NDC11 00126008802
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 |
|---|---|
| 00126-0088-02 | 00126-0088 |
| 00126-0088-2 | 00126-0088 |
| 00126-088-02 | 00126-088 |
| 0126-0088-02 | 0126-0088 |
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 |
|---|---|---|---|---|---|---|
| PreviDent Fresh Mint | SODIUM FLUORIDE | Colgate Oral Pharmaceuticals, Inc. | 2ecc57ec-cd25-4911-9247-6375569b8abe | 2023-03-17 | Warnings, Adverse reactions | 0126-0088-02 0126-0088 00126008802 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.