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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/75/EC ,
Reg. (EU) No 1136/2013 ,
Reg. (EU) No 540/2011 ,
Reg.(EU) No 84/2018
   
Date of approval 01/10/2006 Expiration of approval 31/01/2019
RMS

Co-RMS
HU

IE
Risk Assessment EFSA
Category FU Review Report
Remarks

The original RMS was the UK.
Type Candidate for Substitution (CfS) CfS - criteria low ADI / ARfD / AOEL, two PBT criteria, endocrine disrupting properties
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, EE, FR, HR, HU, LT, LU, LV, PL, RO, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Dimoxystrobin (R) (A)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H332 Carc. 2 - H351
Repr. 2 - H361d Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.004 06/75/EC  
ARfD 0.004 06/75/EC  
AOEL 0.02 06/75/EC  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level