Statutory Instruments
1995 No. 77
FOOD
The Infant Formula and Follow–on Formula Regulations 1995
Made
15th January 1995
Laid before Parliament
16th January 1995
Coming into force
1st March 1995
The Minister of Agriculture, Fisheries and Food, the Secretary of State for Health and the Secretary of State for Wales, acting jointly, in relation to England and Wales, and the Secretary of State for Scotland in relation to Scotland, in exercise of the powers conferred on them by sections 6(4), 16(1)(a), (b), (e) and (f), 17(1), 26(1) and (3) and 48(1) of the Food Safety Act 1990(1), and of all other powers enabling them in that behalf, and, in respect of regulation 21 of the following Regulations, the Secretary of State (being the Minister designated(2) for the purposes of section 2(2) of the European Communities Act 1972(3) in relation to informational and educational materials dealing with the feeding of infants and young children, donations of informational or educational equipment or materials, and donations and low price sales of supplies of infant formulae), in exercise of the powers conferred on him by the said section 2(2), and of all other powers enabling him in that behalf, after consultation in accordance with section 48 of the said Act of 1990 with such organisations as appear to them to be representative of interests likely to be substantially affected by the Regulations (in so far as the Regulations are made in exercise of the powers conferred by the said sections of the said Act of 1990), hereby make the following Regulations:—
Title, commencement and interpretation
1.—(1) These Regulations may be cited as the Infant Formula and Follow–on Formula Regulations 1995 and shall come into force on 1st March 1995.
(2) In these Regulations, unless the context otherwise requires—
“the Act” means the Food Safety Act 1990;
“advertisement” has the same meaning as in the Act, except that it does not include any label or wrapper, and “advertise” and “advertising” shall be construed accordingly;
“follow-on formula” means a food intended for particular nutritional use by infants in good health who are aged over four months, and constituting the principal liquid element in a progressively diversified diet;
“food authority” has the same meaning as in the Act, except that it does not include either the council of any district in a non–metropolitan county in England and Wales or the appropriate Treasurer referred to in section 5(1)(c) of the Act (which deals with the Inner Temple and the Middle Temple);
“health care system” means institutions or organisations engaged, directly or indirectly, in health care for mothers, infants and pregnant women, including nurseries or child–care institutions and health workers in private practice;
“infant” means a child under the age of twelve months;
“infant formula” means a food intended for particular nutritional use by infants in good health during the first four to six months of life, and satisfying by itself the nutritional requirements of such infants;
“member State” means a member State of the European Community other than the United Kingdom;
“presentation”, in relation to an infant formula or a follow-on formula, includes the shape, appearance or packaging of the product concerned, the way in which the product is arranged when it is exposed for sale and the setting in which the product is displayed with a view to sale, but does not include any form of labelling or advertising;
“sell” includes possess for sale and offer, expose or advertise for sale, but does not include—
(a)
an advertisement of the type described in section 22 of the Act (publication in the course of business), or
(b)
anything not qualifying as a placing on the market for the purposes of Council Directive 89/398/EEC(4) on the approximation of the laws of the Member States relating to foodstuffs intended for particular nutritional uses;
“third country” means a country or territory other than a member State, the United Kingdom, the Isle of Man or any of the Channel Islands;
“young children” means children aged between one and three years.
(3) Any reference in these Regulations to a numbered regulation or Schedule shall be construed as a reference to the regulation or Schedule bearing that number in these Regulations.
Conditions for the sale of infant formulae and follow-on formulae
2. No person shall sell any food which is labelled or otherwise represented as—
(a)being an infant formula; or
(b)satisfying by itself the nutritional requirements of normal healthy infants during the first four to six months of life,
unless that food—
(i)has been manufactured in accordance with the requirements set out in regulations 8(1) and (2), 10 and 11;
(ii)complies with the compositional criteria referred to in regulation 8(3), and the compositional requirements of regulation 12;
(iii)is labelled in accordance with the requirements for an infant formula of regulations 13 and 15; and
(iv)complies with the requirements as to presentation referred to in regulation 16(1).
3. No person shall sell any food which is labelled or otherwise represented as being a follow-on formula unless that food—
(a)has been manufactured in accordance with the requirements set out in regulations 9(1) and (2), 10 and 11;
(b)complies with the compositional criteria referred to in regulation 9(3), and the compositional requirements of regulation 12;
(c)is labelled in accordance with the requirements for a follow-on formula of regulations 14 and 15; and
(d)complies with the requirements as to presentation referred to in regulation 16(2).
4. Nothing in regulation 2 or regulation 3 shall apply to a sale of any food solely intended for export to a third country.
