NDC11 87298005301
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 |
|---|---|
| 87298-0053-01 | 87298-0053 |
| 87298-0053-1 | 87298-0053 |
| 87298-053-01 | 87298-053 |
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. | 594ecfe5-8d9d-be3b-e063-6294a90a5f2e | 2026-08-18 | Warnings | 87298-053-01 87298-053 87298005301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.