Registration Dossier

Administrative data

Endpoint:
acute toxicity: dermal
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
2 (reliable with restrictions)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1985

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
OECD Guideline 402 (Acute Dermal Toxicity)
Deviations:
not specified
GLP compliance:
no

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Details on test animals and environmental conditions:
10 animal/dose

Administration / exposure

Details on dermal exposure:
10 animal/dose, dosage (0,3500,5000,7500,1000mg/kg)

Results and discussion

Effect levels
Dose descriptor:
LD50
Effect level:
6 000 mg/kg bw

Applicant's summary and conclusion