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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 540/2011 ,
Reg. (EU) No 84/2018 ,
Reg.(EU) 2018/692
Old Legislation 03/119/EC ,
Reg. (EU) No 2016/2016 ,
Reg. (EU) No 823/2012
Date of approval 01/07/2018 Expiration of approval 30/06/2033
RMS

Co-RMS
LV

FR
Risk Assessment EFSA
Category FU Review Report   Volume 2, May 2017
  Renewal Report 2018
  Review Report 2003
Remarks The original RMS was the UK.


Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EL, ES, FR, HR, HU, IE, IT, LT, LV, MT, NL, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Zoxamide
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.5 Reg. (EU) 2018/692  
ARfD Not applicable Reg. (EU) 2018/692  
AOEL 0.3 Reg. (EU) 2018/692  
Other
ADI 0,5 ARfD unnecessary JMPR 2007 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level