NDC11 87204019101
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 |
|---|---|
| 87204-0191-01 | 87204-0191 |
| 87204-0191-1 | 87204-0191 |
| 87204-191-01 | 87204-191 |
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 |
|---|---|---|---|---|---|---|
| GPPEE WART REMOVER PATCHES | SALICYLIC ACID 40% | Guangzhou Huixue Biotechnology Co., Ltd. | 568a84eb-c0f7-6ce6-e063-6294a90a15b4 | 2026-09-08 | Warnings | 87204-191-01 87204-191 87204019101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.