NDC11 36800037609
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 |
|---|---|
| 36800-0376-09 | 36800-0376 |
| 36800-0376-9 | 36800-0376 |
| 36800-376-09 | 36800-376 |
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 |
|---|---|---|---|---|---|---|
| Salicylic Acid | WART REMOVER LIQUID | Topco Associates LLC | 78beaf1b-14a2-45f9-ad0d-0d8953d316b3 | 2025-10-07 | Warnings | 36800-376-09 36800-376 36800037609 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.