Export of infant formulae and follow-on formulae to third countries
5.—(1) No person shall export from Great Britain to a third country any infant formula which does not comply with—
(a)the requirements referred to in regulations 8, 10, 11 and 12 or the Codex Standard for Infant Formula(5) established by the Codex Alimentarius;
(b)the requirements referred to in regulations 13(1)(c)–(h), (2) and (3), 15 and 16(1); and
(c)the provisions of the Food (Lot Marking) Regulations 1992(6).
(2) The provisions referred to in paragraph (1) above shall not apply to the extent that any of them are dispensed with or varied by provisions laid down by the importing country.
(3) No person shall export from Great Britain to a third country any food, other than an infant formula, which is labelled or otherwise represented as capable of satisfying by itself the nutritional requirements of normal healthy infants during the first four to six months of life.
6.—(1) No person shall export from Great Britain to a third country any follow-on formula which does not comply with—
(a)the requirements referred to in regulations 9, 10, 11 and 12 or the Codex Standard for Follow–up Formula(7) established by the Codex Alimentarius;
(b)the requirements referred to in regulations 14(c)–(f), 15 and 16(2); and
(c)the provisions of the Food (Lot Marking) Regulations 1992.
(2) The provisions referred to in paragraph (1) above shall not apply to the extent that any of them are dispensed with or varied by provisions laid down by the importing country.
7. No person shall export from Great Britain to a third country any infant formula or follow-on formula which is not—
(a)labelled in an appropriate language (or appropriate languages); and
(b)labelled in such a way as to avoid any risk of confusion between an infant formula and a follow-on formula.
Composition of infant formulae and follow-on formulae
8.—(1) An infant formula shall be manufactured only from—
(a)the protein sources and food ingredients specified in Schedule 1, and
(b)other food ingredients the suitability of which for particular nutritional use by infants from birth has been established by generally accepted scientific data.
(2) In the manufacture of any infant formula the prohibitions and limitations on the use of food ingredients set out in Schedule 1 shall be observed.
(3) The composition of an infant formula shall conform to the criteria specified in Schedule 1.
(4) In this regulation a reference to Schedule 1 shall be read as a reference to that Schedule as read with Schedules 5 and 6.
9.—(1) A follow-on formula shall be manufactured only from—
(a)the protein sources and food ingredients specified in Schedule 2, and
(b)other food ingredients the suitability of which for particular nutritional use by infants aged over four months has been established by generally accepted scientific data.
(2) In the manufacture of any follow-on formula the prohibitions and limitations on the use of food ingredients set out in Schedule 2 shall be observed.
(3) The composition of a follow-on formula shall conform to the criteria specified in Schedule 2.
(4) In this regulation a reference to Schedule 2 shall be read as a reference to that Schedule as read with Schedules 6 and 7.
10. If an infant formula or a follow-on formula is not at the time it is sold ready for use, nothing more than the addition of water shall be required to make it ready for such use.
11.—(1) Subject to paragraph (2) below, in relation to the manufacture of any infant formula or any follow-on formula, the requirements specified in Schedule 1 or Schedule 2, as appropriate, in respect of vitamins, mineral substances, amino acids and other nitrogen compounds, and other substances having a particular nutritional purpose shall only be satisfied by the use in the process of manufacture of the vitamin formulations, permitted salts, amino acids and other nitrogen compounds and other substances listed in Schedule 3.
(2) In the case of a vitamin or a mineral substance listed in column 1 of Schedule 3 the vitamin formulation or permitted salt to be used shall be one of those listed in column 2 of that Schedule in relation to the vitamin or mineral substance in question.
12. No infant formula or follow-on formula shall contain any substance in such quantity as to endanger the health of infants.
Labelling, packaging etc of infant formulae and follow-on formulae
13.—(1) No infant formula shall be sold unless it is labelled with the following particulars—
(a)in the case of a product where the protein source is not entirely cows' milk proteins, the name “infant formula”;
(b)in the case of a product where the protein source is entirely cows' milk proteins, the name “infant milk”;
(c)a statement to the effect that the product is suitable for particular nutritional use by infants from birth when they are not breast–fed;
(d)in the case of a product which does not contain added iron, a statement to the effect that the product does not contain the total iron requirements recommended for an infant over the age of four months, and that these should be made up from additional sources;
(e)the available energy value expressed in kJ and kcal, and the content of proteins, lipids and carbohydrates per 100 millilitres of the product ready for use;
(f)he average quantity of each mineral substance and of each vitamin mentioned in Schedule 1, and where applicable of choline, inositol and carnitine, per 100 millilitres of the product ready for use;
(g)instructions for appropriate preparation of the product and a warning against the health hazards of inappropriate preparation; and
(h)the words “Important Notice”, immediately followed by—
(i)a statement concerning the superiority of breast–feeding; and
(ii)a statement recommending that the product be used only on the advice of an independent person qualified in medicine, nutrition or pharmacy or having a professional qualification in maternal or child care.
