NDC11 30142048286
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 |
|---|---|
| 30142-0482-86 | 30142-0482 |
| 30142-482-86 | 30142-482 |
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 |
|---|---|---|---|---|---|---|
| Alcohol-Free Anticavity | SODIUM FLUORIDE | The Kroger Co. | 5459eeee-adf0-4afe-b190-62d4fa113806 | 2026-02-27 | Warnings, Adverse reactions | 30142-482-86 30142-482 30142048286 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.