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Regulation 3(1)

SCHEDULE 1U.K.Regulations Revoked

Regulation revokedReference:
Cosmetic Products (Safety) Regulations 2008S.I. 2008/1284
Cosmetic Products (Safety) (Amendment) Regulations 2008S.I. 2008/2173
Cosmetic Products (Safety) (Amendment No. 2) Regulations 2008S.I. 2008/2566
Cosmetic Products (Safety) (Amendment) Regulations 2009S.I. 2009/796
Cosmetic Products (Safety) (Amendment No. 2) Regulations 2009S.I. 2009/1346
Cosmetic Products (Safety) (Amendment No. 3) Regulations 2009S.I. 2009/2562
Cosmetic Products (Safety) (Amendment No. 4) Regulations 2009S.I. 2009/3367
Cosmetic Products (Safety) (Amendment) Regulations 2010S.I. 2010/1150
Cosmetic Products (Safety) (Amendment No. 2) Regulations 2010S.I. 2010/1927
Cosmetic Products (Safety) (Amendment) Regulations 2011S.I. 2011/3037
The Cosmetic Products (Safety) (Amendment) Regulations 2012S.I. 2012/2263

Regulation 7(1)(a)

F1SCHEDULE 2U.K.Testing, powers of entry etc and warrants

. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .

Regulation 7(2)

SCHEDULE 3U.K.Sampling and Testing

1.  In this Schedule—U.K.

Annex A” means the Annex to Commission Directive No 80/1335/EEC M1 as amended by Commission Directive No 87/143/EEC M2;

Annex B” means the Annex to Commission Directive No 82/434/EEC M3 as amended by Commission Directive No 90/207/EEC M4;

Annex C” means the Annex to Commission Directive No 83/514/EEC M5;

Annex D” means the Annex to Commission Directive No 85/490/EEC M6;

Annex E” means the Annex to Commission Directive No 93/73/EEC M7;

Annex F” means the Annex to Commission Directive No 95/32/EC M8;

Annex G” means the Annex to Commission Directive No 96/45/EC M9;

purchase” means purchase for the purpose of carrying out a test.

Marginal Citations

M1OJ No L 383, 31.12.80, p 27–46.

M2OJ No L 57, 27.2.87, p 56.

M3O.J. No L 185, 30.6.82, p 27–46.

M4OJ L 108, 28.4.90, p 1–28.

M5OJ No L 291, 24.10.83, p 9–46.

M6OJ No L 295, 7.11.85, p 30–45.

M7OJ No L 231, 14.9.93.

M8OJ No L 178, 28.7.95.

M9OJ No L 213, 22.8.96, p 8.

2.  An enforcement authority intending to purchase a cosmetic product must purchase a sufficient laboratory sample, as defined in paragraph 2.3 of Part 1 of Annex A, for the purpose of Annex A; and, for the purposes of the definition of “total sample” in paragraph 2.2 of Part 1 of Annex A; samples shall be regarded as having the sample batch number if—U.K.

(a)the means of identifying the batch referred to in Article 19(1)(e) of the [F2EU] Cosmetics Regulation shows that they were manufactured in the same batch;

(b)in the case of a product not manufactured in a batch, the reference referred to in Article 19(1)(e) of the [F2EU] Cosmetics Regulation shows that they are derived from the same unit of production; or

(c)in the case of a product which does not comply with the requirements of Article 19(1)(e) of the [F2EU] Cosmetics Regulation, the officer effecting the purchase has reasonable cause to believe that they were manufactured in the same batch or are derived from the same unit of production, as the case may be.

Textual Amendments

3.  The immediate container, if any, of a cosmetic product purchased by an enforcement authority must not be opened by, on behalf of or at the request of the enforcement authority before the purchase takes place and the container must not thereafter be opened except in accordance with paragraph 5.3 of Part I of Annex A and paragraph 1.2 of Part II of Annex A.U.K.

4.  As soon as an enforcement authority has purchased a cosmetic product, the officer effecting the purchase must—U.K.

(a)either—

(i)place a seal on the product's container or outer packaging; or

(ii)place the product in a container and immediately place a seal on that container, in such a way that the product's immediate container cannot be opened or (in the case of a product which was not in a container when it was purchased) the product cannot be touched without (in either case) the seal being broken in such a manner that it would be apparent thereafter that it had been broken, and

(b)attach to the product a label indicating—

(i)the name of the product,

(ii)the date, time and place at which the product was purchased,

(iii)the name of the officer, and

(iv)the name of the enforcement authority making the purchase.