(2) The labelling of an infant formula shall not include—
(a)any picture of an infant;
(b)any other picture or text which may idealise the use of the product,
but may include graphic representations for easy identification of the product or for illustrating methods of preparation.
(3) The labelling of an infant formula shall include a claim concerning the composition of the product only when—
(a)the claim is listed in column 1 of Schedule 4, and is expressed in the terms there set out; and
(b)the condition specified in column 2 of that Schedule in relation to the relevant claim made in column 1 is satisfied.
14. No follow-on formula shall be sold unless it is labelled with the following particulars—
(a)in the case of a product where the protein source is not entirely cows' milk proteins, the name “follow-on formula”;
(b)in the case of a product where the protein source is entirely cows' milk proteins, the name “follow-on milk”;
(c)a statement to the effect that the product is suitable only for particular nutritional use by infants over the age of four months, that it should form only part of a diversified diet and that it is not to be used as a substitute for breast milk during the first four months of life;
(d)the available energy value expressed in kJ and kcal, and the content of proteins, lipids and carbohydrates per 100 millilitres of the product ready for use;
(e)the average quantity of each mineral substance and of each vitamin mentioned in Schedule 2, and where applicable of choline, inositol and carnitine per 100 millilitres of the product ready for use; and
(f)nstructions for appropriate preparation of the product and a warning against the health hazards of inappropriate preparation.
15. The labelling of any infant formula and any follow-on formula shall—
(a)be designed to provide the necessary information about the appropriate use of the product so as not to discourage breast–feeding;
(b)not contain the terms “humanized”, “maternalized” or any similar term suggesting that the product is equivalent or superior to breast milk,
and the term “adapted” may be used only in relation to adapted protein and then only in conformity with the provisions of regulation 13(3).
16.—(1) The provisions of regulations 13(1)(h), (2) and (3) and 15 shall also apply so far as they are relevant to the presentation of an infant formula.
(2) The provisions of regulation 15 shall also apply so far as they are relevant to the presentation of a follow-on formula.
Restrictions on advertising of infant formulae
17.—(1) No person shall publish or display any advertisement for an infant formula—
(a)except—
(i)in a publication specialising in baby care and distributed only through the health care system;
(ii)in a scientific publication; or
(iii)for the purposes of trade prior to the retail stage, in a publication of which the intended readership is other than the general public; and
(b)which does not comply with the requirements, prohibitions and restrictions relating to labelling contained in regulations 13(1)(h), (2) and (3) and 15.
(2) An advertisement for an infant formula shall contain only information of a scientific and factual nature. Such information shall not imply or seek to create a belief that bottle–feeding is equivalent or superior to breast–feeding.
Restrictions on advertising of follow-on formulae
18. No person shall publish or display any advertisement for a follow-on formula which does not comply with the requirements, prohibitions and restrictions relating to labelling contained in regulation 15.
Restrictions on promotion of infant formulae
19. No person shall at any place where any infant formula is sold by retail—
(a)advertise any infant formula;
(b)make any special display of an infant formula designed to promote sales;
(c)give away—
(i)any infant formula as a free sample; or
(ii)any coupon which may be used to purchase an infant formula at a discount;
(d)promote the sale of an infant formula by means of premiums, special sales, loss– leaders or tie–in sales; or
(e)undertake any other promotional activity to induce the sale of an infant formula.
20. No manufacturer or distributor of any infant formula shall provide for promotional purposes any infant formula free or at a reduced or discounted price, or any gift designed to promote the sale of an infant formula, to—
(a)the general public;
(b)pregnant women;
(c)mothers; or
(d)members of the families of persons mentioned in sub–paragraphs (b) and (c) above,
either directly, or indirectly through the health care system or health workers.
Provision of information and education regarding infant and child feeding
21.—(1) No person shall produce or publish any informational and educational (or informational or educational) materials, whether written or audiovisual, dealing with the feeding of infants and intended to reach pregnant women and mothers of infants and young children, unless (subject to paragraph (2) below) such materials include clear information on all the following points—
(a)the benefits and superiority of breast–feeding;
(b)maternal nutrition and the preparation for, and the maintenance of, breast– feeding;
(c)the possible negative effect on breast–feeding of introducing partial bottle– feeding;
(d)the difficulty of reversing the decision not to breast–feed; and
(e)where needed, the proper use of an infant formula or of infant formulae, whether manufactured industrially or home prepared.
(2) When the materials referred to in paragraph (1) above contain information about the use of an infant formula, they—
(a)shall include the social and financial implications of its use; the health hazards of inappropriate foods or feeding methods, and, in particular, the health hazards of improper use of an infant formula, and
(b)shall not use any pictures which may idealise the use of infant formulae.
