NDC11 73656001900
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 |
|---|---|
| 73656-0019-0 | 73656-0019 |
| 73656-0019-00 | 73656-0019 |
| 73656-019-00 | 73656-019 |
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 |
|---|---|---|---|---|---|---|
| White Glo Professional White AntiCavity | SODIUM MONOFLUOROPHOSPHATE | WHITE GLO USA INC | 1fb04108-31b3-43dd-9509-bfa846113516 | 2025-02-26 | Warnings | 73656-019-00 73656-019 73656001900 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.