NDC11 66975077901
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 |
|---|---|
| 66975-0779-01 | 66975-0779 |
| 66975-0779-1 | 66975-0779 |
| 66975-779-01 | 66975-779 |
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 |
|---|---|---|---|---|---|---|
| PRO-SYS | PROFESSIONAL SENSITIVITY, SLS FREE - MINT (5000 PPM) | Benco Dental | 4e4761d7-f1ab-aae4-e063-6294a90a214c | 2025-12-01 | Warnings | 66975-779-01 66975-779 66975077901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.