5.—(1) Subject to sub-paragraph (2), the provisions of Part 1 of Annex A, other than paragraphs 3.1, 3.2 and 4, and of Part II of Annex A, other than paragraph 1.4, must be complied with in the sampling of cosmetic products and the laboratory preparation of test portions.U.K.

(2) Where, because of the way in which a cosmetic product is put up for sale, it is not practicable for Part II of Annex A to be complied with, it must be prepared for testing in accordance with good analytical practice, and the person so preparing it must record in writing the method of preparation which has been used.

6.—(1) Any test to determine whether a cosmetic product contains a significant amount of free sodium hydroxide or free potassium hydroxide must be carried out in accordance with paragraphs 1 to 4 of Part III of Annex A.U.K.

(2) Any test to determine the amount of free sodium hydroxide or free potassium hydroxide in a hair straightener product or a nail cuticle solvent product must be carried out in accordance with paragraphs 1, 2, 3 and 5 of Part III of Annex A.

(3) Any test to determine whether a hair-care product contains oxalic acid or any alkaline salt of oxalic acid or to determine the amount of such a substance in a hair-care product must, subject to the limitation specified in the second sentence of paragraph 1 of Part IV of Annex A, be carried out in accordance with the said Part IV.

(4) Any test to determine the amount of chloroform in toothpaste must, subject to the limitation specified in the second sentence of paragraph 1 of Part V of Annex A, be carried out in accordance with the said Part V.

(5) Any test to determine the amount of zinc chloride, zinc sulphate or zinc 4-hydroxybenzene- sulphonate by virtue of their zinc contents in a cosmetic product must be carried out in accordance with Part VI of Annex A and Commission Directive 87/143/EEC M10, and must take into account paragraph 11 of Part VII of Annex A.

(6) Any test to determine whether a cosmetic product contained in an aerosol dispenser or a cream, emulsion, lotion, gel or oil intended to be applied to the skin contains 4-hydroxybenzene-sulphonic acid, or to determine the amount of that acid in such a product, must be carried out in accordance with Part VII of Annex A.

(7) Any test to determine whether a hair-care product contains persulphate, bromate or hydrogen peroxide must be carried out in accordance with Part A of Part I of Annex B.

(8) Any test to determine whether a hair-care product contains barium peroxide must be carried out in accordance with Part B of Part 1 of Annex B.

(9) Any test to determine the amount of hydrogen peroxide in a hair-care product must be carried out in accordance with Part C of Part I of Annex B.

(10) Any test to determine whether a hair dye contains any of the oxidation colourants specified in paragraph 1 of Part II of Annex B, or to determine the amount of such a substance in a hair-dye, must be carried out in accordance with the said Part II.

(11) Any test to determine whether a cosmetic product contains nitrite, or to determine the amount of that substance in a cosmetic product, must be carried out in accordance with Part III of Annex B.

(12) Any test to determine whether a cosmetic product contains free formaldehyde, or to determine the amount of that substance in a cosmetic product, must be carried out in accordance with Part IV of Annex B.

(13) Any test to determine the amount of resorcinol in a shampoo or hair lotion must, subject to the limitation specified in the second sentence of paragraph 1 of Part V of Annex B, be carried out in accordance with the said Part V.

(14) Any test to determine the amount of methanol in relation to ethanol or propan-2-ol in a cosmetic product must be carried out in accordance with Part VI of Annex B.

(15) Any test to determine the amount of dichloromethane or 1,1,1-trichloroethane in a cosmetic product must be carried out in accordance with paragraphs 1 to 10 of that part of Annex C which is headed “Determination of dichloromethane and 1,1,1-trichloroethane”.

(16) Any test to determine whether a cosmetic product contains quinolin-8-ol or bis(8-hydroxyquinolinium) sulphate, or to determine the amount of such a substance in a cosmetic product, must be carried out in accordance with paragraphs 1 to 9 of that part of Annex C which is headed “Identification and determination of quinolin-8-ol-and bis(8-hydroxyquinolinium) sulphate”.

(17) Any test to determine the amount of ammonia in a cosmetic product must be carried out in accordance with paragraphs 1 to 8 of that part of Annex C which is headed “Determination of ammonia”.

(18) Any test to determine whether a cosmetic product contains nitromethane, or to determine the amount of that substance in a cosmetic product, must be carried out in accordance with paragraphs 1 to 7 of that part of Annex C which is headed “Identification and determination of nitromethane”.

