NDC11 35000095371
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 |
|---|---|
| 35000-0953-71 | 35000-0953 |
| 35000-953-71 | 35000-953 |
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 |
|---|---|---|---|---|---|---|
| Colgate Cavity Protection | SODIUM FLUORIDE | Colgate-Palmolive Company | cdd2ad04-8c65-40f2-b323-5ce11af52e4f | 2026-07-06 | Warnings | 35000-953-71 35000-953 35000095371 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.