NDC11 69423093301
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 |
|---|---|
| 69423-0933-01 | 69423-0933 |
| 69423-0933-1 | 69423-0933 |
| 69423-933-01 | 69423-933 |
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 Whitening plus Scope | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | c5d5bc17-e81b-34aa-e053-2a95a90ad77f | 2026-01-08 | Warnings | 69423-933-01 69423-933 69423093301 |
| Toothpaste, plus Toothbrush | SODIUM FLUORIDE PASTE, DENTIFRICE AND TOOTHBRUSH | Lil' Drug Store Products, Inc. | 15ac00f8-da51-6cea-e063-6294a90aeb81 | 2024-04-09 | Warnings | 69423-933-01 69423093301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.