NDC11 41163001145
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 |
|---|---|
| 41163-0011-45 | 41163-0011 |
| 41163-011-45 | 41163-011 |
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 | SODIUM FLUORIDE | United Natural Foods, Inc. dba UNFI | dd6bf8df-1e28-4f61-b876-b9f1f8d5993a | 2026-02-17 | Warnings, Adverse reactions | 41163-011-45 41163-011 41163001145 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.