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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/5/EC ,
Reg.(EU) 2018/917 ,
Reg.(EU) 540/2011
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
AT

IT
Risk Assessment EFSA
Category FU Review Report
Remarks The original RMS was Italy.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Folpet (sum of folpet and phtalimide, expressed as folpet) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Eye Irrit. 2 - H319
Acute Tox. 4 - H332 Carc. 2 - H351
Aquatic Acute 1 - H400  
Toxicological information
Reference values Source Remark
ADI 0.1 Dir 07/5  
ARfD 0.2 SCoFCAH July 08  
AOEL 0.1 Dir 07/5  
Other
ARfD 0,2 (women of child-bearing age) - ADI 0,1 JMPR 2004 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level