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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 03/70/EC ,
Reg. (EU) No 2016/2016 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012 ,
Reg.(EU) No 84/2018
   
Date of approval 01/06/2004 Expiration of approval 31/01/2019
RMS

Co-RMS
FI

UK
Risk Assessment Commission
Category FU Review Report   List of studies 2017
  Review Report 2003
Remarks Extension of the approval period (Reg. (EU) 84/2018)
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, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Propiconazole (sum of isomers) (F)
    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 0.04 Dir 03/70  
ARfD 0.3 Dir 03/70  
AOEL 0.1 Dir 03/70  
Other
ADI 0.07, ARfD 0.3 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