NDC11 61543175103
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 |
|---|---|
| 61543-1751-03 | 61543-1751 |
| 61543-1751-3 | 61543-1751 |
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 |
|---|---|---|---|---|---|---|
| Plus White | SODIUM MONOFLUOROPHOSPHATE | CCA Industries, Inc. | 7581b27b-6acb-45b0-8804-b5dae3498931 | 2018-08-01 | Warnings | 61543-1751-3 61543-1751 61543175103 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.