NDC11 37808057686
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 |
|---|---|
| 37808-0576-86 | 37808-0576 |
| 37808-576-86 | 37808-576 |
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 |
|---|---|---|---|---|---|---|
| Alcohol Free Refreshing Mint | SODIUM FLUORIDE | H E B | cedf7c08-7412-4733-9b67-225b331cec8c | 2026-04-27 | Warnings, Adverse reactions | 37808-576-86 37808-576 37808057686 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.