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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/16/EC ,
Reg. (EU) No 1136/2013 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 84/2018
   
Date of approval 01/08/2006 Expiration of approval 31/01/2019
RMS

Co-RMS
IT

FR
Risk Assessment EFSA
Category IN, NE Review Report
Remarks
The original RMS was Ireland.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
BE, BG, CY, CZ, EL, ES, FR, HR, HU, IE, IT, MT, NL, PL, PT, RO, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
Classification Reg. 1272/2008
Acute Tox. 2 - H300 Acute Tox. 4 - H312
Acute Tox. 2 - H330 Aquatic Chronic 2 - H411
Toxicological information
Reference values Source Remark
ADI 0.001 Dir 06/16  
ARfD 0.001 Dir 06/16  
AOEL 0.001 Dir 06/16  
Other
ARfD 0,009 - ADI 0,009 JMPR 2002 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level