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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/108 ,
Reg. (EU) No 540/2011
   
Date of approval 01/03/2009 Expiration of approval 28/02/2019
    Risk Assessment EFSA
Category HB Review Report   Inclusion 2008
  Confirmatory data 2012
Remarks The RMS is Norway

The CO-RMS is Netherlands

Authorisation at national level
Authorised in In progress for
BE, CY, EL, ES, FR, HU, IE, IT, NL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Benfluralin (F)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.005 Dir 08/108  
ARfD Not applicable Dir 08/108  
AOEL 0.005 Dir 08/108  
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