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(EU) No 957/2010:批准和拒绝某些用于食品涉及降低疾病风险和儿童成长、健康有关的声称(on the authorisation and refusal of authorisation of certain health claims made on foods and referring to the reduction of disease risk and to children’s development and health)

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核心提示?010?0?3日,欧盟发布委员会条?EU) No 957/2010,批?种食品健康声称,分别如下?)碘有助于儿童正常生长。该声称仅限用于符合(EC) No 1924/2006附录所列“维生素名称?或矿物质名称”来源声称要求的至少可作为碘来源的食品?)铁有助于儿童正常的认知发育。该声称仅限用于符合(EC) No 1924/2006附录所列“维生素名称?或矿物质名称”来源声称要求的至少可作为铁来源的食品。同时,拒绝批准3种食品健康声称、/div>
发布单位
EUROPEAN COMMISSION
EUROPEAN COMMISSION
发布文号 (EU) No 957/2010
发布日期 暂无 生效日期 暂无
有效性状?/th> 废止日期 暂无
备注 2010?0?3日,欧盟发布委员会条?EU) No 957/2010,批?种食品健康声称,分别如下?)碘有助于儿童正常生长。该声称仅限用于符合(EC) No 1924/2006附录所?ldquo;维生素名称和/或矿物质名称来源声称要求的至少可作为碘来源的食品?)铁有助于儿童正常的认知发育。该声称仅限用于符合(EC) No 1924/2006附录所?ldquo;维生素名称和/或矿物质名称来源声称要求的至少可作为铁来源的食品。同时,拒绝批准3种食品健康声称,分别如下?)原花青素经证实可减低血液胆固醇含量,从而降低冠心病风险?)食品补充剂Uroval?的主要活性成?mdash;蔓越莓提取物和D-甘露糖,可消除有害细菌在膀胱壁上的粘着力。有害细菌粘着于膀胱壁上是泌尿道感染的主要风险因素?)双歧杆菌(两歧双歧杆菌、短双岐杆菌、婴儿双歧杆菌和长双歧杆菌)组合产品:双歧益生菌有助于形成与母乳喂养婴儿肠道的肠道菌群组分相差无几的健康肠道菌群、/td>

  COMMISSION REGULATION (EU) No 957/2010

  of 22 October 2010

  on the authorisation and refusal of authorisation of certain health claims made on foods and referring to the reduction of disease risk and to childrens development and health

  (Text with EEA relevance)

  THE EUROPEAN COMMISSION,

  Having regard to the Treaty on the Functioning of the European Union,

  Having regard to Regulation (EC) No 1924/2006 of the European Parliament and of the Council of 20 December 2006 on nutrition and health claims made on foods (1), and in particular Article 17(3) thereof,

  Whereas:

  (1)

  Pursuant to Regulation (EC) No 1924/2006 health claims made on food are prohibited unless they are authorised by the Commission in accordance with that Regulation and included in a list of permitted claims.

  (2)

  Regulation (EC) No 1924/2006 also provides that applications for authorisations of health claims may be submitted by food business operators to the national competent authority of a Member State. The national competent authority is to forward valid applications to the European Food Safety Authority (EFSA), hereinafter referred to as the Authority.

  (3)

  Following receipt of an application the Authority is to inform without delay the other Member States and the Commission of the application, and to deliver an opinion on a health claim concerned.

  (4)

  The Commission is to decide on the authorisation of health claims taking into account the opinion delivered by the Authority.

  (5)

  Two opinions referred to in this Regulation are related to applications for reduction of disease risk claims, as referred to in Article 14(1)(a) of Regulation (EC) No 1924/2006 and three opinions are related to applications for health claims referring to childrens development and health, as referred to in Article 14(1)(b) of Regulation (EC) No 1924/2006.

  (6)

  Following an application from Association de la Transformation Laitire Fran?aise (ATLA), submitted pursuant to Article 14(1)(b) of Regulation (EC) No 1924/2006, the Authority was required to deliver an opinion on a health claim related to the effects of iodine on normal growth of children (Question No EFSA-Q-2008-324) (2). The claim proposed by the applicant was worded as follows: Iodine is necessary for the growth of children.