(3) No manufacturer or distributor of an infant formula shall make a donation of any informational or educational equipment or materials except in accordance with the following conditions—
(a)the donation shall be made following a request by the intended recipient;
(b)the donation shall be made with the written authority of the Secretary of State or in accordance with guidelines drawn up by the Secretary of State;
(c)the equipment and materials may bear the name or logo of the donor but shall not be marked or labelled with the name of a proprietary infant formula; and
(d)the equipment or materials shall be distributed only through the health care system.
(4) Any institution or organisation which receives any infant formula free or at a reduced price shall ensure that such infant formula is only used by or distributed for infants who have to be fed on infant formula, and that such use or distribution continues only so long as is required by such infants.
Offences and enforcement
22.—(1) If any person contravenes or fails to comply with any of the provisions contained in regulations 2, 3, 5, 6, 7, 17, 18, 19, 20 and 21 he shall be guilty of an offence and shall be liable on summary conviction to a fine not exceeding level 5 on the standard scale.
(2) Each food authority shall enforce and execute these Regulations in its area.
Application of provisions of the Food Safety Act 1990
23. The following provisions of the Act shall apply for the purposes of these Regulations (except regulation 21) as they apply for the purposes of section 8, 14 or 15 of the Act, and, unless the context otherwise requires, any reference in them to the Act shall be construed for the purposes of these Regulations as a reference to these Regulations (except regulation 21)—
(a)section 2 (extended meaning of “sale” etc.);
(b)section 3 (presumption that food is intended for human consumption);
(c)section 20 (offences due to fault of another person);
(d)section 21 (defence of due diligence);
(e)section 30(8) (which relates to documentary evidence);
(f)ection 33 (obstruction etc. of officers);
(g)section 36 (offences by bodies corporate);
(h)section 44 (protection of officers acting in good faith).
Amendments to existing Regulations
24. The Skimmed Milk with Non–Milk Fat Regulations 1960(8) and the Skimmed Milk with Non–Milk Fat (Scotland) Regulations 1960(9) shall be amended in each case as follows—
(a)at the end of regulation 2(3) there shall be added the following words—
“or any infant formula which complies with the requirements as to its manufacture and composition specified in regulations 9(1), (2) and (3), 10, 11 and 12 of the Infant Formula and Follow–on Formula Regulations 1995.”; and
(b)the following deletions shall be made—
(i)in regulation 3(1)(a), the words “(as modified by the Second Schedule to these Regulations in respect of the specified foods referred to therein)”;
(ii)in Part I of Schedule 1, sub–paragraph (j) of the Proviso in paragraph 1;
(iii)Schedule 2.
25. The Food Labelling Regulations 1984(10) and the Food Labelling (Scotland) Regulations 1984(11) shall be amended by the deletion in each case of paragraph 2 in Part I of Schedule 6.
Angela Browning
Parliamentary Secretary, Ministry of Agriculture, Fisheries and Food
3rd January 1995
Signed by authority of the Secretary of State for Health:
Cumberlege
Parliamentary Under Secretary of State,
Department of Health
28th December 1994
John Redwood
Secretary of State, Welsh Office
15th January 1995
Fraser of Carmyllie
Minister of State, Scottish Office
30th December 1994
Regulations 8, 11 and 13(1)(f)
SCHEDULE 1ESSENTIAL COMPOSITION OF INFANT FORMULAE WHEN RECONSTITUTED AS INSTRUCTED BY THE MANUFACTURER(All values refer to the product ready for use)
Energy
Minimum
Maximum
250 kJ
315 kJ
(60 kcal/100 ml)
(75 kcal/100 ml)
Proteins
2. (Protein content=nitrogen content × 6.38) for cows' milk proteins.
(Protein content=nitrogen content × 6.25) for soya protein isolates.
(2.1) Formulae manufactured from unmodified cows' milk proteins
Minimum
Maximum
The chemical index of the proteins present shall be equal to at least 80% of that of the reference protein (breast milk, as defined in Schedule 6); nevertheless, for calculation purposes, the concentrations of methionine and cystine may be added together.
The “chemical index” shall mean the lowest of the ratios between the quantity of each essential amino acid of the test protein and the quantity of each corresponding amino acid of the reference protein.
0.56 g/100 kJ
0.7 g/100 kJ
(2.25 g/100 kcal)
(3 g/100 kcal)
(2.2) Formulae manufactured from modified cows' milk proteins (alteration of the casein/ whey protein ratio)
Minimum
Maximum
For an equal energy value, the formula must contain an available quantity of each essential and semi–essential amino acid at least equal to that contained in the reference protein (breast milk, as defined in Schedule 5).
