NDC11 61578021302
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 |
|---|---|
| 61578-0213-02 | 61578-0213 |
| 61578-0213-2 | 61578-0213 |
| 61578-213-02 | 61578-213 |
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 |
|---|---|---|---|---|---|---|
| Gel 1100 Mint | SODIUM FLUORIDE | Dental Alliance Holdings LLC | f125fb04-5045-5367-e053-2a95a90aa73b | 2025-12-29 | Warnings | 61578-213-02 61578-213 61578021302 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.