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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/68/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation Reg. (EU) 2016/950 ,
Reg. (EU) 2017/841
Date of approval 01/10/2003 Expiration of approval 31/07/2019
RMS

Co-RMS
IT

SI
Risk Assessment Commission
Category HB Review Report
Remarks The original RMS was the Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LU, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Isoxaflutole (sum of isoxaflutole and its diketonitrile-metabolite, expressed as isoxaflutole)
    MRLs Annex II
Classification Reg. 1272/2008
Repr. 2 - H361d Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.02 03/68/EC  
ARfD Not applicable 03/68/EC  
AOEL 0.02 03/68/EC  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level