NDC11 35000021495
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 |
|---|---|
| 35000-0214-95 | 35000-0214 |
| 35000-214-95 | 35000-214 |
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 MaxFresh Knockout | SODIUM FLUORIDE | Colgate-Palmolive Company | 0ffbb3a9-7bfa-4f6a-aef3-fde327a410c9 | 2026-09-09 | Warnings | 35000-214-95 35000-214 35000021495 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.