warnings
WARNINGS For External use only
Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops
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
- Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops
- Generic name
- HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V
- Manufacturer
- Aurolab
- Product type
- HUMAN OTC DRUG
- SPL set ID
- f27a6799-e2f1-ee8d-e053-2a95a90aead1
- SPL ID
- 495bffb8-e350-e359-e063-6294a90a32c3
- Version
- 7
- Effective date
- 2026-01-27
- Source export date
- 2026-10-27
- Source partition
- 11
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/b7a5e61d87a3b8f87f4c3ff7b526bfbf6baf84c840f565574c7d83d4083e2b38/drug-label-0011-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:49:07
| 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 |
|---|---|---|---|
| application number | M018 | openfda.application_number | |
| brand name | Aurovisc Lubricant HYPROMELLOSE 2208 (15000 MPA.S) Gel/Drops | openfda.brand_name | |
| generic name | HYPROMELLOSE OPHTHALMIC SOLUTION 2% W/V | openfda.generic_name | |
| manufacturer name | Aurolab | openfda.manufacturer_name | |
| ndc | package | 16030-303-02 | openfda.package_ndc |
| ndc | product | 16030-303 | openfda.product_ndc |
| ndc11 | package | 16030030302 | derived:openfda.package_ndc |
| rxcui | 1147664 | openfda.rxcui | |
| spl id | 495bffb8-e350-e359-e063-6294a90a32c3 | id | |
| spl set id | f27a6799-e2f1-ee8d-e053-2a95a90aead1 | set_id | |
| unii | Z78RG6M2N2 | 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.