- Latest available (Revised)
- Original (As made)
The Medicines (Labelling of Medicinal Products for Incorporation in Animal Feeding Stuffs and of Medicated Animal Feeding Stuffs) Regulations 1988
You are here:
- UK Statutory Instruments
- 1988 No. 1009
- Table of contents
What Version
More Resources
Status:
This is the original version (as it was originally made). This item of legislation is currently only available in its original format.
4.Labelling requirements for containers and packages of medicinal products and excepted medicated feeding stuffs
5.Labelling requirements for containers and packages of medicated feeding stuffs other than excepted medicated feeding stuffs
7.Special labelling requirements relating to medicinal products exempt from product licences and medicated feeding stuffs in which such products have been incorporated
8.Sale or supply of medicinal products or medicated feeding stuffs not enclosed in a container
1.The name of the medicinal product or excepted medicated feeding...
2.Any product licence number as allocated by the licensing authority...
3.A statement, in a conspicuous position, of the quantity (expressed...
4.Where under paragraph 1 or 3 above a medicinal product,...
5.Where under paragraph 1 or 3 above a medicinal product,...
6.A description of the pharmaceutical form of the medicinal product...
7.The purposes for which the medicinal product or excepted medicated...
8.In the case of a medicinal product or excepted medicated...
9.The quantity of the medicinal product or excepted medicated feeding...
10.(a) Contra-indications, warnings and precautions required to be given by...
11.(a) Where a product licence relating to the medicinal product...
14.Either the expiry date of the medicinal product or excepted...
15.The manufacturer’s reference number of the batch to which the...
16.Any other statements or particulars required to be stated on...
17.In any case where particulars from this Schedule are omitted...
1.The name of the medicated feeding stuff, or a description...
2.(a) The name of any medicinal product or excepted medicated...
3.The appropriate non-proprietary name and quantity (expressed as mg per...
4.The medicinal purpose for which any medicinal product or excepted...
5.Directions for use, including— (a) instructions for the rate at...
6.(a) Any warnings or instructions relating to safety, storage or...
7.(a) Where the medicated feeding stuff contains a medicinal product...
8.The name and address of the manufacturer of the medicated...
9.If the period during which any active ingredient in the...
10.The manufacturer’s reference number of the batch to which the...
11.Any other statements or particulars required to be stated on...
12.In any case where particulars from this Schedule are omitted...
1.Such designation as will sufficiently identify the animal test.
2.(a) Where more than one medicinal product or excepted medicated...
3.The quantity of the medicinal product or of each active...
4.The purposes for which the medicinal product or medicated feeding...
5.In the case of a medicinal product or intermediate medicated...
6.Any special requirements for the handling and storage of the...
8.Any other statement or particulars required to be stated on...
9.In any case where particulars from this Schedule are omitted...
Options/Help
Print Options
PrintTable of Contents
PrintThe Whole Instrument
Legislation is available in different versions:
Latest Available (revised):The latest available updated version of the legislation incorporating changes made by subsequent legislation and applied by our editorial team. Changes we have not yet applied to the text, can be found in the ‘Changes to Legislation’ area.
Original (As Enacted or Made): The original version of the legislation as it stood when it was enacted or made. No changes have been applied to the text.
Opening Options
Different options to open legislation in order to view more content on screen at once
More Resources
Access essential accompanying documents and information for this legislation item from this tab. Dependent on the legislation item being viewed this may include:
- the original print PDF of the as enacted version that was used for the print copy
- lists of changes made by and/or affecting this legislation item
- confers power and blanket amendment details
- all formats of all associated documents
- correction slips
- links to related legislation and further information resources
More Resources
Use this menu to access essential accompanying documents and information for this legislation item. Dependent on the legislation item being viewed this may include:
- the original print PDF of the as made version that was used for the print copy
- correction slips
Click 'View More' or select 'More Resources' tab for additional information including:
- lists of changes made by and/or affecting this legislation item
- confers power and blanket amendment details
- all formats of all associated documents
- links to related legislation and further information resources
All content is available under the Open Government Licence v3.0 except where otherwise stated. This site additionally contains content derived from EUR-Lex, reused under the terms of the Commission Decision 2011/833/EU on the reuse of documents from the EU institutions. For more information see the EUR-Lex public statement on re-use.