Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses (Text with EEA relevance)
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Address https://gelex.eu/eli/EU/regulation/2009/953@2009-10-13/en
THE COMMISSION OF THE EUROPEAN COMMUNITIES,
Having regard to the Treaty establishing the European Community,
Having regard to Directive 2009/39/EC of the European Parliament and the Council of 6 May 2009 on foodstuffs intended for particular nutritional uses, and in particular Article 4(3) thereof,
After consulting the European Food Safety Authority,
Whereas:
(1) A number of nutritional substances such as vitamins, minerals, amino acids and others may be added to foods for particular nutritional uses in order to ensure that the particular nutritional requirements of the persons for whom those foods are intended are fulfilled and/or in order to satisfy legal requirements laid down in specific directives adopted pursuant to Article 4(1) of Directive 2009/39/EC. The list of those substances had been established by Commission Directive 2001/15/EC of 15 February 2001 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses and, following requests submitted by interested parties, new substances have been evaluated by the European Food Safety Authority, and consequently, that list should be completed and updated. Furthermore, it is appropriate to introduce specifications for some vitamin and mineral substances for their identification.
(2) It is neither possible to define nutritional substances as a distinct group for the purpose of this Regulation nor to draw up at this stage an exhaustive list of all categories of nutritional substances that may be added in foodstuffs for particular nutritional uses.
(3) The range of foods for particular nutritional uses is very wide and diversified and the technological processes used for their manufacture are varied. For this reason, the widest possible choice of substances that can be safely used in the manufacture of foods for particular nutritional uses should be available for the categories of nutritional substances to be listed in this Regulation.
(4) The choice of substances should be based primarily on their safety and subsequently on their availability for use by humans and on their organoleptic and technological properties. Unless otherwise specified in provisions applicable to specific categories of foodstuffs, the inclusion of substances in the list of those that may be used in the manufacture of foodstuffs for particular nutritional uses does not mean that their addition to those foodstuffs is necessary or desirable.
(5) Where the addition of a nutritional substance has been judged necessary, this has been stipulated by specific rules in the relevant specific directives together with the appropriate quantitative conditions, as the case may be.
(6) In the absence of any specific rules or in the case of foodstuffs for particular nutritional uses not covered by specific directives, nutritional substances should be used in order to manufacture products that are in conformity with the definition of such products and fulfil the particular nutritional requirements of the persons for whom they are intended. The products in question must also be safe when used as instructed by the manufacturer.
(7) The provisions concerning the list of the nutritional substances that may be used in the manufacture of infant formulae and follow-on formulae and of processed cereal-based foods and baby foods for infants and young children are laid down in Commission Directive 2006/141/EC of 22 December 2006 on infant formulae and follow-on formulae and amending Directive 1999/21/EC, and Commission Directive 2006/125/EC of 5 December 2006 on processed cereal-based foods and baby foods for infants and young children. Therefore those provisions need not be repeated in this Regulation.
(8) A number of the nutritional substances may be added for technological purposes as additives, colourings, flavourings or other such uses including authorised oenological practices and processes provided for by relevant Community legislation. In this context specifications are adopted for them at Community level. It is appropriate that those specifications should be applicable for the substances whatever the purpose of their use in foodstuffs.
(9) Pending the adoption of purity criteria for the rest of the substances at Community level, and in order to ensure a high level of protection for public health, generally acceptable purity criteria recommended by international organisations or agencies including but not limited to the Joint FAO/WHO Expert Committee on Food Additives (JECFA) and EUP (European Pharmacopoeia) should apply. Member States should be permitted to maintain national rules setting stricter purity criteria, without prejudice to the rules set out in the Treaty.
(10) Some specific nutrients or their derivatives have been identified as specifically necessary for the manufacture of some foodstuffs belonging to the group of foodstuffs for special medical purposes and their potential use should be reserved to the manufacture of these products.
(11) For the sake of clarity, Directive 2001/15/EC and Commission Directive 2004/6/EC of 20 January 2004 derogating from Directive 2001/15/EC to postpone the application of the prohibition of trade to certain products should be repealed and replaced by this Regulation.
