NDC11 51326090008
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 |
|---|---|
| 51326-0900-08 | 51326-0900 |
| 51326-0900-8 | 51326-0900 |
| 51326-900-08 | 51326-900 |
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 |
|---|---|---|---|---|---|---|
| Sanix Alcohol Hand Rub | ALCOHOL | Topiderm, Inc | a4fbb714-4f20-400a-ab98-f1c8807ce6fc | 2020-03-24 | Warnings | 51326-900-08 51326-900 51326090008 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.