NDC11 84126061482
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 |
|---|---|
| 84126-0614-82 | 84126-0614 |
| 84126-614-82 | 84126-614 |
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 Pro Advanced Freshness | SODIUM FLUORIDE | The Procter & Gamble Manufacturing Company | 325c3ab2-aaa2-a06f-e063-6294a90abefb | 2026-01-08 | Warnings | 84126-614-82 84126-614 84126061482 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.