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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/81/EC ,
Reg. (EU) No 540/2011 ,
Reg. (Eu) 2018/1500 ,
Reg.(EU)2018/524
Old Legislation Reg. (EU) 2016/2016
RMS

Co-RMS
FR

BE
Risk Assessment EFSA
Category FU Review Report   Final Renewal Report 2018
  List of Studies 2017
  Review report 2003
Remarks The original RMS was Belgium.
Non-renewal of approval: Reg. (EU) 2018/1500
Withdrawal of authorisations by 30 January 2019.
Max period of grace: 30 April 2019 for PPPs used for foliar appliacation and 30 January 2020 for other PPPs (for seed treatment included)
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FR, HR, HU, IE, IT, LT, LV, NL, PL, PT, RO, SI, SK, UK
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
  • Thiram (expressed as thiram)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Irrit. 2 - H315
Skin Sens. 1 - H317 Eye Irrit. 2 - H319
Acute Tox. 4 - H332 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 Reg. (Eu) 2018/1500  
ARfD 0.025 Reg. (Eu) 2018/1500  
AOEL 0.02 Reg. (Eu) 2018/1500  
Other
AAOEL: 0.025 mg/kg bw 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level