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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) 2019/344 Old Legislation 07/52/EC ,
Reg. (EU) 2018/917 ,
Reg. (EU) No 1178/2013 ,
Reg. (EU) No 540/2011
RMS

Co-RMS
IT

IE
Risk Assessment EFSA
Category NE, IN Review Report   Non renewal 2019
  Inclusion 2007
  Conditions of approval 2013
Remarks The original RMS was the UK.

Withdrawal of authorisations by 21 September 2019.
Max period of grace: 21 March 2020
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL
Authorisation at national level
Authorised in In progress for
CY, MT
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Ethoprophos
    MRLs Annex V
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 Reg. (EU) 2019/344 Not set due to insufficient data 
ARfD Reg. (EU) 2019/344 Not set due to insufficient data 
AOEL Reg. (EU) 2019/344 Not set due to insufficient data 
Other
ARfD 0,05 - ADI 0,0004 JMPR 2004 / Reference values previously established in EU  
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level