NDC11 49035097186
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 |
|---|---|
| 49035-0971-86 | 49035-0971 |
| 49035-971-86 | 49035-971 |
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 | Walmart Inc. | 4590ca97-130c-46b2-9ba0-38f4703ef30a | 2026-02-27 | Warnings, Adverse reactions | 49035-971-86 49035-971 49035097186 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.