Registration Dossier

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
other information
Reliability:
1 (reliable without restriction)
Rationale for reliability incl. deficiencies:
other: GLP guideline study

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
2006

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
other: 92/69/EWG, B.3; OECD 402 (1992)
GLP compliance:
yes
Limit test:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
other: rat, Crl:CD(SD)

Administration / exposure

Type of coverage:
semiocclusive
Vehicle:
other: deionisiertes Wasser
Duration of exposure:
24 h

Results and discussion

Effect levels
Sex:
male/female
Dose descriptor:
LD50
Effect level:
> 5 000 mg/kg bw
Mortality:
Male: 5000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Female: 5000 mg/kg bw; Number of animals: 5; Number of deaths: 0
Clinical signs:
Signs of toxicity related to dose levels:
Systemische Toxizitäten oder Gewichtsverlust traten nicht
auf.
Gross pathology:
Effects on organs:
Es wurden keine Effekte beobachtet.
Other findings:
Signs of toxicity (local):
Es wurden keine Hautreaktionen beobachtet.

Todesfälle traten nicht auf.

Applicant's summary and conclusion

Interpretation of results:
not classified
Remarks:
Migrated information Criteria used for interpretation of results: EU