NDC11 79481020101
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 |
|---|---|
| 79481-0201-01 | 79481-0201 |
| 79481-0201-1 | 79481-0201 |
| 79481-201-01 | 79481-201 |
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 | Meijer, Inc. | b17f7a5d-272e-446d-803b-46a6d8e5f18f | 2026-02-19 | Warnings, Adverse reactions | 79481-0201-1 79481-0201 79481020101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.