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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/41/EC ,
Reg. (EU) No 1136/2013 ,
Reg. (EU) No 2018/1264 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 84/2018
   
Date of approval 01/08/2006 Expiration of approval 31/01/2019
RMS

Co-RMS
AT

CZ
Risk Assessment EFSA
Category HB Review Report   Renewal Repor 2018
  List of studies 2017
  Review Report 2006
Remarks The original RMS was Germany.

Reg. (EU) No 2018/1264 renewing the approval of pethoxamid shall apply from 1 December 2018
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, EL, ES, FR, HR, HU, IT, LU, PL, PT, RO, SI, SK, UK BG
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Pethoxamid
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Skin Sens. 1 - H317
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.01 Reg. (EU) No 2018/1264  
ARfD 0.08 Reg. (EU) No 2018/1264  
AOEL 0.02 Reg. (EU) No 2018/1264  
Other
AAOEL: 0.08 mg/kg bw per day 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level