0.45 g/100 kJ
0.7 g/100 kJ
(1.8 g/100 kcal)
(3 g/100 kcal)
(2.3) Formulae manufactured from soya protein isolates, alone or in a mixture with cows' milk proteins
Minimum
Maximum
Only soya protein isolates may be used in manufacturing these formulae.
The chemical index shall be equal to at least 80% of that of the reference protein (breast milk, as defined in Schedule 6).
For an equal energy value the formula must contain an available quantity of methionine at least equal to that contained in the reference protein (breast milk, as defined in Schedule 5).
The L–carnitine content shall be at least equal to 1.8 μmoles/100 kJ (7.5 μmoles/100 kcal).
0.56 g/100 kJ
0.7 g/100 kJ
(2.25 g/100 kcal)
(3 g/100 kcal)
(2.4) In all cases,the addition of amino acids is permitted solely for the purpose of improving the nutritional value of the proteins, and only in the proportions necessary for that purpose.
Lipids
Minimum
Maximum
0.8 g/100 kJ
1.5 g/100 kJ
(3.3 g/100 kcal)
(6.5 g/100 kcal)
(3.1) The use of the following substances is prohibited:
sesame seed oil;
cotton seed oil;
fats containing more than 8% trans isomers of fatty acids.
(3.2) Lauric acid
Minimum
Maximum
—
15% of the total fat content
(3.3) Myristic acid
Minimum
Maximum
—
15% of the total fat content
(3.4) Linoleic acid (in the form of glycerides=linoleates)
Minimum
Maximum
70 mg/100 kJ
285 mg/100 kJ
(300 mg/100 kcal)
1200 mg/100 kcal)
Carbohydrates
Minimum
Maximum
1.7 g/100 kJ
3.4 g/100 kJ
(7 g/100 kcal)
(14 g/100 kcal)
(4.1) Only the following carbohydrates may be used:
lactose;
maltose;
sucrose;
malto–dextrins;
glucose syrup or dried glucose syrup;
pre–cooked starch ) naturally free
gelatinised starch ) of gluten
(4.2) Lactose
Minimum
Maximum
This provision does not apply to formulae in which soya proteins represent more than 50% of the total protein content.
0.85 g/100 kJ
—
(3.5 g/100 kcal)
—
(4.3) Sucrose
Minimum
Maximum
—
20% of the total carbohydrate content
(4.4) Pre–cooked starch and/or gelatinised starch
Minimum
Maximum
—
2 g/100 ml, and 30% of the total carbohydrate content
Mineral substances
5.—(5.1) Formulae manufactured from cows' milk proteins
per 100 kJ
per 100 kcal
Minimum
Maximum
Minimum
Maximum
The calcium/phosphorus ratio shall not be less than 1.2 nor greater than 2.0.
Sodium
(mg)
5
14
20
60
Potassium
(mg)
15
35
60
145
Chloride
(mg)
12
29
50
125
Calcium
(mg)
12
—
50
—
Phosphorus
(mg)
6
22
25
90
Magnesium
(mg)
1.2
3.6
5
15
Iron
(mg)(12)
0.12
0.36
0.5
1.5
Zinc
(mg)
0.12
0.36
0.5
1.5
Copper
(μg)
4.8
19
20
80
Iodine
(μg)
1.2
—
5
—
(5.2) Formulae manufactured from soya proteins, alone or in a mixture with cows' milk proteins
All requirements of paragraph 5.1. are applicable except those concerning iron and zinc, which are as follows:
per 100 kJ
per 100 kcal
Minimum
Maximum
Minimum
Maximum
Iron
(mg)
0.25
0.5
1
2
Zinc
(mg)
0.18
0.6
0.75
2.4
Vitamins
per 100 kJ
per 100 kcal
Minimum
Maximum
Minimum
Maximum
Vitamin A
(μg–RE)(13)
14
43
60
180
Vitamin D
(μg)(14)
0.25
0.65
1
2.5
Thiamin
(μg)
10
—
40
—
Riboflavin
(μg)
14
—
60
—
Nicotinamide
(μg–NE)(15)
60
—
250
—
Pantothenic
acid
(μg)
70
—
300
—
Vitamin B6
(μg)
9
—
35
—
Biotin
(μg)
0.4
—
1.5
—
Folic acid
(μg)
1
—
4
—
VitaminB12
(μg)
0.025
—
0.1
—
Vitamin C
(mg)
1.9
—
8
—
Vitamin K
(μg)
1
—
4
—
Vitamin E
(mg*–TE)(16)
0.5/g of
—
0.5/g of
—
polyunsaturated fatty acids expressed as linoleic acid but in no case less than 0.1 mg per 100 available kJ
polyunsaturated fatty acids expressed as linoleic acid but in no case less than 0.5 mg per 100 available kcal
Regulations 9, 11 and 14(e)
SCHEDULE 2ESSENTIAL COMPOSITION OF FOLLOW–ON FORMULAE WHEN RECONSTITUTED AS INSTRUCTED BY THE MANUFACTURER(All values refer to the product ready for use)
Energy
Minimum
Maximum
250 kJ/100 ml
335 kJ/100 ml
(60 kcal/100 ml)
(80 kcal/100 ml)
Proteins
2. (Protein content–nitrogen content × 6.38) for cows' milk proteins.
