NDC11 68987001415
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 |
|---|---|
| 68987-0014-15 | 68987-0014 |
| 68987-014-15 | 68987-014 |
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 |
|---|---|---|---|---|---|---|
| PureLife APF | SODIUM FLUORIDE | PureLife Dental | 44b91f76-1b7a-40fc-9c80-e1c915b3d2ca | 2022-01-19 | Warnings | 68987-014-15 68987-014 68987001415 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.