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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 496/2014 ,
Reg. (EU) No 540/2011
Old Legislation Dossier complete 03/636/EC
Date of approval 01/09/2014 Expiration of approval 31/08/2024
RMS

Co-RMS
DE

NL
Risk Assessment EFSA
Category AC Review Report
Remarks The original RMS were Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EL, FR, IT, LU, NL, PL, SI
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Acequinocyl
    MRLs Annex IIIA
Classification Reg. 1272/2008
Skin Sens. 1 - H317 STOT SE 1 - H370
STOT RE 2 - H373 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.023 Reg. (EU) No 496/2014  
ARfD 0.08 Reg. (EU) No 496/2014  
AOEL 0.014 Reg. (EU) No 496/2014  
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