1.—(1) These Regulations may be cited as the Food for Particular Nutritional Uses (Addition of Substances for Specific Nutritional Purposes) (England) Regulations 2002 and extend to England only.
(2) Regulations 1, 5 and 10, and regulations 2 and 6 to 9 in so far as they relate to regulation 5, come into force on 5th August 2002.
(3) The remainder of these Regulations comes into force—
(a)on 5th August 2002 in relation to an L-tryptophan food; and
(b)in any other case on 1st April 2004.
2.—(1) In these Regulations—
“the Act” means the Food Safety Act 1990;
“designated PNU food” means any PNU food other than infant formulae, follow-on formulae, processed cereal-based foods and baby foods intended for infants and young children;
“Directive 89/398” means Council Directive 89/398/EEC M1 on the approximation of the laws of the Member States relating to foodstuffs intended for particular nutritional uses, as amended by Directive 1999/41/EC of the European Parliament and of the Council M2;
“Directive 2001/15” means Commission Directive 2001/15/EC M3 (as corrected M4) on substances that may be added for specific nutritional purposes in foods for particular nutritional uses [F1, as amended by Commission Directive 2004/5/EC [F2and Commission Directive 2006/34/EC] and as read with Commission Directive 2004/6/EC derogating from Directive 2001/15/EC to postpone the application of the prohibition of trade to certain products];
“food authority” does not include—
the council of a district of a non-metropolitan county except where the county functions have been transferred to that council pursuant to a structural change, or
the appropriate Treasurer referred to in section 5(1)(c) of the Act (which deals with the Inner Temple and the Middle Temple);
“L-tryptophan food” means any designated PNU food being a food to which L-tryptophan, or any of its sodium, potassium, calcium or magnesium salts or its hydrochloride, has been added for a specific nutritional purpose;
“PNU food” means a food for a particular nutritional use which—
owing to its special composition or process of manufacture, is clearly distinguishable from food intended for normal consumption, and
is sold in such a way as to indicate its suitability for its claimed particular nutritional purpose;
“particular nutritional use” means the fulfilment of the particular nutritional requirements of—
certain categories of persons whose digestive processes are, or whose metabolism is, disturbed, or
certain categories of person whose physiological condition renders them able to obtain a special benefit from the controlled consumption of any substance in food, or
infants or young children in good health; and
“sell” includes possess for sale and offer, expose or advertise for sale.
(2) Other expressions used both in these Regulations and in Directive 89/398 or 2001/15 have the same meaning in these Regulations as they have in the Directive concerned.
Textual Amendments
F1Words in reg. 2(1) inserted (31.3.2004) by The Food for Particular Nutritional Uses (Addition of Substances for Specific Nutritional Purposes) (England) (Amendment) Regulations 2004 (S.I. 2004/649), regs. 1(2), 3
F2Words in reg. 2(1) inserted (31.12.2006) by The Food for Particular Nutritional Uses (Addition of Substances for Specific Nutritional Purposes) (England) (Amendment) Regulations 2006 (S.I. 2006/3116), regs. 1(2), 3
Marginal Citations
M1OJ No. L186, 30.6.89, p.27.
M2OJ No. L172, 8.7.1999, p.38.
M3OJ No. L52, 22.2.2001, p.19.
M4OJ No. L253, 21.9.2001, p.34.
3.—[F3(1) Subject to paragraph (5), no person shall sell any designated PNU food being a food to which a substance falling within one of the categories mentioned in paragraph (2) has been added for a specific nutritional purpose unless —
(a)that substance is listed under that category —
(i)in the case of any food for special medical purposes, in Schedule 1 or 2; and
(ii)in any other case, in Schedule 1;
(b)that substance complies with the relevant purity criteria referred to in paragraph (3); and
(c)in the case of a substance listed in Schedule 2, the conditions of use (if any) set out in that Schedule relating to that substance are met.]
(2) For the purposes of paragraph (1), the categories are—
(a)vitamins,
(b)minerals,
(c)amino acids,
(d)carnitine and taurine,
(e)nucleotides, and
(f)choline and inositol.
