NDC11 84126066423
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 |
|---|---|
| 84126-0664-23 | 84126-0664 |
| 84126-664-23 | 84126-664 |
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 Plus Scope plus Whitening Outlast Mint | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 5513ba92-cadc-2cf3-e063-6294a90ac3e5 | 2026-06-25 | Warnings | 84126-664-23 84126-664 84126066423 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.