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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2011/5/EU ,
Reg.(EU) No 2018/1266 ,
Reg.(EU) No 540/2011
   
Date of approval 01/06/2011 Expiration of approval 31/05/2023
RMS

Co-RMS
AT

SE
Risk Assessment EFSA
Category FU Review Report   Confirmatory data 2014
  Inclusion 2011
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, EL, ES, FI, FR, HU, IE, IT, NL, PL, RO, SE, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Hymexazol
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Eye Dam. 1 - H318
Aquatic Chronic 3 - H412  
Toxicological information
Reference values Source Remark
ADI 0.17 EFSA 10  
ARfD 0.5 EFSA 10  
AOEL 0.17 EFSA 10  
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