NDC11 21130035120
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 |
|---|---|
| 21130-0351-20 | 21130-0351 |
| 21130-351-20 | 21130-351 |
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 |
|---|---|---|---|---|---|---|
| Signature Care Sensitive Maximum Strength | POTASSIUM NITRATE, SODIUM FLUORIDE | Safeway | 83225fe5-0490-eb4b-e053-2a91aa0a6879 | 2025-11-14 | Warnings | 21130-351-20 21130-351 21130035120 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.