NDC11 10237026801
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 |
|---|---|
| 10237-0268-01 | 10237-0268 |
| 10237-0268-1 | 10237-0268 |
| 10237-268-01 | 10237-268 |
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 |
|---|---|---|---|---|---|---|
| TheraBreath AM-PM Twin Pack | SODIUM FLUORIDE | Church & Dwight Co., Inc. | 4618e390-9039-a1d0-e063-6294a90ab294 | 2025-12-16 | Warnings | 10237-268-01 10237-268 10237026801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.