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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2009/25/EC ,
Reg. (EU) No 2018/1796 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 823/2012
Old Legislation 2004/30/EC ,
Reg. (EU) No 2016/2016 ,
Reg.(EU) No 84/2018
Date of approval 01/06/2004 Expiration of approval 31/01/2020
RMS

Co-RMS
DE

HU
Risk Assessment Commission
Category FU, PG Review Report
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, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
Skin Irrit. 2 - H315 Acute Tox. 3 - H331
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.03 04/30/EC  
ARfD 0.03 04/30/EC  
AOEL 0.015 04/30/EC  
Other
ARfD 0,05 - ADI 0,03 JMPR 2004 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level