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 |
|---|
| CUTANEOUS |
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 | M016 | openfda.application_number | |
| brand name | Aluroderm Scar | openfda.brand_name | |
| generic name | ALLANTOIN | openfda.generic_name | |
| manufacturer name | Asclemed USA, Inc. | openfda.manufacturer_name | |
| ndc | package | 76420-955-01 | openfda.package_ndc |
| ndc | product | 76420-955 | openfda.product_ndc |
| ndc11 | package | 76420095501 | derived:openfda.package_ndc |
| rxcui | 2711688 | openfda.rxcui | |
| spl id | 31b18752-52bd-1354-e063-6394a90a31f1 | id | |
| spl set id | 60656ca1-5218-4595-854e-19f1061def1e | set_id | |
| unii | 344S277G0Z | 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.