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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 149/2014 Old Legislation Dossier complete 05/751/EC
Date of approval 01/07/2014 Expiration of approval 30/06/2024
RMS

Co-RMS
NL

FR
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • L-ascorbic acid
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable EFSA 2013  
ARfD Not applicable EFSA 2013  
AOEL Not applicable EFSA 2013  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level