NDC11 69510001019
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 |
|---|---|
| 69510-0010-19 | 69510-0010 |
| 69510-010-19 | 69510-010 |
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 |
|---|---|---|---|---|---|---|
| Ipana Wintergreen Fluoride | SODIUM MONOFLUOROPHOSPHATE | Maxill Inc. | 5776cc3e-4fd1-4bd7-8d82-f82508e6b8d0 | 2025-07-28 | Warnings | 69510-010-19 69510-010 69510001019 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.