  (7)

  On the basis of the data presented, the Authority concluded in its opinion received by the Commission and the Member States on 20 November 2009 that a cause and effect relationship had been established between the intake of iodine and the claimed effect. Accordingly, a health claim reflecting this conclusion should be considered as complying with the requirements of Regulation (EC) No 1924/2006, and it should be included in the Union list of permitted claims.

  (8)

  Following an application from Association de la Transformation Laitire Fran?aise (ATLA), submitted pursuant to Article 14(1)(b) of Regulation (EC) No 1924/2006, the Authority was required to deliver an opinion on a health claim related to the effects of iron on cognitive development of children (Question No EFSA-Q-2008-325) (3). The claim proposed by the applicant was worded as follows: Iron is necessary for the cognitive development of children.

  (9)

  On the basis of the data presented, the Authority concluded in its opinion received by the Commission and the Member States on 20 November 2009 that a cause and effect relationship had been established between the intake of iron and the claimed effect. Accordingly, a health claim reflecting this conclusion should be considered as complying with the requirements of Regulation (EC) No 1924/2006, and it should be included in the Union list of permitted claims.

  (10)

  Article 16(4) of Regulation (EC) No 1924/2006 provides that an opinion in favour of authorising a health claim should include certain particulars. Accordingly, those particulars should be set out in the Annex I to the present Regulation as regards the authorised claims and include, as the case may be, the revised wording of the claims, specific conditions of use of the claims, and, where applicable, conditions or restrictions of use of the food and/or an additional statement or warning, in accordance with the rules laid down in Regulation (EC) No 1924/2006 and in line with the opinions of the Authority.

  (11)

  One of the objectives of Regulation (EC) No 1924/2006 is to ensure that health claims are truthful, clear and reliable and useful to the consumer, and that wording and presentation are taken into account in that respect. Therefore, where the wording of claims has the same meaning for consumers as that of an authorised health claim, because they demonstrate the same relationship that exists between a food category, a food or one of its constituents and health, they should be subject to the same conditions of use, as indicated in Annex I.

  (12)

  Following an application from GP International Holding BV, submitted pursuant to Article 14(1)(a) of Regulation (EC) No 1924/2006, the Authority was required to deliver an opinion on a health claim related to the effects of OPC PremiumTM on reduction of blood cholesterol (Question No EFSA-Q-2009-00454) (4). The claim proposed by the applicant was worded as follows: OPC have been shown to reduce blood cholesterol levels and may therefore reduce the risk of cardiovascular disease.

  (13)

  On the basis of the data presented, the Authority concluded in its opinion received by the Commission and the Member States on 26 October 2009 that a cause and effect relationship had not been established between the intake of OPC PremiumTM and the claimed effect. Accordingly, as the claim does not comply with the requirements of Regulation (EC) No 1924/2006, it should not be authorised.

  (14)

  Following an application from Valosun AS, submitted pursuant to Article 14(1)(a) of Regulation (EC) No 1924/2006, the Authority was required to deliver an opinion on a health claim related to the effects of Uroval? on urinary tract infections (Question No EFSA-Q-2009-00600) (5). The claim proposed by the applicant was worded as follows: Cranberry extract and D-mannose, the main active ingredients of the food supplement Uroval?, eliminate the adhesion of harmful bacteria to the bladder wall. The adhesion of harmful bacteria to the bladder wall is the main risk factor in the development of urinary tract infections.

  (15)

  On the basis of the data presented, the Authority concluded in its opinion received by the Commission and the Member States on 22 December 2009 that a cause and effect relationship had not been established between the intake of Uroval? and the claimed effect. Accordingly, as the claim does not comply with the requirements of Regulation (EC) No 1924/2006, it should not be authorised.

