NDC11 85795000101
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 |
|---|---|
| 85795-0001-01 | 85795-0001 |
| 85795-0001-1 | 85795-0001 |
| 85795-001-01 | 85795-001 |
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 |
|---|---|---|---|---|---|---|
| BURRRER Wart Remover | WART REMOVER | Shenzhen TeLaFaErJiaLuo Technology Co., Ltd. | 374735f6-426d-8fe5-e063-6394a90ab2b8 | 2025-06-11 | Warnings | 85795-001-01 85795-001 85795000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.