(19) Any test to determine whether a hair waving, hair straightening or depilatory product contains mercaptoacetic acid (thioglycolic acid), or to determine the amount of that substance in such a product, must be carried out in accordance with paragraphs 1 to 6 of that part of Annex C which is headed “Identification and determination of mercaptoacetic acid in hair waving, hair straightening and depilatory products”.

(20) Any test to determine whether a cosmetic product contains hexachlorophene (INN) must be carried out in accordance with paragraphs 1 to 7 of Part A of that part of Annex C which is headed “Identification and determination of hexachlorophene”.

(21) Any test to determine the amount of hexachlorophene (INN) in a cosmetic product must be carried out in accordance with paragraphs 1 to 9 of Part B of that part of Annex C which is headed “Identification and determination of hexachlorophene”.

(22) Any test to determine the amount of tosylchloramide sodium (INN) in a cosmetic product must be carried out in accordance with paragraphs 1 to 9 of that part of Annex C which is headed “Quantitative determination of tosylchloramide sodium (INN) (chloramine-T)”.

(23) Any test to determine the total amount of fluorine in dental creams must be carried out in accordance with paragraphs 1 to 8 of that part of Annex C which is headed “Determination of total fluorine in dental creams”.

(24) Any test to determine whether a cosmetic product contains organomercury compounds must be carried out in accordance with paragraphs 1 to 4 of Part A of that part of Annex C which is headed “Identification and determination of organomercury compounds”.

(25) Any test to determine the amount of organomercury compounds in a cosmetic product must be carried out in accordance with paragraphs 1 to 7 of Part B of that part of Annex C which is headed “Identification and determination of organomercury compounds”.

(26) Any test to determine the amount of alkali sulphides or alkaline earth sulphides in a cosmetic product must be carried out in accordance with paragraphs 1 to 8 of that part of Annex C which is headed “Determination of alkali and alkaline earth sulphides”.

(27) Any test for the identification and determination of the amount of glycerol 1-(4-aminobenzoate) in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Identification and determination of glycerol 1-(4-aminobenzoate)”.

(28) Any test to determine the amount of chlorobutanol (INN) in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Determination of chlorobutanol”.

(29) Any test for the identification and determination of the amount of quinine in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Identification and determination of quinine”.

(30) Any test for the identification and determination of inorganic sulphites and hydrogen sulphites in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Identification and determination of inorganic sulphites and hydrogen sulphites”.

(31) Any test for the identification and determination of chlorates of the alkali metals in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Identification and determination of chlorates of the alkali metals”.

(32) Any test for the identification and determination of sodium iodate in a cosmetic product must be carried out in accordance with that part of Annex D which is headed “Identification and determination of sodium iodate”.

(33) Any test for the identification and determination of silver nitrate in a cosmetic product must be carried out in accordance with that part of Annex E which is headed “Identification and determination of silver nitrate in cosmetic products”.

(34) Any test for the identification and determination of selenium disulphide in anti-dandruff shampoos must be carried out in accordance with that part of Annex E which is headed “Identification and determination of selenium disulphide in anti-dandruff shampoos”.

(35) Any test for the determination of soluble barium and soluble strontium in pigments in the form of salts or lakes must be carried out in accordance with that part of Annex E which is headed “Determination of soluble barium and strontium in pigments in the form of salts or lakes”.

(36) Any test for the identification and determination of benzyl alcohol in a cosmetic product must be carried out in accordance with that part of Annex E which is headed “Identification and determination of benzyl alcohol in cosmetic products”.

(37) Any test for the identification of zirconium and the determination of zirconium, aluminium and chlorine in non-aerosol anti-perspirants must be carried out in accordance with that part of Annex E which is headed “identification of zirconium, and determination of zirconium, aluminium and chlorine in non-aerosol anti-perspirants”.

(38) Any test for the identification and determination of hexamidine, dibromohexamidine, dibromopropamidine and chlorhexidine in a cosmetic product must be carried out in accordance with that part of Annex E which is headed “Identification and determination of hexamidine, dibromohexamidine, dibromopropamidine and chlorhexidine”.

(39) Any test for the identification and determination of benzoic acid, 4-hydroxybenzoic acid, sorbic acid, salicylic acid and propionic acid in a cosmetic product must be carried out in accordance with that part of Annex F which is headed “Identification and determination of benzoic acid, 4-hydroxybenzoic acid, sorbic acid, salicylic acid and propionic acid in cosmetic products”.

