NDC11 84126066852
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 |
|---|---|
| 84126-0668-52 | 84126-0668 |
| 84126-668-52 | 84126-668 |
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 Premium Plus Scope Active Foam plus Whitening Minty Fresh | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 560815d6-018a-0c24-e063-6394a90a1071 | 2026-07-07 | Warnings | 84126-668-52 84126-668 84126066852 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.