NDC11 50814001801
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 |
|---|---|
| 50814-0018-01 | 50814-0018 |
| 50814-0018-1 | 50814-0018 |
| 50814-018-01 | 50814-018 |
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 |
|---|---|---|---|---|---|---|
| Refill 4 | ISOPROPYL ALCOHOL | GFA Production (Xiamen) Co., Ltd. | 51348666-53e3-4cc7-99ba-cf3f23ddbcf6 | 2025-01-27 | Warnings | 50814-018-01 50814-018 50814001801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.