PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 07/52/EC ,
Reg. (EU) 1178/2013 ,
Reg. (EU) 2018/917 ,
Reg. (EU) 540/2011
   
Date of approval 01/10/2007 Expiration of approval 31/07/2019
RMS

Co-RMS
IT

IE
Risk Assessment EFSA
Category NE, IN Review Report   Inclusion 2007
  Conditions of approval 2013
Remarks The original RMS was the UK.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
BE, BG, CY, EL, ES, IE, IT, MT, NL, UK PT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Ethoprophos
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 1 - H310
Skin Sens. 1 - H317 Acute Tox. 2 - H330
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0004 Reg. (EU) No 1178/2013  
ARfD 0.01 Reg. (EU) No 1178/2013  
AOEL 0.001 Reg. (EU) No 1178/2013  
Other
ARfD 0,05 - ADI 0,0004 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