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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/5/EC ,
Reg. (EU) 187/2014 ,
Reg. (EU) 2018/917 ,
Reg. (EU) 540/2011
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
UK

DE
Risk Assessment EFSA
Category IN, RE Review Report   Conditions of approval 2014
  Inclusion 2007
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, HR, HU, IE, IT, LU, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Methiocarb (sum of methiocarb and methiocarb sulfoxide and sulfone, expressed as methiocarb)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.013 Dir 07/5  
ARfD 0.013 Dir 07/5  
AOEL 0.013 Dir 07/5  
Other
ARfD 0,02 - ADI 0,02 JMPR 2005 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level