NDC11 24208053775
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 |
|---|---|
| 24208-0537-75 | 24208-0537 |
| 24208-537-75 | 24208-537 |
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 |
|---|---|---|---|---|---|---|
| LUMIFY Redness Reliever Eye Drops | BRIMONIDINE TARTRATE | Bausch & Lomb Incorporated | 022de945-0b26-40ae-8e88-d3fe2464d106 | 2026-03-31 | Warnings | 24208-537-75 24208-537 24208053775 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.