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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 705/2011 Old Legislation 1997/73/EC ,
2007/21/EC ,
2010/57/EU ,
Reg. (EU) No 540/2011
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
NL

BE
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2015
  Renewal 2011
  Inclusion 1997
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, NL, PL, PT, RO, SE, UK LV
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Imazalil
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Eye Dam. 1 - H318
Acute Tox. 4 - H332 Carc. 2 - H351
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.025 EFSA 2010  
ARfD 0.05 EFSA 2010  
AOEL 0.05 EFSA 2010  
Other
ADI 0.03 JMPR 2001 ARfD 0.05 JMPR 2005 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level