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 | M017 | openfda.application_number | |
| brand name | Itch Relief Gel | openfda.brand_name | |
| generic name | ITCH RELIEF GEL | openfda.generic_name | |
| manufacturer name | Pharma Nobis, LLC | openfda.manufacturer_name | |
| ndc | package | 82645-901-94 | openfda.package_ndc |
| ndc | product | 82645-901 | openfda.product_ndc |
| ndc11 | package | 82645090194 | derived:openfda.package_ndc |
| spl id | 0d1cd578-e127-6e8e-e063-6294a90a5060 | id | |
| spl set id | e42f484d-a641-3489-e053-2a95a90a4254 | set_id | |
| unii | TC2D6JAD40 | 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.