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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/66 ,
Reg. (EU) No 2018/1796 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2019
RMS

Co-RMS
AT

FI
Risk Assessment EFSA
Category HB Review Report
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LV, NL, PL, PT, RO, SE, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Fenoxaprop-P
    MRLs Annex IIIA
Classification Reg. 1272/2008
Skin Sens. 1 - H317 STOT RE 2 - H373
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 08/66  
ARfD 0.1 Dir 08/66  
AOEL 0.014 Dir 08/66  
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