NDC11 36800000444
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 |
|---|---|
| 36800-0004-44 | 36800-0004 |
| 36800-004-44 | 36800-004 |
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 Fluoride Rinse | SODIUM FLUORIDE | Topco Associates LLC | 3b04142a-4a65-45ba-a5a2-e62b0c47ec55 | 2026-02-13 | Warnings, Adverse reactions | 36800-004-44 36800-004 36800000444 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.