NDC11 21749071304
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 |
|---|---|
| 21749-0713-04 | 21749-0713 |
| 21749-0713-4 | 21749-0713 |
| 21749-713-04 | 21749-713 |
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 |
|---|---|---|---|---|---|---|
| Purell Advanced Soothing | ALCOHOL | GOJO Industries, LLC | 59b47629-8b4e-4084-8bc8-66c7e5599e9c | 2026-07-10 | Warnings | 21749-713-04 21749-713 21749071304 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.