(Protein content–nitrogen content × 6.25) for soya protein isolates.
Minimum
Maximum
The chemical index of the proteins present shall be at least equal to 80% of that of the reference protein (casein as defined in Schedule 6).
The “chemical index” shall mean the lowest of the ratios between the quantity of each essential amino acid of the test protein and the quantity of each corresponding amino acid of the reference protein.
For follow-on formulae manufactured from soya proteins, alone or in a mixture with cows' milk proteins, only protein isolates from soya may be used.
Amino acids may be added to follow-on formulae for the purpose of improving the nutritional value of the proteins, in the proportions necessary for that purpose.
0.5 g/100 kJ
1 g/100 kJ
(2.25 g/100 kcal)
(4.5 g/100 kcal)
Lipids
Minimum
Maximum
0.8 g/100 kJ
1.5 g/100 kJ
(3.3 g/100 kcal)
(6.5 g/100 kcal)
(3.1) The use of the following substances is prohibited:
sesame seed oil;
cotton seed oil;
fats containing more than 8% trans isomers of fatty acids.
(3.2) Lauric acid
Minimum
Maximum
—
15% of the total fat content
(3.3) Myristic acid
Minimum
Maximum
—
15% of the total fat content
(3.4) Linoleic acid (in the form of glycerides=linoleates)
Minimum
Maximum
70 mg/100 kJ (300 mg/100 kcal): this limit applies only to follow-on formulae containing vegetable oils
—
Carbohydrates
Minimum
Maximum
1.7 g/100 kJ
3.4 g/100 kJ
(7 g/100 kcal)
(14 g/100 kcal)
(4.1) The use of ingredients containing gluten is prohibited.
(4.2) Lactose
Minimum
Maximum
This provision does not apply to follow-on formulae in which soya protein isolates represent more than 50% of the total protein content.
0.45 g/100 kJ
—
(1.8 g/100 kcal)
—
(4.3) Sucrose, fructose, honey
Minimum
Maximum
—
separately or as a whole: 20% of the total carbohydrate content
Mineral substances
per 100 kJ
per 100 kcal
Minimum
Maximum
Minimum
Maximum
Iron
(mg)
0.25
0.5
1
2
Iodine
(μg)
1.2
—
5
—
(5.2) Zinc
(5.2.1)Follow–on formulae manufactured entirely from cows' milk proteins
Minimum
Maximum
0.12 mg/100 kJ
—
(0.5mg/100 kcal)
—
(5.2.2)Follow–on formulae containing soya protein isolates, alone or mixed with cows' milk proteins
Minimum
Maximum
0.18 mg/100 kJ
—
(0.75mg/100 kcal)
—
(5.3) Other mineral substances:
The concentrations are at least equal to those normally found in cows' milk, reduced, where appropriate, in the same ratio as the protein concentration of the follow-on formulae to that of cows' milk. The typical composition of cows' milk is given, for guidance, in Schedule 7.
(5.4) The calcium/phosphorus ratio shall not exceed 2.0.
