NDC11 79940001000
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 |
|---|---|
| 79940-0010-0 | 79940-0010 |
| 79940-0010-00 | 79940-0010 |
| 79940-010-00 | 79940-010 |
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 Anticavity | SODIUM MONOFLUOROPHOSPHATE | FORMIA LIMITED | b5eec445-d93a-4abb-a5e3-bfcde6fa2013 | 2026-01-28 | Warnings | 79940-010-00 79940-010 79940001000 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.