NDC11 00363205302
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 00363-2053-02 | 00363-2053 |
| 00363-2053-2 | 00363-2053 |
| 0363-2053-02 | 0363-2053 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Walgreens Pain Burn Itch Relief | BENZOCAINE 20%, MENTHOL 0.5% | Walgreens | cc6e4b42-fdd8-6ff7-e053-2995a90a3d1d | 2024-12-11 | Warnings | 0363-2053-02 0363-2053 00363205302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.