NDC11 74680010812
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 |
|---|---|
| 74680-0108-12 | 74680-0108 |
| 74680-108-12 | 74680-108 |
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 |
|---|---|---|---|---|---|---|
| Germ-Away | ANTIBACTERIAL HAND WIPE | Unico International Trading Corp | ad7d8546-d440-e661-e053-2a95a90a8fd3 | 2026-01-08 | Warnings | 74680-108-12 74680-108 74680010812 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.