NDC11 85636000301
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 |
|---|---|
| 85636-0003-01 | 85636-0003 |
| 85636-0003-1 | 85636-0003 |
| 85636-003-01 | 85636-003 |
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 Patch | WART REMOVER PATCH | Shenzhen Earth Surface Trading Co., Ltd. | 37bcc410-baa4-1735-e063-6394a90acf8d | 2025-06-16 | Warnings | 85636-003-01 85636-003 85636000301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.