(12) The measures provided in this Regulation are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health,
HAS ADOPTED THIS REGULATION:
Article 1 Scope
This Regulation shall apply to foods for particular nutritional uses, excluding those covered by Directive 2006/125/EC and Directive 2006/141/EC.
Article 2 Eligible substances
1. Among the substances belonging to the categories appearing in Annex to this Regulation, only those listed in that Annex, complying with the relevant specifications as necessary may be added for specific nutritional purposes in the manufacture of foodstuffs for particular nutritional uses covered by Directive 2009/39/EC.
2. Without prejudice to Regulation (EC) No 258/97 of the European Parliament and of the Council, also substances not belonging to the categories appearing in the Annex to this Regulation may be added for specific nutritional purposes in the manufacture of foods for particular nutritional uses.
Article 3 General requirements
1. The use of substances added for specific nutritional purposes shall result in the manufacture of safe products that fulfil the particular nutritional requirements of the persons for whom they are intended, as established by generally accepted scientific data.
2. Upon request by the competent authorities referred to in Article 11 of Directive 2009/39/EC, the manufacturer or, where appropriate, the importer shall produce the scientific work and the data establishing that the use of the substances complies with paragraph 1. If such work and data are contained in a readily available publication, a mere reference to that publication shall suffice.
Article 4 Specific requirements for substances listed in the Annex
1. The use of the substances listed in the Annex to this Regulation shall comply with any specific provisions concerning those substances that may be laid down in specific directives provided for in Article 4(1) of Directive 2009/39/EC.
2. Purity criteria established by Community legislation which apply to the substances listed in the Annex when they are used in the manufacture of foodstuffs for purposes other than those covered by this Regulation shall also apply to those substances when they are used for purposes covered by this Regulation.
3. For substances listed in the Annex for which purity criteria are not established by Community legislation, and until the adoption of such specifications, generally acceptable purity criteria recommended by international bodies shall apply. National rules setting stricter purity criteria may be maintained.
Article 5 Repeals
Directive 2001/15/EC and Directive 2004/6/EC are repealed with effect from 31 December 2009.
Article 6 Entry into force and application
This Regulation shall enter into force on the 20th day following its publication in the Official Journal of the European Union. It shall apply as from 1 January 2010.
This Regulation shall be binding in its entirety and directly applicable in all Member States. Done at Brussels, 13 October 2009. For the Commission Androulla Vassiliou Member of the Commission
ANNEX
ANNEX Substances that may be added for specific nutritional purposes in foods for particular nutritional uses Category 1.Category 2.Category 3.Category 4.Category 5.Category 6.
For the purpose of this table: Substance Condition of use Dietetic foods Foods for special medical purposes Vitamins VITAMIN A retinol x retinyl acetate x retinyl palmitate x beta-carotene x VITAMIN D cholecalciferol x ergocalciferol x VITAMIN E D-alpha-tocopherol x DL-alpha-tocopherol x D-alpha-tocopheryl acetate x DL-alpha-tocopheryl acetate x D-alpha-tocopheryl acid succinate x D-alpha-tocopheryl polyethylene glycol-1000 succinate (TPGS) x VITAMIN K phylloquinone (phytomenadione) x menaquinone x VITAMIN B1 thiamin hydrochloride x thiamin mononitrate x VITAMIN B2 riboflavin x riboflavin 5'-phosphate, sodium x NIACIN nicotinic acid x nicotinamide x PANTOTHENIC ACID D-pantothenate, calcium x D-pantothenate, sodium x dexpanthenol x VITAMIN B6 pyridoxine hydrochloride x pyridoxine 5'-phosphate x pyridoxine dipalmitate x FOLATE pteroylmonoglutamic