NDC11 83818000701
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 |
|---|---|
| 83818-0007-01 | 83818-0007 |
| 83818-0007-1 | 83818-0007 |
| 83818-007-01 | 83818-007 |
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 Milia Remover 30 ml | MILIA REMOVER | Shenzhen Xinxin Yunhai Technology Co., Ltd. | 27b78b20-5c65-10ad-e063-6394a90ad22e | 2024-11-25 | Warnings | 83818-007-01 83818-007 83818000701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.