Directive 2009/163 - Amendment of Directive 94/35/EC on sweeteners for use in foodstuffs with regard to neotame - Main contents
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official title
Commission Directive 2009/163/EU of 22 December 2009 amending Directive 94/35/EC of the European Parliament and of the Council on sweeteners for use in foodstuffs with regard to neotame| Legal instrument | Directive |
|---|---|
| Number legal act | Directive 2009/163 |
| CELEX number i | 32009L0163 |
| Document | 22-12-2009 |
|---|---|
| Publication in Official Journal | 23-12-2009; OJ L 344, 23.12.2009,Special edition in Croatian: Chapter 13 Volume 043 |
| Effect | 12-01-2010; Entry into force Date pub. + 20 See Art 3 |
| End of validity | 20-01-2010; Implicitly repealed by 32008R1333 |
| Transposition | 12-10-2010; At the latest See Art 2.1 |
23.12.2009 |
EN |
Official Journal of the European Union |
L 344/37 |
COMMISSION DIRECTIVE 2009/163/EU
of 22 December 2009
amending Directive 94/35/EC of the European Parliament and of the Council on sweeteners for use in foodstuffs with regard to neotame
(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 1333/2008 of the European Parliament and of the Council of 16 December 2008 on food additives (1), and in particular Article 31 thereof,
After consulting the European Food Safety Authority (EFSA),
Whereas:
(1) |
Directive 94/35/EC of the European Parliament and of the Council of 30 June 1994 on sweeteners for use in foodstuffs (2) lays down a list of sweeteners that may be used in the Union and the conditions for their use. |
(2) |
The European Food Safety Authority (EFSA) evaluated the safety of neotame as a sweetener and flavour enhancer and expressed its opinion of 27 September 2007 (3). After considering all the data on stability, degradation products and toxicology, EFSA concluded that neotame is not of safety concern with respect to the proposed uses as a sweetener and flavour enhancer and established an acceptable daily intake (ADI) of 0–2 mg/kg bw/day. EFSA also noted that conservative estimates of neotame dietary exposure both in adults and children suggest that it is very unlikely that the ADI would be exceeded at the proposed use levels. |
(3) |
Neotame is a highly intense sweetener with a sweetness potency ranging from 7 000 to 13 000 times that of sucrose. It may be used as a replacement for sucrose or other sweeteners in a broad range of products. Neotame can be used alone or with other sweeteners. In addition, neotame can modify the flavour of foods and beverages. |
(4) |
It is necessary to amend the Annex of Directive 94/35/EC to permit the use of neotame in the same food applications as the other currently permitted intense sweeteners. Neotame should be assigned a new E number, namely E 961. In order to facilitate the marketing and use of this new sweetener, it is provided that products which comply with the provisions of this Directive may be marketed from the date of its entry into force. |
(5) |
In accordance with point 34 of the Interinstitutional agreement on better law-making (4), Member States are encouraged to draw up, for themselves and in the interests of the Union, their own tables, which will, as far as possible, illustrate the correlation between this Directive and the transposition measures, and to make them public. |
(6) |
The measures provided for in this Directive are in accordance with the opinion of the Standing Committee on the Food Chain and Animal Health, |
HAS ADOPTED THIS DIRECTIVE:
Article 1
The Annex to Directive 94/35/EC is amended in accordance with the Annex to this Directive.
Article 2
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1.Member States shall bring into force the laws, regulations and administrative provisions necessary to comply with this Directive by 12 October 2010 at the latest. They shall forthwith communicate to the Commission the text of those provisions.
When Member States adopt those provisions, they shall contain a reference to this Directive or be accompanied by such a reference on the occasion of their official publication. Member States shall determine how such reference is to be made.
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2.Member States shall communicate to the Commission the text of the main provisions of national law which they adopt in the field covered by this Directive.
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3.Products which comply with the provisions of this Directive may be marketed from the date of entry into force of this Directive.
Article 3
This Directive shall enter into force on the 20th day following its publication in the Official...
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