NDC11 73928007902
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 |
|---|---|
| 73928-0079-02 | 73928-0079 |
| 73928-0079-2 | 73928-0079 |
| 73928-079-02 | 73928-079 |
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 |
|---|---|---|---|---|---|---|
| HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 38c323e2-9a9a-f898-e063-6394a90aa226 | 2025-06-30 | Warnings | 73928-079 |
| HAND SANITIZER | ALCOHOL ANTISEPTIC | Kingkey MBC Life Technology Group Co.,Ltd | 38b87b19-7663-d5c5-e063-6294a90a9e87 | 2025-06-29 | Warnings | 73928-079-02 73928-079 73928007902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.