Registration Dossier

Administrative data

Endpoint:
acute toxicity: oral
Type of information:
experimental study
Adequacy of study:
supporting study
Reliability:
1 (reliable without restriction)

Data source

Reference
Reference Type:
study report
Title:
Unnamed
Year:
1992

Materials and methods

Test guideline
Qualifier:
according to
Guideline:
OECD Guideline 401 (Acute Oral Toxicity)
Deviations:
not applicable
GLP compliance:
not specified
Test type:
acute toxic class method
Limit test:
yes

Test material

Reference
Name:
Unnamed
Type:
Constituent

Test animals

Species:
rat
Strain:
Sprague-Dawley
Sex:
male/female

Administration / exposure

Route of administration:
oral: unspecified
Vehicle:
water
Doses:
200 and 800 mg/Kg
No. of animals per sex per dose:
MALE 800 mg/Kg 5 ANIMALS 5 DEATHS
MALE 200 mg/Kg 5 AMINALS 0 DEATHS
FEMALE 200 mg/Kg 5 AMINALS 0 DEATHS
Control animals:
yes

Results and discussion

Preliminary study:
SEE ATTACH
Effect levels
Sex:
male
Dose descriptor:
LD50
Effect level:
> 200 - <= 2 000 mg/kg bw
Based on:
test mat.
Remarks:
SEE ATTACH FOR MORE INFORMATION
Remarks on result:
other: SEE ATTACH FOR MORE INFOMATION
Mortality:
SEX DOSE mg/Kg NUMBER ANIMALS NUMBER DEATHSÇ
M 800 5 5
M 200 5 0
F 200 5 0
Clinical signs:
SEE ATTACH
Body weight:
SEE ATTACH
Gross pathology:
SEE ATTACH

Applicant's summary and conclusion

Interpretation of results:
harmful
Remarks:
Migrated information Criteria used for interpretation of results: EU