NDC11 70108025401
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 |
|---|---|
| 70108-0254-01 | 70108-0254 |
| 70108-0254-1 | 70108-0254 |
| 70108-254-01 | 70108-254 |
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 |
|---|---|---|---|---|---|---|
| evo SENSITIVE ANTI-CAVITY FLUORIDE SWEET MINT | POTASSIUM NITRATE, SODIUM FLUORIDE | Ashtel Studios, Inc. | bc74d2a6-fe34-44cf-b015-70ed4d47c933 | 2025-10-13 | Warnings | 70108-254-01 70108-254 70108025401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.