NDC11 87786005201
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 |
|---|---|
| 87786-0052-01 | 87786-0052 |
| 87786-0052-1 | 87786-0052 |
| 87786-052-01 | 87786-052 |
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 |
|---|---|---|---|---|---|---|
| Orraya WART REMOVER Liquid | SALICYLIC ACID 40% WART REMOVER LIQUID | Wenzhou Yuyuan Pharmaceutical Co., Ltd. | 5a2cf1de-789c-04b0-e063-6394a90ac59e | 2026-08-29 | Warnings | 87786-052-01 87786-052 87786005201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.