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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/70 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2010 Expiration of approval 31/12/2020
RMS

Co-RMS
FR

SI
Risk Assessment EFSA
Category FU, AC, RE Review Report   Inclusion 2009
  Revision 2012
Remarks Extension of the approval period: Reg. (EU) 2017/555
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FR, HR, HU, IE, IT, LU, 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
Skin Irrit. 2 - H315
Toxicological information
Reference values Source Remark
ADI Not applicable EFSA 08  
ARfD Not applicable EFSA 08  
AOEL Not applicable EFSA 08  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level