NDC11 55873000101
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 |
|---|---|
| 55873-0001-01 | 55873-0001 |
| 55873-0001-1 | 55873-0001 |
| 55873-001-01 | 55873-001 |
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 |
|---|---|---|---|---|---|---|
| OralLine Secure | SODIUM FLUORIDE | J.M. Murray Center Inc. | 4c0970e9-7417-4234-89e3-3b602a609af5 | 2025-03-20 | Warnings | 55873-001-01 55873-001 55873000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.