(3) The relevant purity criteria for the purposes of paragraph (1)(b) are—
(a)the purity criteria, if any, specified by Community legislation for the use of the substance in question in the manufacture of food for purposes other than those covered by Directive 2001/15, or
(b)in the absence of such purity criteria, generally acceptable purity criteria for the substance in question recommended by international bodies.
(4) No person shall sell any designated PNU food in the manufacture of which any substance has been used for a specific nutritional purpose unless that food—
(a)is safe when used in accordance with the manufacturer’s instructions (if any); and
(b)fulfils the particular nutritional requirements of the persons for whom it is intended,
as established by generally accepted scientific data.
[F4(5) The restrictions in paragraph (1) shall not apply until 1st January 2007 in the case of a substance falling within one of the categories mentioned in paragraph (2) and listed under that category in Schedule 3 if —
(a)the European Food Safety Authority has not given an unfavourable opinion in respect of the use of that substance in the manufacture of any designated PNU food; and
(b)that substance was used in the manufacture of a food for a particular nutritional use which was on sale in the European Community on 11th February 2004.]
Textual Amendments
4. The manufacturer or, as the case may be, the importer of a designated PNU food in the manufacture of which a substance has been used for a specific nutritional purpose shall supply to the Food Standards Agency on request—
(a)a copy of the scientific work and data establishing that the use of that substance in the manufacture of that food results in a food which meets the criteria in regulation 3(4), or
(b)if such work and data are contained in a publication which is readily available, a reference to that publication.
5.—(1) Subject to paragraph (2), the manufacturer or, where appropriate, the importer of any notifiable food shall not sell any such food unless at least 3 months before placing food of that particular type on the market in England for the first time he notified the Food Standards Agency in writing by forwarding to it a model of the label to be used for that food and details of the composition of the food.
(2) Paragraph (1) shall not apply if the manufacturer or, where appropriate, the importer has already notified the Food Standards Agency before placing food of that particular type on the market elsewhere in the United Kingdom for the first time in accordance with an equivalent provision having effect there.
(3) In this regulation “notifiable food” means any L-tryptophan food which is—
(a)intended for use in energy-restricted diets for weight reduction;
(b)intended to meet the expenditure of intense muscular effort, especially for sportsmen; or
(c)for persons suffering from carbohydrate-metabolism disorders (diabetes).
6. Each food authority shall enforce and execute these Regulations in its area.
7. If any person—
(a)contravenes regulation 3(1) or (4), or
(b)without reasonable excuse contravenes regulation 4 or 5(1),
he shall be guilty of an offence and liable on summary conviction to a fine not exceeding level 5 on the standard scale.
F58. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Textual Amendments
F5Reg. 8 revoked (1.1.2006) by The Official Feed and Food Controls (England) Regulations 2005 (S.I. 2005/2626), reg. 1(b), Sch. 6 Pt. 2
9. The following provisions of the Act shall apply for the purposes of these Regulations with the modification that any reference in those provisions to the Act or Part thereof shall be construed as a reference to these Regulations—
(a)section 2 (extended meaning of “sale” etc.);
(b)section 3 (presumptions that food is intended for human consumption);
(c)section 20 (offences due to fault of another person);
(d)section 21 (defence of due diligence) as it applies for the purposes of section 8, 14 or 15;
(e)section 22 (defence of publication in the course of business);
(f)section 30(8) (which relates to documentary evidence);
(g)section 33(1) (obstruction etc. of officers);
(h)section 33(2), with the modification that the reference to “any such requirement as is mentioned in subsection (1)(b) above” shall be deemed to be a reference to any such requirement as is mentioned in that subsection as applied by paragraph (g) above;
(i)section 35(1) (punishment of offences) in so far as it relates to offences under section 33(1) as applied by paragraph (g) above;
(j)section 35(2) and (3) in so far as it relates to offences under section 33(2) as applied by paragraph (h) above;
(k)section 36 (offences by bodies corporate); and
(l)section 44 (protection of officers acting in good faith).
F610. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Textual Amendments
F6Reg. 10 revoked (11.11.2005) by The Tryptophan in Food (England) Regulations 2005 (S.I. 2005/2630), regs. 1, 10(2)
Signed by authority of the Secretary of State for Health
Hazel Blears
Parliamentary Under Secretary of State,
Department of Health