||
Annex II.B.2 | Annex I.2 | |||
Annex II.B.2.1 | Annex I.2.1 | |||
Annex II.B.2.2 | Annex I.2.2 | |||
Annex II.B.3 | Annex I.3 | |||
Annex II.B.3.1 | Annex I.3.1 | |||
Annex II.B.3.2 | Annex I.3.2 | |||
Annex II.B.4 | Annex I.4 | |||
Annex II.B.4.1 | Annex I.4.1 | |||
Annex II.B.4.2 | Annex I.4.2 | |||
Annex II.B.5 | Annex I.5 | |||
Annex II.B.5.1 | Annex I.5.1 | |||
Annex II.B.5.2 | Annex I.5.2 | |||
Annex II.B.6 | Annex I.6 | |||
Annex II.B.6.1 | Annex I.6.1 | |||
Annex II.B.6.2 | Annex I.6.2 | |||
Annex III.A | ||||
Annex III.B | ||||
Annex III.C | ||||
Annex IV.B | Articles 1 and 2 | |||
Annex IV.A.1 | Article 1(1) | |||
Annex IV.A.2 | Article 2; Annex (a) | |||
Annex IV.A.3 | Article 1; Annex (b) | |||
Annex V.A.1 | Annex II.A.1 | |||
Annex V.A.2 | Annex II.A.2 | |||
Annex V.A.3 | Annex II.A.3 | |||
Annex V.A.4 | Annex II.A.4 | |||
Annex V.B.1 | Annex II.B.1 | |||
Annex V.B.2 | Annex II.B.2 | |||
Annex V.B.3 | Annex II.B.3 | |||
Annex V.B.4 | Annex II.B.4 | |||
Annex V.B.5 | Annex II.B.5 | |||
Annex V.B.6 | Annex II.B.6 | |||
Annex V.B.7 | Article 3.2(3)(b) | |||
Annex V.B.8 | Article 3.5(4) | |||
Annex V.C | ||||
Annex VI | ||||
Annex VII | ||||
Annex VIII | ||||
Annex IX |
The Whole Directive you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Rhestrau you have selected contains over 200 provisions and might take some time to download. You may also experience some issues with your browser, such as an alert box that a script is taking a long time to run.
Would you like to continue?
Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.
Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE): Mae'r wreiddiol version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.
Pwynt Penodol mewn Amser: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.
Rhychwant ddaearyddol: Indicates the geographical area that this provision applies to. For further information see ‘Frequently Asked Questions’.
Dangos Llinell Amser Newidiadau: See how this legislation has or could change over time. Turning this feature on will show extra navigation options to go to these specific points in time. Return to the latest available version by using the controls above in the What Version box.
Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:
Mae’r llinell amser yma yn dangos y fersiynau gwahanol a gymerwyd o EUR-Lex yn ogystal ag unrhyw fersiynau dilynol a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig.
Cymerir dyddiadau fersiynau’r UE o ddyddiadau’r dogfennau ar EUR-Lex ac efallai na fyddant yn cyfateb â’r adeg pan ddaeth y newidiadau i rym ar gyfer y ddogfen.
Ar gyfer unrhyw fersiynau a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig, bydd y dyddiad yn cyd-fynd â’r dyddiad cynharaf y daeth y newid (e.e. ychwanegiad, diddymiad neu gyfnewidiad) a weithredwyd i rym. Am ragor o wybodaeth gweler ein canllaw i ddeddfwriaeth ddiwygiedig ar Ddeall Deddfwriaeth.
Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:
liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys