NDC11 50865071092
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 |
|---|---|
| 50865-0710-92 | 50865-0710 |
| 50865-710-92 | 50865-710 |
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 |
|---|---|---|---|---|---|---|
| Foaming Sanitizing Hand | ALCOHOL | Kutol Products Company | b2e22e51-88f5-4391-8705-3855c1645d80 | 2026-04-24 | Warnings | 50865-710-92 50865-710 50865071092 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.