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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/77/EC ,
2010/34/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2010 Expiration of approval 31/12/2021
    Risk Assessment EFSA
Category FU Review Report   Specifications 2009
  Extension of inclusion 2010
Remarks RMS is Norway.

Extension of the approval period: Reg. (EU) 2017/555
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, EE, EL, ES, FI, FR, HR, HU, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Penconazole (F)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Repr. 2 - H361d
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 Dir 09/77  
ARfD 0.5 Dir 09/77  
AOEL 0.03 Dir 09/77  
Other
ADI= 0,03 JMPR 1992 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level