NDC11 76162035332
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 |
|---|---|
| 76162-0353-32 | 76162-0353 |
| 76162-353-32 | 76162-353 |
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 |
|---|---|---|---|---|---|---|
| Dandruff | PYRITHIONE ZINC | Topco Associates LLC | a0f2c58b-bb17-42a3-bd90-be771f60ef20 | 2026-02-13 | Warnings, Adverse reactions | 76162-353-32 76162-353 76162035332 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.