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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation Reg. (EU) No 797/2011 Old Legislation 2007/21/EC ,
99/73/EC ,
Reg. (EU) No 540/2011
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
AT

EE
Risk Assessment EFSA
Category FU Review Report   Renewal 2011
  Inclusion 1999
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FR, HR, HU, IE, IT, LT, LU, LV, PL, PT, RO, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Spiroxamine (sum of isomers) (A) (R)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H312
Skin Irrit. 2 - H315 Skin Sens. 1 - H317
Acute Tox. 4 - H332 Repr. 2 - H361d
STOT RE 2 - H373 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.025 EFSA 2010  
ARfD 0.1 EFSA 2010  
AOEL 0.015 EFSA 2010  
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