NDC11 87204016601
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 |
|---|---|
| 87204-0166-01 | 87204-0166 |
| 87204-0166-1 | 87204-0166 |
| 87204-166-01 | 87204-166 |
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 |
|---|---|---|---|---|---|---|
| Flyleaf WART REMOVER | SALICYLIC ACID 20% | Guangzhou Huixue Biotechnology Co., Ltd. | 4a29e0f1-0ff3-f782-e063-6294a90a01ea | 2026-02-06 | Warnings | 87204-166-01 87204-166 87204016601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.