NDC11 83818001301
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 |
|---|---|
| 83818-0013-01 | 83818-0013 |
| 83818-0013-1 | 83818-0013 |
| 83818-013-01 | 83818-013 |
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 |
|---|---|---|---|---|---|---|
| MEOLY Skin Tag Remover | SKIN TAG REMOVER LIQUID | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 36a72a43-fdbf-fcc1-e063-6394a90a4dc8 | 2025-06-03 | Warnings | 83818-013-01 83818-013 83818001301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.