NDC11 00363055238
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 |
|---|---|
| 00363-0552-38 | 00363-0552 |
| 00363-552-38 | 00363-552 |
| 0363-0552-38 | 0363-0552 |
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 |
|---|---|---|---|---|---|---|
| Studio 35 External Analgesic Medicated Body | MENTHOL AND ZINC OXIDE | Walgreen Co | 2dd63063-45c1-4029-99ac-0962a27a5ddc | 2017-02-08 | Warnings | 0363-0552-38 0363-0552 00363055238 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.