(40) Any test for the identification and determination of hydroquinone, hydroquinone monomethyl ether, hydroquinone monoethyl ether and hydroquinone monobenzyl ether (monobenzone) in a cosmetic product must be carried out in accordance with that part of Annex F which is headed “Identification and determination of hydroquinone, hydroquinone monomethyl ether, hydroquinone monoethyl ether and hydroquinone monobenzyl ether in cosmetic products”.

Any test for the identification and determination of 2-phenoxyethanol, 1-phenoxypropan-2-ol, and methyl, ethyl, propyl, butyl and benzyl 4-hydroxybenzoate in a cosmetic product must be carried out in accordance with Annex G.

Marginal Citations

M10OJ No L 057, 27.02.87, p 56.

Regulation 12(1)

SCHEDULE 4U.K.Offences for Breach for the EU Cosmetics Regulation

Provision of the EU Cosmetics RegulationSubject Matter
Article 3Safety
Article 5Obligations of responsible persons
Article 6Obligations of distributors
Article 7Identification within the supply chain
Article 10Safety assessment
Article 11Requirements for the product information file
Article 13Notification requirements
Article 14Restrictions for substances listed in the Annexes
Article 15Substances classified as CMR substances
Article 16Notification requirements in relation to nanomaterials
Article 18Animal testing requirements
Article 19Labelling requirements
Article 20Requirements relating to product claims
Article 21Access to information for the public
Article 23Communication of serious undesirable effects
Article 24Information requirements on substances

Regulation 25

SCHEDULE 5U.K.Consequential Amendments

Weights and Measures (Northern Ireland) Order 1981U.K.

1.  Part 5 of Schedule 6 to the Weights and Measures (Northern Ireland) Order 1981 M11 is repealed.

Marginal Citations

M11S.I. 1981/231 (NI 10), amended by S.R. (NI) 1994 No 319; there are other amending instruments but none is relevant.

2.  In paragraph 3 of Part 6 of Schedule 6 to the Weights and Measures (Northern Ireland) Order 1981—U.K.

(a)omit “as defined in paragraph 1 of Part V”;

(b)the existing provision becomes sub-paragraph (1);

(c)at the end insert—

(2) Cosmetic product” has the same meaning as in Regulation (EC) 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time.

Weights and Measures Act 1985U.K.

3.  Part 5 of Schedule 6 to the Weights and Measures Act 1985 M12 is repealed.

Marginal Citations

M121985 c. 72; amended by S.I. 1994/1884; there are other amending instruments but none is relevant.

4.  In paragraph 16A of Schedule 6 to the Weights and Measures Act 1985—U.K.

(a)omit “as defined in paragraph 15 above”;

(b)the existing provision becomes sub-paragraph (1);

(c)at the end insert—

(2) Cosmetic product” has the same meaning as in Regulation (EC) 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time.

Control of Pesticides Regulations 1986U.K.

5.  In regulation 3(2)(b)(iv) of the Control of Pesticides Regulations 1986 M13 for “the Cosmetic Products (Safety) Regulations 1984” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time. ”

Marginal Citations

M13S.I. 1986/1510, amended by S.I. 1997/188; there are other amending instruments but none is relevant.

Control of Pesticides Regulations (Northern Ireland) 1987U.K.

6.  In regulation 3(2)(b)(iv) of the Control of Pesticides Regulations (Northern Ireland) 1987 M14 for “the Cosmetic Products (Safety) Regulations 1984” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time. ”

Marginal Citations

M14S.R. (NI) 1987 No 414; amended by S.R. NI 1997 No 469; there are other amending instruments but none is relevant.

Dangerous Substances in Harbour Areas Regulations 1987U.K.

7.  In regulation 3(3)(c) of the Dangerous Substances in Harbour Areas Regulations 1987 M15 for “regulation 4(1) of the Cosmetic Products (Safety) Regulations 1984” substitute “ Article 2(1)(a) of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

M15S.I. 1987/37, to which there are amendments not relevant to these Regulations.

Dangerous Substances in Harbour Areas Regulations (Northern Ireland) 1991U.K.

8.  In regulation 3(3)(c) of the Dangerous Substances in Harbour Areas Regulations (Northern Ireland) 1991 M16 for “regulation 4(1) of the Cosmetic Products (Safety) Regulations 1984” substitute “ Article 2(1)(a) of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

M16S.R. (NI) 1991 No 509, to which there are amendments not relevant to these Regulations.

