NDC11 69423091865
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 |
|---|---|
| 69423-0918-65 | 69423-0918 |
| 69423-918-65 | 69423-918 |
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 Complete Plus Scope Outlast Ultra | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | c3f63455-b09e-9877-e053-2a95a90a1844 | 2026-01-08 | Warnings | 69423-918-65 69423-918 69423091865 |