Vitamins
per 100 kJ
per 100 kcal
Minimum
Maximum
Minimum
Maximum
Vitamin A
(μg–RE)(17)
14
43
60
180
Vitamin D
(μg)(18)
0.25
0.75
1
3
Vitamin C
(mg)
1.9
—
8
—
Vitamin E
(mg*–TE)(19)
0.5/g of
—
0.5/g of
—
polyunsaturated fatty acids expressed as linoleic acid but in no case less than 0.1 mg per 100 available kJ
polyunsaturated fatty acids expressed as linoleic acid but in no case less than 0.5 mg per 100 available kcal
Regulation 11
SCHEDULE 3NUTRITIONAL SUBSTANCES
Vitamins
Vitamin
Vitamin formulation
Vitamin A
Retinyl acetate
Retinyl palmitate
Beta–carotene
Retinol
Vitamin D
Vitamin D2 (ergocalciferol)
Vitamin D3 (cholecalciferol)
Vitamin B1
Thiamin hydrochloride
Thiamin mononitrate
Vitamin B2
Riboflavin
Riboflavin–5'–phosphate, sodium
Niacin
Nicotinamide
Nicotinic acid
Vitamin B6
Pyridoxine hydrochloride
Pyridoxine–5'–phosphate
Folate
Folic acid
Pantothenic acid
D–pantothenate, calcium
D–pantothenate, sodium
Dexpanthenol
Vitamin B12
Cyanocobalamin
Hydroxocobalamin
Biotin
D–Biotin
Vitamin C
L–ascorbic acid
Sodium L–ascorbate
Calcium L–ascorbate
6–palmityl–L–ascorbic acid (ascorbyl palmitate)
Potassium ascorbate
Vitamin E
D–alpha tocopherol
DL–alpha tocopherol
D–alpha tocopherol acetate
DL–alpha tocopherol acetate
Vitamin K
Phylloquinone (Phytomenadione)
Mineral substances
Mineral substances
Permitted salts
Calcium (Ca)
Calcium carbonate
Calcium chloride
Calcium salts of citric acid
Calcium gluconate
Calcium glycerophosphate
Calcium lactate
Calcium salts of orthophosphoric acid
Calcium hydroxide
Magnesium (Mg)
Magnesium carbonate
Magnesium chloride
Magnesium oxide
Magnesium salts of orthophosphoric acid
Magnesium sulphate
Magnesium gluconate
Magnesium hydroxide
Magnesium salts of citric acid
Iron (Fe)
Ferrous citrate
Ferrous gluconate
Ferrous lactate
Ferrous sulphate
Ferric ammonium citrate
Ferrous fumarate
Ferric diphosphate (Ferric pyrophosphate)
Copper (Cu)
Cupric citrate
Cupric gluconate
Cupric sulphate
Copper–lysine complex
Cupric carbonate
Iodine (I)
Potassium iodide
Sodium iodide
Potassium iodate
Zinc (Zn)
Zinc acetate
Zinc chloride
Zinc lactate
Zinc sulphate
Zinc citrate
Zinc gluconate
Zinc oxide
Manganese (Mn)
Manganese carbonate
Manganese chloride
Manganese citrate
Manganese sulphate
Manganese gluconate
Sodium (Na)
Sodium bicarbonate
Sodium chloride
Sodium citrate
Sodiu gluconate
Sodium carbonate
Sodium lactate
Sodium salts of orthophosphoric acid
Sodium hydroxide
Potassium (K)
Potassium bicarbonate
Potassium carbonate
Potassium chloride
Potassium salts of citric acid
Potassium gluconate
Potassium lactate
Potassium salts of orthophosphoric acid
Potassium hydroxide
Amino acids and other nitrogen compounds
3. L–arginine and its hydrochloride
L–cystine and its hydrochloride
L–histidine and its hydrochloride
L–isoleucine and its hydrochloride
L–leucine and its hydrochloride
L–lysine and its hydrochloride
L–cysteine and its hydrochloride
L–methionine
L–phenylalanine
L–threonine
L–tryptophan
L–tyrosine
L–valine
L–carnitine and its hydrochloride
Taurine
Others
4. Choline
Choline chloride
Choline citrate
Choline bitartrate
Inositol
Regulation 13(3)
SCHEDULE 4COMPOSITIONAL CRITERIA FOR INFANT FORMULAE, WARRANTING A CORRESPONDING CLAIM
Claim related to
Conditions warranting the claim
1. Adapted protein
The protein content is lower than 0.6 g/100 kJ (2.5 g/ 100 kcal) and the whey protein/casein ratio is not less than 1.0
2. Low sodium
The sodium content is lower than 9 mg/100 kJ (39 mg/100 kcal)
3. Sucrose free
No sucrose is present
4. Lactose only
Lactose is the only carbohydrate present
5. Lactose free
No lactose is present(20)
6. Iron enriched
Iron is added
Regulation 8
SCHEDULE 5THE ESSENTIAL AND SEMI–ESSENTIAL AMINO ACIDS IN BREAST MILK
For the purpose of these Regulations, the essential and semi–essential amino acids in breast milk, expressed in mg per 100 kJ and 100 kcal, are the following:
per 100 kJ(21)
per 100 kcal
Arginine
16
69
Cystine
6
24
Histidine
11
45
Isoleucine
17
72
Leucine
37
156
Lysine
29 122
Methionine
7
29
Phenylalanine
15
62
Threonine
19
80
Tryptophan
7
30
Tyrosine
14
59
Valine
19
80
Regulations 8 and 9
SCHEDULE 6AMINO ACID COMPOSITION OF CASEIN AND BREAST MILK PROTEIN
The amino acid composition of casein and breast milk protein (g/100 g of protein):
Casein(22)
Breast milk(22)
Arginine
3.7
3.8
Cystine
0.3
1.3
Histidine
2.9
2.5
Isoleucine
5.4
4.0
Leucine
9.5
8.5
Lysine
8.1
6.7
Methionine
2.8
1.6
Phenylalanine
5.2
3.4
Threonine
4.7
4.4
Tryptophan
1.6
1.7
Tyrosine
5.8
3.2
Valine
6.7
4.5
Regulation 9
SCHEDULE 7THE MINERAL ELEMENTS IN COWS' MILK
As a reference, the contents of mineral elements in cows' milk expressed per 100 g of solids–non–fat and per g of proteins are the following:
per 100 g SNF(23)
per g of proteins
Sodium (mg)
550
15
Potassium (mg)
1680
43
Chloride (mg)
1050
28
Calcium (mg)
1350
35
Phosphorus (mg)
1070
28
Magnesium (mg)
135
3.5
Copper (μg)
225
6
Iodine
NS(24)
NS
Explanatory Note
(This note is not part of the Regulations)
These Regulations, which apply to Great Britain, come into force on 1st March 1995.