acid x calcium-L-methylfolate x VITAMIN B12 cyanocobalamin x hydroxocobalamin x BIOTIN D-biotin x VITAMIN C L-ascorbic acid x sodium-L-ascorbate x calcium-L-ascorbate x potassium-L-ascorbate x L-ascorbyl 6-palmitate x Minerals CALCIUM calcium carbonate x calcium chloride x calcium salts of citric acid x calcium gluconate x calcium glycerophosphate x calcium lactate x calcium salts of orthophosphoric acid x calcium hydroxide x calcium oxide x calcium sulphate x calcium bisglycinate x calcium citrate malate x calcium malate x calcium L-pidolate x MAGNESIUM magnesium acetate x magnesium carbonate x magnesium chloride x magnesium salts of citric acid x magnesium gluconate x magnesium glycerophosphate x magnesium salts of orthophosphoric acid x magnesium lactate x magnesium hydroxide x magnesium oxide x magnesium sulphate x magnesium L-aspartate x magnesium bisglycinate x magnesium L-pidolate x magnesium potassium citrate x IRON ferrous carbonate x ferrous citrate x ferric ammonium citrate x ferrous gluconate x ferrous fumarate x ferric sodium diphosphate x ferrous lactate x ferrous sulphate x ferric diphosphate (ferric pyrophosphate) x ferric saccharate x elemental iron (carbonyl + electrolytic + hydrogen reduced) x ferrous bisglycinate x ferrous L-pidolate x COPPER cupric carbonate x cupric citrate x cupric gluconate x cupric sulphate x copper lysine complex x IODINE potassium iodide x potassium iodate x sodium iodide x sodium iodate x ZINC zinc acetate x zinc chloride x zinc citrate x zinc gluconate x zinc lactate x zinc oxide x zinc carbonate x zinc sulphate x zinc bisglycinate x MANGANESE manganese carbonate x manganese chloride x manganese citrate x manganese gluconate x manganese glycerophosphate x manganese sulphate x SODIUM sodium bicarbonate x sodium carbonate x sodium chloride x sodium citrate x sodium gluconate x sodium lactate x sodium hydroxide x sodium salts of orthophosphoric acid x POTASSIUM potassium bicarbonate x potassium carbonate x potassium chloride x potassium citrate x potassium gluconate x potassium glycerophosphate x potassium lactate x potassium hydroxide x potassium salts of orthophosphoric acid x magnesium potassium citrate x SELENIUM sodium selenate x sodium hydrogen selenite x sodium selenite x selenium enriched yeast x CHROMIUM (III) chromium (III) chloride and its hexahydrate x chromium (III) sulphate and its hexahydrate x MOLYBDENUM (VI) ammonium molybdate x sodium molybdate x FLUORINE potassium fluoride x sodium fluoride x BORON sodium borate x boric acid x Amino acids L-alanine x L-arginine x L-aspartic acid x L-citrulline x L-cysteine x Cystine x L-histidine x L-glutamic acid x L-glutamine x glycine x L-isoleucine x L-leucine x L-lysine x L-lysine acetate x L-methionine x L-ornithine x L-phenylalanine x L-proline x L-threonine x L-tryptophan x L-tyrosine x L-valine x L-serine x L-arginine-L-aspartate x L-lysine-L-aspartate x L-lysine-L-glutamate x N-acetyl-L-cysteine x N-acetyl-L-methionine x in products intended for persons over 1 year of age For amino acids, as far as applicable, also the sodium, potassium calcium and magnesium salts as well as their hydrochlorides may be used Carnitine and taurine L-carnitine x L-carnitine hydrochloride x taurine x L-carnitine-L-tartrate x Nucleotides adenosine 5'-phosphoric acid (AMP) x sodium salts of AMP x cytidine 5'-monophosphoric acid (CMP) x sodium salts of CMP x guanosine 5'-phosphoric acid (GMP) x sodium salts of GMP x inosine 5'-phosphoric acid (IMP) x sodium salts of IMP x uridine 5'-phosphoric acid (UMP) x sodium salts of UMP x Choline and inositol choline x choline chloride x choline bitartrate x choline citrate x inositol x
Dietetic foods means foods for particular nutritional uses including foods for special medical purposes but excluding infant formulae, follow-on formulae, processed cereal-based foods and baby foods intended for infants and young children,
Foods for special medical purposes means dietary foods for special medical purposes as defined in Commission Directive 1999/21/EC of 25 March 1999 on dietary foods for special medical purposes.
