Article 1
Open ↗Annex III to Regulation (EC) No 1333/2008 is amended in accordance with the Annex to this Regulation.
Source
Commission Regulation (EU) 2025/1150 of 11 June 2025 amending Annex III to Regulation (EC) No 1333/2008 of the European Parliament and of the Council as regards the use of sodium ascorbate (E 301) in vitamin A preparations intended for infant formula and follow-on formula
Commission Regulation (EU) 2025/1150 of 11 June 2025 amending Annex III to Regulation (EC) No 1333/2008 of the European Parliament and of the Council as regards the use of sodium ascorbate (E 301) in vitamin A preparations intended for infant formula and follow-on formula
Data as of 2026-07-04 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
Open ↗This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX In Section B of Part 5 of Annex III to Regulation (EC) No 1333/2008, the entry for food additive E 301 is replaced by the following: ‘E 301 Sodium ascorbate 100 000 mg/kg in vitamin D preparation and 1 mg/l maximum carry-over in final food Vitamin D preparations Infant formula and follow-on formula as defined by Regulation (EU) No 609/2013 50 000 mg/kg in microencapsulated vitamin A preparation and 1 mg/l maximum carry-over in final food Microencapsulated vitamin A preparations Infant formula and follow-on formula as defined by Regulation (EU) No 609/2013 Total carry-over 75 mg/l Coatings of nutrient preparations containing polyunsaturated fatty acids Foods for infants and young children’
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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