NDC11 79940001300
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 |
|---|---|
| 79940-0013-0 | 79940-0013 |
| 79940-0013-00 | 79940-0013 |
| 79940-013-00 | 79940-013 |
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 | 48ef2635-7157-4cd7-9f99-967f0143f7f1 | 2026-02-09 | Warnings | 79940-013-00 79940-013 79940001300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.