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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2015/1116 ,
Reg. (EU) No 540/2011
Date of approval 01/07/2015    
RMS Not Applicable Risk Assessment EFSA
Category FU Review Report   Review Report 2020
  Extension of use 2018
  Approval 2015
Type Basic substance    
Authorisation at national level
Not applicable
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Lecithins
    MRLs Annex IV
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI Not applicable Reg. (EU) 2015/1116  
ARfD Not applicable Reg. (EU) 2015/1116  
AOEL Not applicable Reg. (EU) 2015/1116  
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level