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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 04/60/EC ,
Reg. (EU) No 540/2011 ,
Reg.(EU)2018/524
Old Legislation Reg. (EU) 2016/2016
Date of approval 01/09/2004 Expiration of approval 30/04/2019
RMS

Co-RMS
UK

AT
Risk Assessment Commission
Category FU Review Report
Remarks Extension of the approval period (Reg. (EU) 2018/524)
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LU, MT, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Quinoxyfen (F)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.2 04/60/EC  
ARfD Not applicable 04/60/EC  
AOEL 0.14 04/60/EC  
Other
ARfD unnecessary ADI 0,2 JMPR 2006 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level