Annex III to Regulation (EC) No 1333/2008 is amended in accordance with the Annex to this Regulation.
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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
This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Schedules & Appendices
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’
Cite this act
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 (EUR-Lex). Retrieved via LawPlayer, https://lawplayer.com/eu/act/32025R1150
© European Union, https://eur-lex.europa.eu, 1998-2026. Reuse authorised under Commission Decision 2011/833/EU, provided the source is acknowledged.
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