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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2018/309 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation 03/39/EC ,
Reg. (EU) 2016/2016 ,
Reg.(EU) No 84/2018
    Expiration of approval 22/03/2018
RMS

Co-RMS
IT

RO
Risk Assessment Commission
Category FU Review Report   Non-renewal Report 2018
  Review Report 2003
Remarks Withdrawal authorisations: 22 June 2018

Max. period of grace: 22 June 2019
Authorisation at national level
Authorised in In progress for
BG, CY, CZ, EL, ES, HR, HU, IT, MT, PL, PT, RO, SI, SK
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
  • Propineb (expressed as propilendiamine)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Acute Tox. 4 - H332
STOT RE 2 - H373 Aquatic Acute 1 - H400
Toxicological information
Reference values Source Remark
ADI 0.007 Dir 03/39  
ARfD 0.1 Dir 03/39  
AOEL 0.003 Dir 03/39  
Other
PTU has ADI 0.0003 and ARfD 0.003 from same Directive ADI 0.007, ARfD 0.1 JMPR 2004 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level