NDC11 85636003001
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 |
|---|---|
| 85636-0030-01 | 85636-0030 |
| 85636-0030-1 | 85636-0030 |
| 85636-030-01 | 85636-030 |
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 |
|---|---|---|---|---|---|---|
| Skin Wart Remover Liquid | SKIN WART REMOVER LIQUID | Shenzhen Earth Surface Trading Co., Ltd. | 5888ba63-1948-f6e6-e063-6394a90a0414 | 2026-08-08 | Warnings | 85636-030-01 85636-030 85636003001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.