NDC11 41250016386
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 |
|---|---|
| 41250-0163-86 | 41250-0163 |
| 41250-163-86 | 41250-163 |
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 | Meijer, Inc. | c628d02f-c834-42b3-b38d-6b9cdcdd0961 | 2026-02-19 | Warnings, Adverse reactions | 41250-163-86 41250-163 41250016386 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.