They implement Commission Directive 91/321/EEC (OJ No. L175, 4.7.91, p.35) on infant formulae (which are foods suitable as the sole source of nutrition for infants during the first four to six months of life and often form an important part of the diet throughout infancy) and follow-on formulae (which are foods given to older infants and young children as an alternative to milk or infant formulae). They also implement Council Directive 92/52/EEC (OJ No. L179, 1.7.92, p.129) on infant formulae and follow-on formulae intended for export to third countries.
The principal provisions of the Regulations—
(1) prohibit the sale of food labelled as infant formulae or follow-on formulae unless it complies with the requirements of the Regulations as to composition, labelling, appearance and packaging (regulations 2, 3 and 8 to 16);
(2) require infant formulae and follow-on formulae exported to countries not in the European Community to comply with similar compositional standards unless the importing country otherwise permits and require products to be labelled in an appropriate language and in a way which avoids confusion between infant formulae and follow-on formulae (regulations 5, 6 and 7);
(3) limit the advertising of infant formulae to specified types of publications and restrict the content of advertisements for infant formulae and follow-on formulae (regulations 17 and 18);
(4) prohibit special displays or promotions of infant formulae at retail outlets (regulation 19);
(5) prohibit the promotion of infant formulae to the general public, expectant mothers, and others by providing such formulae free or at reduced prices (regulation 20);
(6) lay down requirements as to the information to be contained in informational and educational materials dealing with the feeding of infants and intended to reach pregnant women and mothers of infants and young children, and regulate the cases in which a manufacturer or distributor of infant formulae may make gifts of informational or educational equipment or materials (regulation 21).
The standards for infant formula or follow-on formula established by the Codex Alimentarius are available for inspection at the Library of the Ministry of Agriculture, Fisheries and Food, Whitehall Place, London SW1A 2HH and at the Scottish Office, New St. Andrew’s House, St. James' Square, Edinburgh EH1 3TE.
A Compliance Cost Assessment in relation to these Regulations has been placed in the libraries of both Houses of Parliament and copies can be obtained from the Consumer Protection Division of the Ministry of Agriculture, Fisheries and Food, Ergon House, 17 Smith Square, London SW1P 3JR.
(1)
1990 c. 16; “the Ministers” is defined in section 4(1) of the Act.
(2)
S.I. 1994/1887.
(3)
1972 c. 68.
(4)
OJ No. L186, 30.6.89, p.27.
(5)
Codex Stan 72–1981 (amended 1983, 1985, 1987), Codex Alimentarius, 1994, vol. 4, p. 17.
(6)
S.I. 1992/1357.
(7)
Codex Stan 156–1987 (amended 1989), Codex Alimentarius, 1994, vol. 4, p. 43.
(8)
S.I. 1960/2331; relevant amending instruments are S.I. 1976/103 and 1981/1174.
(9)
S.I. 1960/2437, amended by S.I. 1976/294 and 1981/1319.
(10)
S.I. 1984/1305, to which there are amendments not relevant to these Regulations.
(11)
S.I. 1984/1319, to which there are amendments not relevant to these Regulations.
(12)
Limit applicable to formulae with added iron.
(13)
RE=all trans retinol equivalent.
(14)
In the form of cholecalciferol, of which 10 μg=400 i.u. of vitamin D.
(15)
NE=Niacin equivalent=mg nicotinic acid+mg tryptophan/60.
(16)
*–TE=d–*–tocopherol equivalent.
(17)
RE=all trans retinol equivalent.
(18)
In the form of cholecalciferol, of which 10 μg=400 i.u. of vitamin D.
(19)
*–TE=d–*–tocopherol equivalent.
(20)
When determined by a method the detection limits of which will be established at a later stage.
(21)
1 kJ=0.239 kcal.
(22)
Amino acid content of foods and biological data on protein. FAO Nutritional Studies, No 24, Rome 1970, items 375 and 383.
(23)
SNF: “solids–no fats”.
(24)
NS: non specified, varies widely according to season and stock farming conditions.
