NDC11 83781001301
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 |
|---|---|
| 83781-0013-01 | 83781-0013 |
| 83781-0013-1 | 83781-0013 |
| 83781-013-01 | 83781-013 |
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 |
|---|---|---|---|---|---|---|
| MQXUNMI BEE VENOM CORN CALLUS REMOVERS | BEE VENOM CORN CALLUS REMOVERS | Zhengzhou Miaoqi Medical Technology Co., Ltd. | 41952a0e-2bd2-db3c-e063-6294a90a4a79 | 2025-10-20 | Warnings | 83781-013-01 83781-013 83781001301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.