Versions
Cited by
- Commission Regulation (EU) No 1161/2011 of 14 November 2011 amending Directive 2002/46/EC of the European Parliament and of the Council, Regulation (EC) No 1925/2006 of the European Parliament and of the Council and Commission Regulation (EC) No 953/2009 as regards the lists of mineral substances that can be added to foods (Text with EEA relevance) Regulation · Grade B
The Annex to Commission Regulation (EC) No 953/2009 establishes the list of substances that may be added for specific nutritional purposes in foods for particular nutritional uses.
- Commission Regulation (EU) No 1161/2011 of 14 November 2011 amending Directive 2002/46/EC of the European Parliament and of the Council, Regulation (EC) No 1925/2006 of the European Parliament and of the Council and Commission Regulation (EC) No 953/2009 as regards the lists of mineral substances that can be added to foods (Text with EEA relevance) Regulation · Grade B
Directive 2002/46/EC, Regulation (EC) No 1925/2006 and Regulation (EC) No 953/2009 should therefore be amended accordingly.
- Commission Regulation (EU) No 1161/2011 of 14 November 2011 amending Directive 2002/46/EC of the European Parliament and of the Council, Regulation (EC) No 1925/2006 of the European Parliament and of the Council and Commission Regulation (EC) No 953/2009 as regards the lists of mineral substances that can be added to foods (Text with EEA relevance) Regulation · Grade B
Category 2 (Minerals) of the Annex to Regulation (EC) No 953/2009 is amended as follows:
- Regulation (EU) No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations (EC) No 41/2009 and (EC) No 953/2009 (Text with EEA relevance) Regulation · Grade B
In addition, harmonised rules are laid down in Council Directive 92/52/EEC of 18 June 1992 on infant formulae and follow-on formulae intended for export to third countries and in Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses.
- Regulation (EU) No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations (EC) No 41/2009 and (EC) No 953/2009 (Text with EEA relevance) Regulation · Grade B
Taking into account the existing situation on the market and Directives 2006/125/EC and 2006/141/EC, and Regulation (EC) No 953/2009, it is appropriate to establish and include in the Annex to this Regulation a Union list of substances belonging to the following categories of substances: vitamins, minerals, amino acids, carnitine and taurine, nucleotides, choline and inositol. Among the substances belonging to those categories, it should only be permissible for those included in the Union list to be added to the categories of food covered by this Regulation. When substances are included in the
- Regulation (EU) No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations (EC) No 41/2009 and (EC) No 953/2009 (Text with EEA relevance) Regulation · Grade B
Regulation (EC) No 953/2009 and Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC are repealed from the date of application of the delegated acts referred to in Article 11(1). In the case of conflict between Regulation (EC) No 953/2009, Directives 96/8/EC, 1999/21/EC, 2006/125/EC, 2006/141/EC and this Regulation, this Regulation shall prevail.
- Regulation (EU) No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations (EC) No 41/2009 and (EC) No 953/2009 (Text with EEA relevance) Regulation · Grade B
Food referred to in Article 1(1) of this Regulation which does not comply with this Regulation but complies with Directive 2009/39/EC, and, as applicable, with Regulation (EC) No 953/2009 and Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, and which is placed on the market or labelled before 20 July 2016 may continue to be marketed after that date until stocks of such food are exhausted. Where the date of application of the delegated acts referred to in Article 11(1) of this Regulation is after 20 July 2016, food referred to in Article 1(1) which complies with this Regulation and,
- Regulation (EU) No 609/2013 of the European Parliament and of the Council of 12 June 2013 on food intended for infants and young children, food for special medical purposes, and total diet replacement for weight control and repealing Council Directive 92/52/EEC, Commission Directives 96/8/EC, 1999/21/EC, 2006/125/EC and 2006/141/EC, Directive 2009/39/EC of the European Parliament and of the Council and Commission Regulations (EC) No 41/2009 and (EC) No 953/2009 (Text with EEA relevance) Regulation · Grade B
Food which is not referred to in Article 1(1) of this Regulation but which is placed on the market or labelled in accordance with Directive 2009/39/EC and Regulation (EC) No 953/2009, and, as applicable, with Directive 96/8/EC and Regulation (EC) No 41/2009 before 20 July 2016 may continue to be marketed after that date until stocks of such food are exhausted.
