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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 30/12/2019
RMS

Co-RMS
IT

PT
Risk Assessment EFSA
Category RO Review Report   Inclusion 2009
  Revision 2012
  Revision 2011
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria
Authorisation at national level
Authorised in In progress for
PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Default MRL of 0.01 mg/kg according to Art 18(1)(b) Reg 396 / 2005.
Classification Reg. 1272/2008
Acute Tox. 1 - H300 Acute Tox. 1 - H310
Acute Tox. 1 - H330 Repr. 1B - H360D
STOT RE 1 - H372 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI Not applicable EFSA 08  
ARfD Not applicable EFSA 08  
AOEL 0.000017 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