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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 2018/1266 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 87/2012
Old Legislation 2008/934/EC ,
2011/21/EU
Date of approval 01/06/2011 Expiration of approval 31/05/2023
RMS

Co-RMS
SE

LT
Risk Assessment EFSA
Category HB Review Report   Confirmatory data 2014
  Revision Dec 2011
  Inclusion 2011
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Clethodim (sum of Sethoxydim and Clethodim including degradation products calculated as Sethoxydim)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
Aquatic Chronic 3 - H412  
Toxicological information
Reference values Source Remark
ADI 0.16 EFSA 11  
ARfD Not applicable EFSA 11  
AOEL 0.2 EFSA 11  
Other
ADI 0,01 ARfD unnecessary JMPR 1999 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level