NDC11 49035000444
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 |
|---|---|
| 49035-0004-44 | 49035-0004 |
| 49035-004-44 | 49035-004 |
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 |
|---|---|---|---|---|---|---|
| Anticavity Rinse | SODIUM FLUORIDE | Walmart Inc. | 3beb65e4-ae8e-4e51-b9ba-181cbec41eff | 2026-02-27 | Warnings, Adverse reactions | 49035-004-44 49035-004 49035000444 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.