  (16)

  Following an application from T?pfer GmbH, submitted pursuant to Article 14(1)(b) of Regulation (EC) No 1924/2006, the Authority was required to deliver an opinion on a health claim related to the effects of a combination of bifidobacteria (Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium infantis, Bifidobacterium longum) on decreasing potentially pathogenic intestinal micro-organisms (Question No EFSA-Q-2009-00224) (6). The claim proposed by the applicant was worded as follows: Probiotic bifidobacteria lead to a healthy intestinal flora comparable to the composition of the intestinal flora of breast-fed infants intestine.

  (17)

  On the basis of the data presented, the Authority concluded in its opinion received by the Commission and the Member States on 22 December 2009 that a cause and effect relationship had not been established between the intake of the combination of bifidobacteria and the claimed effect. Accordingly, as the claim does not comply with the requirements of Regulation (EC) No 1924/2006, it should not be authorised.

  (18)

  The comments from the applicants and the members of the public received by the Commission pursuant to Article 16(6) of Regulation (EC) No 1924/2006 have been considered when setting the measures provided for in this Regulation.

  (19)

  The measures provided for in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health and neither the European Parliament nor the Council have opposed them,

  HAS ADOPTED THIS REGULATION:

  Article 1

  The health claims set out in Annex I to this Regulation may be made on foods on the European Union market in compliance with the conditions set out in that Annex.

  Those health claims shall be included in the Union list of permitted claims referred to in Article 14(1) of Regulation (EC) No 1924/2006.

  Article 2

  The health claims set out in Annex II to this Regulation shall not be included in the Union list of permitted claims as provided for in Article 14(1) of Regulation (EC) No 1924/2006.

  Health claims as referred to in Article 14(1)(b) of Regulation (EC) No 1924/2006 and set out in Annex II to this Regulation may continue to be used for six months after the entry into force of this Regulation.

  Article 3

  This Regulation shall enter into force on the 20th day following its publication in the Official Journal of the European Union.

  This Regulation shall be binding in its entirety and directly applicable in all Member States.

  Done at Brussels, 22 October 2010.

  For the Commission

  The President

  Jos Manuel BARROSO

ANNEX I
Permitted health claims
Application Relevant provisions of Regulation (EC) No 1924/2006
Applicant Address
Nutrient, substance, food or food category
Claim
Conditions of use of the claim
Conditions and/or restrictions of use of the food and/or additional statement or warning
EFSA opinion reference
Article 14(1)(b) health claim referring to childrens development and health
Association de la Transformation Laitire Fran?aise (ATLA), 42 rue de Ch?teaudun, 75314 Paris Cedex 09, France
Iodine
Iodine contributes to the normal growth of children
The claim can be used only for food which is at least a source of iodine as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006
Q-2008-324
Article 14(1)(b) health claim referring to childrens development and health
Association de la Transformation Laitire Fran?aise (ATLA), 42 rue de Ch?teaudun, 75314 Paris Cedex 09, France
Iron
Iron contributes to normal cognitive development of children
The claim can be used only for food which is at least a source of iron as referred to in the claim SOURCE OF [NAME OF VITAMIN/S] AND/OR [NAME OF MINERAL/S] as listed in the Annex to Regulation (EC) No 1924/2006
Q-2008-325


ANNEX II
Rejected health claims
Application Relevant provisions of Regulation (EC) No 1924/2006
Nutrient, substance, food or food category
Claim
EFSA opinion reference
Article 14(1)(a) health claim referring to a reduction of a disease risk
OPC Premium?
OPC have been shown to reduce blood cholesterol levels and may therefore reduce the risk of cardiovascular disease
Q-2009-00454
Article 14(1)(a) health claim referring to a reduction of a disease risk
Uroval?
Cranberry extract and D-mannose, the main active ingredients of the food supplement Uroval?, eliminate the adhesion of harmful bacteria to the bladder wall. The adhesion of harmful bacteria to the bladder wall is the main risk factor in the development of urinary tract infections
Q-2009-00600
Article 14(1)(b) health claim referring to childrens development and health
Combination of bifidobacteria (Bifidobacterium bifidum, Bifidobacterium breve, Bifidobacterium infantis, Bifidobacterium longum)
Probiotic bifidobacteria lead to a healthy intestinal flora comparable to the composition of the intestinal flora of breast-fed infants intestine
Q-2009-00224
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