NDC11 70708089016
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 |
|---|---|
| 70708-0890-16 | 70708-0890 |
| 70708-890-16 | 70708-890 |
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 |
|---|---|---|---|---|---|---|
| GuruNanda Anti-Cavity | SODIUM FLUORIDE | GURUNANDA, LLC | 3b07b72f-4efc-eb0f-e063-6294a90a70a8 | 2026-01-19 | Warnings | 70708-890-16 70708-890 70708089016 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.