NDC 74690-024 - Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 74690-024
- Package NDCs from labels
- 74690-024-00
- Manufacturer
- Farmasi US LLC
- Effective date
- 2023-11-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF - Farmasi US LLC | Farmasi US LLC | 2023-11-05 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 74690-024-00 | Dr. C. Tuna Lumi Radiance Brightening Cream 22 SPF | 2.5 mL in 1 PACKET | CREAM | 2.5 mL | 60 mg in 1mL | 2 |
DailyMed Dashboard NDC Coverage#
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.
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| Hemorrhoidal | LIDOCAINE, MINERAL OIL, PHENYLEPHRINE HCL, WHITE PETROLATUM | Walgreens Co | 3d213ba8-3cbe-11c4-e063-6394a90ae016 | 2026-03-30 | Warnings | T5L8T28FGP |
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| ULTRALIGHT AGE DEFENSE SPF 50 | ZINC OXIDE | Guangzhou Origin Beauty Cosmetics Co., Ltd. | 4e36a743-7906-2b7b-e063-6294a90af314 | 2026-03-29 | Warnings | M020 |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.