Patents (Licences of Right) (Exception of Pesticidal Use) Order 1989U.K.

9.  In article 2(2)(bb) of the Patents (Licences of Right) (Exception of Pesticidal Use) Order 1989 M17 for “the Cosmetics Products (Safety) Regulations 1984” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

M17S.I. 1989/1202, as amended by SI 1990/2487.

Water Protection Zone (River Dee Catchment) Designation Order 1999U.K.

10.  In article 2(1) of the Water Protection Zone (River Dee Catchment) Designation Order 1999 M18 for “Cosmetic Products (Safety) Regulations 1996” from sub-paragraph (g) of the definition of “controlled substance” and substitute “Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time”.

Marginal Citations

M18S.I. 1999/915, to which there are amendments not relevant to these Regulations.

Biocidal Products Regulations (Northern Ireland) 2001U.K.

11.  In Schedule 2 of the Biocidal Products Regulations (Northern Ireland) 2001 M19

(a)omit “the Cosmetic Products (Safety) Regulations 1996”;

(b)insert “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ” in the appropriate place.

Marginal Citations

M19S.R (NI) 2001 No 422.

Biocidal Products Regulations 2001U.K.

12.  In Schedule 2 of the Biocidal Products Regulations 2001 M20

(a)omit “the Cosmetic Products (Safety) Regulations 1996”;

(b)insert “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ” in the appropriate place.

Marginal Citations

M20S.I. 2001/880, to which there are amendments not relevant to these Regulations.

Control of Substances Hazardous to Health Regulations 2002U.K.

13.  In the definition of “cosmetic product” in Schedule 2 of the Control of Substances Hazardous to Health Regulations 2002 M21 for “regulation 2(1) of the Cosmetic Products (Safety) Regulations 1996” substitute “ Article 2 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) as amended from time to time ”.

Marginal Citations

M21S.I. 2002/2677, to which there are amendments not relevant to these Regulations.

Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003U.K.

14.  In the definition of “cosmetic product” in Schedule 2 of the Control of Substances Hazardous to Health Regulations (Northern Ireland) 2003 M22 for “regulation 2(1) of the Cosmetic Products (Safety) Regulations 1996” substitute “ Article 2 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) as amended from time to time ”.

Marginal Citations

M22S.R. (NI) 2003 No 34, to which there are amendments not relevant to these Regulations.

Good Laboratory Practice (Codification Amendments Etc.) Regulations 2004U.K.

15.  Omit regulation 4 of the Good Laboratory Practice (Codification Amendments Etc.) Regulations 2004 M23.

Marginal Citations

Enterprise Act 2002 (Part 9 Restrictions on Disclosure of Information) (Specification) Order 2004U.K.

16.  At the end of Schedule 1 to the Enterprise Act 2002 (Part 9 Restrictions on Disclosure of Information) (Specification) Order 2004 M24 insert “ The Cosmetic Products Enforcement Regulations 2013 ”.

Marginal Citations

M24S.I. 2004/693, to which there are amendments not relevant to these Regulations.

Weights and Measures (Packaged Goods) Regulations 2006U.K.

17.  The Weights and Measures (Packaged Goods) Regulations 2006 M25 are amended as follows—

(a)in the definition of “cosmetic product” in regulation 2, for “regulation 3 of the Cosmetic Products (Safety) Regulations 2004” substitute “ Article 2 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) as amended from time to time ”;

(b)in regulation 5(7) for “regulation 7(2)(a) of the Cosmetic Products (Safety) Regulations 2004 requires a package to be marked with information about the manufacturer or supplier established in a member State” substitute “ Article 19 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time, requires a package to bear information about the responsible person, as defined in Article 4 of that Regulation ”;

(c)in regulation 6(6) for “regulation 7(2)(a) of the Cosmetic Products (Safety) Regulations 2004 requires an outer container to be marked with information about the manufacturer or supplier established in a member State” substitute “ Article 19 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) as amended from time to time, requires an outer container to bear information about the responsible person, as defined in Article 4 of that Regulation ”.

Marginal Citations

Legislative and Regulatory Reform (Regulatory Functions) Order 2007U.K.

18.  The Legislative and Regulatory Reform (Regulatory Functions) Order 2007 M26, is amended as follows.

Marginal Citations

M26S.I. 2007/3544, amended by S.I. 2009/2981; there are other amending instruments but none is relevant.

19.  In Part 3 of Schedule 1, under the heading “Consumer and business protection”—U.K.

(a)omit “Cosmetic Products (Safety) Regulations 2008”;

(b)insert “ the Cosmetic Products Enforcement Regulations 2013 ” at the appropriate place.

