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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 540/2011 ,
Reg. (EU) No 542/2011
Old Legislation 2006/135/EC ,
2010/70/EC ,
2011/58/EU
Date of approval 01/01/2007 Expiration of approval 30/11/2014
RMS DE

Risk Assessment EFSA
Category FU Review Report   renewal 2011
  inclusion 2007
Remarks Max. period of grace: 31/05/2016.
Authorisation at national level
No authorisation in place
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Carbendazim and benomyl (sum of benomyl and carbendazim expressed as carbendazim) (R)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Muta. 1B - H340 Repr. 1B - H360FD
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.02 Dir 06/135  
ARfD 0.02 Dir 06/135  
AOEL 0.02 Dir 06/135  
Other
ARfD 0,5 - ADI 0,03 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