NDC11 63404221001
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 |
|---|---|
| 63404-2210-01 | 63404-2210 |
| 63404-2210-1 | 63404-2210 |
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 |
|---|---|---|---|---|---|---|
| Sensitivity and Gum with Cavity Protection | POTASSIUM NITRATE AND SODIUM FLUORIDE | Health and Natural Beauty USA Corp | 137d6935-19a3-499d-957c-820156eec7a5 | 2026-05-22 | Warnings | 63404-2210-1 63404-2210 63404221001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.