NDC11 63615000101
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 |
|---|---|
| 63615-0001-01 | 63615-0001 |
| 63615-0001-1 | 63615-0001 |
| 63615-001-01 | 63615-001 |
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 |
|---|---|---|---|---|---|---|
| Cavity Protection Fresh Mint Anticavity Mouthwash | SODIUM FLUORIDE | Oxyfresh Worldwide Inc | 3efc66b2-fcf9-4d26-9cdd-1af8225312b4 | 2025-09-10 | Warnings | 63615-001-01 63615-001 63615000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.