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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/72/EC ,
Reg. (EU) 2016/2035 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 762/2013
   
Date of approval 01/07/2006 Expiration of approval 31/01/2017
RMS

Co-RMS
IT

UK
Risk Assessment Commission
Category FU Review Report
Remarks Amendment of the approval period (Reg. (EU) 2016/2035)
Authorisation at national level
Authorised in In progress for
BE, NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dithiocarbamates (dithiocarbamates expressed as CS2, including maneb, mancozeb, metiram, propineb, thiram and ziram)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Eye Irrit. 2 - H319
Acute Tox. 4 - H332 Repr. 2 - H361d
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.05 Dir 05/72  
ARfD 0.2 Dir 05/72  
AOEL 0.03 Dir 05/72  
Other
ADI 0,03 JMPR 1993 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level