NDC11 66923000343
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 |
|---|---|
| 66923-0003-43 | 66923-0003 |
| 66923-003-43 | 66923-003 |
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 | e91ed8a1-0d45-402c-9c16-1ae72e695a37 | 2024-11-20 | Warnings | 66923-003-43 66923-003 66923000343 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.