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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/934 ,
2010/455/EU
   
RMS UK

Risk Assessment EFSA
Category FU, RE    
Remarks Withdrawal authorisations: 31/12/2011. Max period of grace: 31/12/2012.
Authorisation at national level
No authorisation in place
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Guazatine (guazatine acetate, sum of components)
    MRLs Annex V
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H312
Skin Irrit. 2 - H315 Eye Dam. 1 - H318
Acute Tox. 2 - H330 STOT SE 3 - H335
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.0048 EFSA 10  
ARfD 0.04 EFSA 10  
AOEL 0.002 EFSA 10  
Other
JMPR 1997 - No ADI 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level