20.  In Part 8 of Schedule 1—U.K.

(a)omit “Cosmetic Products (Safety) Regulations 2008”;

(b)insert “ the Cosmetic Products Enforcement Regulations 2013 ” in the appropriate place.

21.  In Part 13 of Schedule 1—U.K.

(a)omit “Cosmetic Products (Safety) Regulations 2008”;

(b)insert “ the Cosmetic Products Enforcement Regulations 2013 ” in the appropriate place.

Chemicals (Hazard Information and Packaging for Supply) Regulations (Northern Ireland) 2009U.K.

22.  In regulation 3(2)(f) of the Chemicals (Hazard Information and Packaging for Supply) Regulations (Northern Ireland) 2009 M27 for “the Cosmetic Products (Safety) Regulations 2008” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

M27S.R. (NI) 2009 No 238, to which there are amendments not relevant to these Regulations.

Explosives (Hazard Information and Packaging for Supply) Regulations (Northern Ireland) 2009U.K.

23.  In regulation 3(2)(f) of the Explosives (Hazard Information and Packaging for Supply) Regulations (Northern Ireland) 2009 M28 for “the Cosmetic Products (Safety) Regulations 2008” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

M28S.R. (NI) 2009 No 273.

Co-ordination of Regulatory Enforcement (Regulatory Functions in Scotland and Northern Ireland) Order 2009U.K.

24.  The Co-ordination of Regulatory Enforcement (Regulatory Functions in Scotland and Northern Ireland) Order 2009 M29 is amended as follows.

Marginal Citations

25.  In Part 4 of Schedule 1 paragraph 1—U.K.

(a)omit “Cosmetic Products (Safety) Regulations 2008”;

(b)insert “ Cosmetic Products Enforcement Regulations 2012 ” in the appropriate place;

26.  In Part 2 of Schedule 2, paragraph 1—U.K.

(a)omit “Cosmetic Products (Safety) Regulations 2008”

(b)insert “ Cosmetic Products Enforcement Regulations 2012 ” in the appropriate place.

Chemicals (Hazard Information and Packaging for Supply) Regulations 2009U.K.

27.  In regulation 3(2)(f) of the Chemicals (Hazard Information and Packaging for Supply) Regulations 2009 M30 for “the Cosmetic Products (Safety) Regulations 2008” substitute “ Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast), as amended from time to time ”.

Marginal Citations

Pharmacy Order 2010U.K.

28.  In Schedule 4, Part 2, of the Pharmacy Order 2010 M31 omit paragraph 65.

Marginal Citations

Weights and Measures (Packaged Goods) Regulations (Northern Ireland) 2011U.K.

29.  The Weights and Measures (Packaged Goods) Regulations (Northern Ireland) 2011 M32 are amended as follows—

(a)in Regulation 2 in the definition of “cosmetic product” for “regulation 3 of the Cosmetic Products (Safety) Regulations 2008” substitute “ Article 2 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) as amended from time to time ”;

(b)in Regulation 5(7) for “Where regulation 12(1)(a) of the Cosmetic Products (Safety) Regulations 2008 requires a package to be marked with information about the manufacturer or supplier established in a member State” substitute “ Where Article 19 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) M33 requires a package to bear information about the responsible person, as defined in Article 4 of that Regulation ”;

(c)in Regulation 6(6) for “Where regulation 12(1)(a) of the Cosmetic Products (Safety) Regulations 2008 requires an outer container to be marked with information about the manufacturer or supplier established in a member State” substitute “ Where Article 19 of Regulation (EC) No 1223/2009 of the European Parliament and of the Council on cosmetic products (recast) M34 requires a container to bear information about the responsible person, as defined in Article 4 of that Regulation ”.

Marginal Citations

M32S.R. (NI) 2011 No 331.

M33OJ No L 342, 22.12.2009, p.59.

M34OJ No L 342, 22.12.2009, p.59.

Animal By-Products (Enforcement) (England) Regulations 2011U.K.

30.  In Schedule 2 of Animal By-Products (Enforcement) (England) Regulations 2011 M35 omit paragraph 16.

Marginal Citations

Animal By-Products (Enforcement) (No. 2) (Wales) Regulations 2011U.K.

31.  In Schedule 2 of Animal By-Products (Enforcement) (No. 2) (Wales) Regulations 2011 M36 omit paragraph 15.

Marginal Citations

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