Luminous Sunscreen SPF 50
- Product NDC
- 84248-028
- 11-digit product format
- 842480028
- Labeler code
- 84248
- Product ID
- 84248-028_26e2b82c-8d7b-7261-e063-6394a90a7c0d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide, Titanium Dioxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- CLINICAL SKIN LLC
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2024-12-02
- Substance
- TITANIUM DIOXIDE; ZINC OXIDE
- Active strength
- 1.58; 22.4 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Luminous Sunscreen SPF 50
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 1.58 mg/1 |
| ZINC OXIDE | 22.4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP, SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 84248-028-01 | Luminous Sunscreen SPF 50 | 1 in 1 CARTON | CREAM | 1 | | 1 |
| 84248-028-01 | Luminous Sunscreen SPF 50 | 50 in 1 BOTTLE | CREAM | 50 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 84248-028-01 | 84248002801 | 1 BOTTLE in 1 CARTON (84248-028-01) / 50 CREAM in 1 BOTTLE | 1 bottle | 2024-12-02 | No | No | Current |