NDC11 10237063045
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 |
|---|---|
| 10237-0630-45 | 10237-0630 |
| 10237-630-45 | 10237-630 |
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 |
|---|---|---|---|---|---|---|
| AIM Cavity Protection with Whitening | SODIUM FLUORIDE | Church & Dwight Co., Inc. | a8c742e1-ee61-4593-b8f5-b9e586d39dfc | 2026-07-01 | Warnings | 10237-630-45 10237-630 10237063045 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.