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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2018/1532 Old Legislation 01/21/EC ,
2010/77/EU ,
Reg. (EU) 2015/1885 ,
Reg. (EU) 2016/549 ,
Reg. (EU) 2017/841 ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011
RMS

Co-RMS
UK

SE
Risk Assessment EFSA
Category HB, DE Review Report
Remarks Withdrawal authorisations by 4 May 2019.
Max period of grace: 4 February 2020.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Irrit. 2 - H315
Skin Sens. 1 - H317 Eye Irrit. 2 - H319
Acute Tox. 2 - H330 STOT SE 3 - H335
STOT RE 1 - H372 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.002 Dir 01/21  
ARfD Not applicable Dir 01/21  
AOEL 0.001 Dir 01/21  
Other
ADI 0.002 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