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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/41/EC ,
Reg. (EU) No 2018/1264 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 1136/2013 ,
Reg. (EU) No 84/2018
Date of approval 01/12/2018 Expiration of approval 30/11/2033
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.

Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EL, ES, FR, HR, HU, IT, LU, PL, PT, RO, SI, SK, UK
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