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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2018/1914 Old Legislation 04/60/EC ,
Reg. (EU) 2016/2016 ,
Reg. (EU) No 540/2011 ,
Reg.(EU)2018/524
RMS

Co-RMS
UK

AT
Risk Assessment EFSA
Category FU Review Report   Review Report 2018
  Review Report 2003
Remarks Non-renewal of approval voted in October 2018.
Withdrawal authorisations by 27 June 2019.
Max period of grace:27 March 2020.

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 Reg. (EU) 2018/1914  
ARfD Not applicable Reg. (EU) 2018/1914  
AOEL 0.14 Reg. (EU) 2018/1914  
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