NDC11 37808001302
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 |
|---|---|
| 37808-0013-02 | 37808-0013 |
| 37808-0013-2 | 37808-0013 |
| 37808-013-02 | 37808-013 |
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 |
|---|---|---|---|---|---|---|
| Athletes Foot Ultra | BUTENAFINE HYDROCHLORIDE | H E B | 0841f741-6409-4d93-a6a7-901808f77bcd | 2025-07-03 | Warnings | 37808-013-02 37808-013 37808001302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.