warnings
WARNINGS: To avoid contamination do not touch tip of container to any surface. Replace cap after using. Not for use in conjunction with hot laser treatment. If solution changes color or becomes cloudy, do not use.
Goniotaire
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Goniotaire
- Generic name
- HYPROMELLOSE 2906 (4000 MPA.S)
- Manufacturer
- Altaire Pharmaceuticals Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 9ebedd36-523a-4f92-8fe9-33beaf7288f9
- SPL ID
- 3e98cefc-43d0-40bf-80be-651f17a39d4f
- Version
- 3
- Effective date
- 2022-10-28
- Source export date
- 2026-09-28
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 06:35:44
| Harmonized routes |
|---|
| OPHTHALMIC |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| brand name | Goniotaire | openfda.brand_name | |
| generic name | HYPROMELLOSE 2906 (4000 MPA.S) | openfda.generic_name | |
| manufacturer name | Altaire Pharmaceuticals Inc. | openfda.manufacturer_name | |
| ndc | package | 59390-182-13 | openfda.package_ndc |
| ndc | product | 59390-182 | openfda.product_ndc |
| ndc11 | package | 59390018213 | derived:openfda.package_ndc |
| rxcui | 310934 | openfda.rxcui | |
| spl id | 3e98cefc-43d0-40bf-80be-651f17a39d4f | id | |
| spl set id | 9ebedd36-523a-4f92-8fe9-33beaf7288f9 | set_id | |
| unii | 5EYA69XGAT | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.