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Please be aware that this old REACH registration data factsheet is no longer maintained; it remains frozen as of 19th May 2023.

The new ECHA CHEM database has been released by ECHA, and it now contains all REACH registration data. There are more details on the transition of ECHA's published data to ECHA CHEM here.

Diss Factsheets

Toxicological information

Eye irritation

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Administrative data

Endpoint:
eye irritation: in vivo
Type of information:
experimental study
Adequacy of study:
weight of evidence
Reliability:
2 (reliable with restrictions)
Rationale for reliability incl. deficiencies:
guideline study without detailed documentation

Data source

Reference
Reference Type:
other company data
Title:
Unnamed
Year:
1986

Materials and methods

Test guideline
Qualifier:
according to guideline
Guideline:
OECD Guideline 405 (Acute Eye Irritation / Corrosion)
GLP compliance:
not specified

Test material

Constituent 1
Reference substance name:
Fluorescent Brightener 121
IUPAC Name:
Fluorescent Brightener 121

Test animals / tissue source

Species:
rabbit
Strain:
New Zealand White

Test system

Vehicle:
unchanged (no vehicle)
Amount / concentration applied:
0.1 ml/eye

Results and discussion

In vivo

Resultsopen allclose all
Irritation parameter:
cornea opacity score
Basis:
animal: not available
Time point:
24/48/72 h
Remarks on result:
other: not irritating
Irritation parameter:
iris score
Basis:
animal: not available
Time point:
24/48/72 h
Remarks on result:
other: not irritating
Irritation parameter:
conjunctivae score
Basis:
animal: not available
Time point:
24/48/72 h
Remarks on result:
other: not irritating
Irritation parameter:
chemosis score
Basis:
animal: not available
Time point:
24/48/72 h
Remarks on result:
other: not irritating
Irritant / corrosive response data:
no additional details available

Applicant's summary and conclusion

Conclusions:
Not irritating
Executive summary:

The eye irritation potential of test item was investigated in New Zealand rabbits; the study was conducted according to the OECD guideline 405. Test item was administrated undiluted, 0.1 ml per eye. The substance was indicated to be not eye irritating.

Conclusion

Not irritating