NDC11 84126060803
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 |
|---|---|
| 84126-0608-03 | 84126-0608 |
| 84126-0608-3 | 84126-0608 |
| 84126-608-03 | 84126-608 |
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 Pro-Health Maximum Cavity Protection | STANNOUS FLUORIDE | The Procter & Gamble Manufacturing Company | 2eaeddc5-1559-9378-e063-6394a90a4ed7 | 2026-01-08 | Warnings | 84126-608-03 84126-608 84126060803 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.