- Commission Decision of 25 November 2010 authorising the placing on the market of ferrous ammonium phosphate as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 8191) (Only the French text is authentic) (2010/715/EU) Decision · Grade B
Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses, Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the approximation of the laws of the Member States relating to food supplements and/or Regulation (EC) No 1925/2006 of the European Parliament and of the Council of 20 December 2006 on the addition of vitamins and minerals and of certain other substances to foods lay down specific provision for the use of vitamins, minerals and other substances i
- Commission Decision of 25 November 2010 authorising the placing on the market of ferrous ammonium phosphate as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 8191) (Only the French text is authentic) (2010/715/EU) Decision · Grade B
Ferrous ammonium phosphate as a source of iron as specified in the Annex may be placed on the market in the Union as a novel food ingredient to be used in food without prejudice to the specific provisions of Regulation (EC) No 953/2009, Directive 2002/46/EC and/or Regulation (EC) No 1925/2006.
- Commission Decision of 14 June 2010 authorising the placing on the market of Ferric Sodium EDTA as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 3729) (Only the German text is authentic) (2010/331/EU) Decision · Grade B
Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses, Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the approximation of the laws of the Member States relating to food supplements and/or Regulation (EC) No 1925/2006 of the European Parliament and of the Council of 20 December 2006 on the addition of vitamins and minerals and of certain other substances to foods lay down specific provision for the use of vitamins, minerals and other substances i
- Commission Decision of 14 June 2010 authorising the placing on the market of Ferric Sodium EDTA as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 3729) (Only the German text is authentic) (2010/331/EU) Decision · Grade B
Ferric Sodium EDTA as a source of iron as specified in the Annex I may be placed on the market in the Union as a novel food ingredient to be used in food without prejudice to the specific provisions of Regulation (EC) No 953/2009, Directive 2002/46/EC and/or Regulation (EC) No 1925/2006. The maximum amount of Ferric Sodium EDTA (expressed as anhydrous EDTA) to be used in foods is set out in Annex II.
- Commission Decision of 14 June 2010 authorising the placing on the market of Ferric Sodium EDTA as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 3729) (Only the German text is authentic) (2010/331/EU) Decision · Grade B
Ferric Sodium EDTA (ethylenediaminetetraacetic acid) is an odourless free-flowing, yellow to brown powder with a chemical purity of more than 99 % (w/w). It is freely soluble in water. CAS No 18154-32-0 (CAS anhydrous 15708-41-5) Chemical Formula C10H12FeN2NaO8 * 3H2O Structural Formula Chemical characteristics of Ferric Sodium EDTA without prejudice to the provisions of Regulation (EC) No 953/2009, Directive 2002/46/EC and/or Regulation (EC) No 1925/2006 pH of 1 % solution 3,5 to 5,5 Iron 12,5 % to 13,5 % Sodium 5,5 % Water 12,8 % Organic matter (CHNO) 68,4 % EDTA 65,5 % to 70,5 % Water insol
- Commission Decision of 14 June 2010 authorising the placing on the market of Ferric Sodium EDTA as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2010) 3729) (Only the German text is authentic) (2010/331/EU) Decision · Grade B
Food supplements (in accordance with Directive 2002/46/EC) children: 18 mg per daily dose as recommended by the manufacturer adults: 75 mg per daily dose as recommended by the manufacturer Dietetic foods (in accordance with Regulation (EC) No 953/2009) 12 mg EDTA per 100 g of final food Fortified foods (in accordance with Regulation (EC) No 1925/2006) 12 mg EDTA per 100 g of final food
- Council Decision (EU) 2016/877 of 23 May 2016 on the position to be adopted, on behalf of the European Union, within the Sanitary and Phytosanitary Subcommittee established by the Association Agreement between the European Union and the European Atomic Energy Community and their Member States, of the one part, and the Republic of Moldova, of the other part Decision · Grade B
