NDC11 10237026521
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 |
|---|---|
| 10237-0265-21 | 10237-0265 |
| 10237-265-21 | 10237-265 |
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 Anticavity | SODIUM FLUORIDE | Church & Dwight Co., Inc. | 3c5d58f1-ea8c-4708-bbc6-21e1cd1446da | 2025-09-19 | Warnings | 10237-265-21 10237-265 10237026521 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.