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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/77/EC ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2010 Expiration of approval 31/12/2021
RMS

Co-RMS
SK

IT
Risk Assessment EFSA
Category IN Review Report
Remarks Extension of the approval period: Reg. (EU) 2017/555
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BG, CZ, DE, EL, ES, FR, HU, IT, MT, PL, RO, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Etofenprox (F)
    MRLs Annex II
Classification Reg. 1272/2008
Lact. - H362 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.03 EFSA 08  
ARfD 1 EFSA 08  
AOEL 0.06 EFSA 08  
Other
ADI= 0,03 (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