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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/86/EU ,
Reg. (EU) 2015/2233 ,
Reg. (EU) No 2018/670 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2011 Expiration of approval 31/12/2023
RMS

Co-RMS
HU

CZ
Risk Assessment EFSA
Category HB Review Report   Conditions of approval 2016
  Inclusion 2010
Remarks Austria was assigned as Designated Member State (DMS) to assess confirmatory data
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, HU, LU, NL, PL, RO, SK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Haloxyfop (Sum of haloxyfop, its esters, salts and conjugates expressed as haloxyfop (sum of the R- and S- isomers at any ratio)) (F) (R)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.00065 Reg. (EU) 2015/2233  
ARfD 0.075 Reg. (EU) 2015/2233  
AOEL 0.005 Reg. (EU) 2015/2233  
Other
ADI 0,0007 ARfD 0,08 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