warnings
Warnings For External Use Only
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
| Harmonized routes |
|---|
| TOPICAL |
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 | Hypromellose Eye Drops 0.7% | openfda.brand_name | |
| generic name | HYPROMELLOSE EYE DROPS 0.7% | openfda.generic_name | |
| manufacturer name | Aurolab | openfda.manufacturer_name | |
| ndc | package | 16030-101-10 | openfda.package_ndc |
| ndc | product | 16030-101 | openfda.product_ndc |
| ndc11 | package | 16030010110 | derived:openfda.package_ndc |
| spl id | 2ac6c72f-6f81-825c-e063-6294a90af661 | id | |
| spl set id | d35313d0-b190-5fb0-e053-2a95a90a5283 | set_id | |
| unii | RN3152OP35 | openfda.unii |
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse event summaries are temporarily unavailable. Other product information remains available.