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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
DE

ES
Risk Assessment EFSA
Category HB Review Report   Comfirmatory data 2014
  Inclusion 2008
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
BE, BG, CZ, DE, EL, ES, FR, HU, IT, LU, NL, PL, PT, RO, SK AT, CY
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Sulcotrione (R)
    MRLs Annex II
Classification Reg. 1272/2008
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 0.0004 EFSA 08  
ARfD Not applicable EFSA 08  
AOEL 0.0006 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