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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/2/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2021
RMS

Co-RMS
AT

ES
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2016
  Inclusion 2011
Remarks Initially non included by Decision 2008/934. Included as from 1 June 2011 following re-submission for inclusion according to Reg. 33/2008

The original RMS was UK.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EL, ES, FR, HR, HU, IE, IT, LU, MT, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Myclobutanil (R)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Eye Irrit. 2 - H319
Repr. 2 - H361d Aquatic Chronic 2 - H411
Toxicological information
Reference values Source Remark
ADI 0.025 EFSA 10  
ARfD 0.31 EFSA 10  
AOEL 0.03 EFSA 10  
Other
ADI 0,03 JMPR 1998 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level