In accordance with Article 181(4) of this Agreement, the Republic of Moldova shall approximate its legislation to the following Union legislation within the timeframes as listed below. Union legislation Deadline for approximation Section 1 — General Regulation (EC) No 178/2002 of the European Parliament and of the Council of 28 January 2002 laying down the general principles and requirements of food law, establishing the European Food Safety Authority and laying down procedures in matters of food safety, with the exception of Articles 58, 59 and 62 2016 Commission Regulation (EC) No 1304/2003
- Commission Regulation (EU) No 1130/2011 of 11 November 2011 amending Annex III to Regulation (EC) No 1333/2008 of the European Parliament and of the Council on food additives by establishing a Union list of food additives approved for use in food additives, food enzymes, food flavourings and nutrients (Text with EEA relevance) Regulation · Grade B
Food additives and carriers authorised for use in nutrients defined by Regulation (EC) No 1925/2006 of the European Parliament and of the Council of 20 December 2006 on the addition of vitamins and minerals and of certain other substances to foods as well as by Directive 2002/46/EC of the European Parliament and of the Council of 10 June 2002 on the approximation of the laws of the Member States relating to food supplements, Directive 2009/39/EC of the European Parliament and of the Council of 6 May 2009 on foodstuffs intended for particular nutritional uses, and Commission Regulation (EC) No
- Commission Regulation (EU) No 1130/2011 of 11 November 2011 amending Annex III to Regulation (EC) No 1333/2008 of the European Parliament and of the Council on food additives by establishing a Union list of food additives approved for use in food additives, food enzymes, food flavourings and nutrients (Text with EEA relevance) Regulation · Grade B
nutrients for the purposes of this Annex means vitamins, minerals and other substances added for nutritional purposes, as well as substances added for physiological purposes as covered by Regulation (EC) No 1925/2006, Directive 2002/46/EC, Directive 2009/39/EC and Regulation (EC) No 953/2009. preparation for the purposes of this Annex means a formulation consisting of one or more food additives, food enzymes and/or nutrients in which substances such as food additives and/or other food ingredients are incorporated to facilitate their storage, sale, standardisation, dilution or dissolution.
- Commission Decision of 27 May 2011 authorising the placing on the market of Chromium Picolinate as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2011) 3586) (Only the English text is authentic) (2011/320/EU) Decision · Grade B
Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses and/or Regulation (EC) No 1925/2006 of the European Parliament and of the Council of 20 December 2006 on the addition of vitamins and minerals and of certain other substances to foods lay down specific provisions for the use of vitamins, minerals and other substances in food. The use of Chromium Picolinate should be authorised without prejudice to the requirements of this legislation.
- Commission Decision of 27 May 2011 authorising the placing on the market of Chromium Picolinate as a novel food ingredient under Regulation (EC) No 258/97 of the European Parliament and of the Council (notified under document C(2011) 3586) (Only the English text is authentic) (2011/320/EU) Decision · Grade B
Chromium Picolinate as a source of chromium as specified in the Annex may be placed on the market in the Union as a novel food ingredient to be used in food without prejudice to the specific provisions of Regulation (EC) No 953/2009 and/or Regulation (EC) No 1925/2006.
- Judgment of the Court (Fifth Chamber) of 5 November 2014 (request for a preliminary ruling from the Bayerisches Verwaltungsgericht München — Germany) — Herbaria Kräuterparadies GmbH v Freistaat Bayern (Case C-137/13) Notice · Grade B
Directive 2009/39/EC of the European Parliament and of the Council of 6 May 2009 on foodstuffs intended for particular nutritional uses and Commission Regulation (EC) No 953/2009 of 13 October 2009 on substances that may be added for specific nutritional purposes in foods for particular nutritional uses; that foodstuff must contain a determined quantity of the substance in question.