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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/107 ,
Reg. (EU) No 540/2011
   
Date of approval 01/05/2009 Expiration of approval 30/04/2019
RMS

Co-RMS
AT

DK
Risk Assessment EFSA
Category AC Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FR, HU, IT, PL, PT, RO, SE, SI, SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenpyroximate (A) (F) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Skin Sens. 1B - H317
Acute Tox. 2 - H330 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.01 EFSA 2013  
ARfD 0.02 EFSA 2013  
AOEL 0.005 EFSA 2013  
Other
ARfD 0,02 ADI 0,01 JMPR 2007 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level