NDC11 74690000301
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 |
|---|---|
| 74690-0003-01 | 74690-0003 |
| 74690-0003-1 | 74690-0003 |
| 74690-003-01 | 74690-003 |
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 |
|---|---|---|---|---|---|---|
| Dr. C. Tuna Lumi Radiance Brightening | OCTOCRYLENE, OCTINOXATE, AVOBENZONE | Farmasi US LLC | adf5621b-7cf0-53b3-e053-2a95a90a8058 | 2026-01-09 | Warnings | 74690-003-01 74690-003 74690000301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.