NDC11 85601007002
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 |
|---|---|
| 85601-0070-02 | 85601-0070 |
| 85601-0070-2 | 85601-0070 |
| 85601-070-02 | 85601-070 |
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 |
|---|---|---|---|---|---|---|
| DENTI BUONGIORNO GUM CARE TOOTH | SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE | ATOSAFE CO., Ltd | 4115d122-3090-d3e5-e063-6294a90aafb6 | 2025-10-13 | Warnings | 85601-070-02 85601-070 85601007002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.