NDC11 70683070302
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 |
|---|---|
| 70683-0703-02 | 70683-0703 |
| 70683-0703-2 | 70683-0703 |
| 70683-703-02 | 70683-703 |
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 |
|---|---|---|---|---|---|---|
| Dentisse | SODIUM FLUORIDE | Dentisse, Inc. | 326b290a-9bd2-468e-e054-00144ff8d46c | 2025-11-04 | Warnings | 70683-0703-2 70683-0703 70683070302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.