NDC11 66923000700
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 |
|---|---|
| 66923-0007-0 | 66923-0007 |
| 66923-0007-00 | 66923-0007 |
| 66923-007-00 | 66923-007 |
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 |
|---|---|---|---|---|---|---|
| Firefly Anticavity Fluoride | SODIUM FLUORIDE | Ranir LLC | 9f98913f-6754-4e1c-98cf-b89fe87750f8 | 2024-11-25 | Warnings | 66923-007-00 66923-007 66923000700 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.