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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/125 ,
Reg. (EU) 2017/195 ,
Reg. (EU) No 540/2011
   
Date of approval 01/09/2009 Expiration of approval 31/08/2022
RMS

Co-RMS
NL

IT
Risk Assessment EFSA
Category FU Review Report
Authorisation at national level
Authorised in In progress for
EL, IT, NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
Classification Reg. 1272/2008
Skin Corr. 1C - H314 Skin Sens. 1A - H317
Repr. 2 - H361d STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.082 EFSA 08  
ARfD 0.33 EFSA 08  
AOEL 0.033 Dir 08/125  
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