NDC11 69423084850
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 |
|---|---|
| 69423-0848-50 | 69423-0848 |
| 69423-848-50 | 69423-848 |
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 |
|---|---|---|---|---|---|---|
| Crest Pro-Health Advanced Anti-Cavity Max Cavity | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 15d70b80-3b25-bc32-e063-6394a90a163e | 2026-01-08 | Warnings | 69423-848-50 69423-848 69423084850 |