NDC11 76670001602
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 |
|---|---|
| 76670-0016-02 | 76670-0016 |
| 76670-0016-2 | 76670-0016 |
| 76670-016-02 | 76670-016 |
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 |
|---|---|---|---|---|---|---|
| DOCTRUST ONE S Tooth | SODIUM FLUORIDE, DENTAL TYPE SILICA, POTASSIUM NIRATE | DOCSMEDI Co., Ltd. | 3382776a-a10e-1823-e063-6394a90a6f91 | 2025-04-24 | Warnings | 76670-0016-2 76670-0016 76670001602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.