NDC11 87298005601
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 |
|---|---|
| 87298-0056-01 | 87298-0056 |
| 87298-0056-1 | 87298-0056 |
| 87298-056-01 | 87298-056 |
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 |
|---|---|---|---|---|---|---|
| WART REMOVER | SALICYLIC ACID | Guangzhou Hechuang Commercial Service Co.,Ltd. | 59df0688-5d06-1da4-e063-6394a90a799b | 2026-08-25 | Warnings | 87298-056-01 87298-056 87298005601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.