Dr Lift SPF 50 Mineral Sunscreen Stick
- Product NDC
- 68062-8314
- 11-digit product format
- 680628314
- Labeler code
- 68062
- Product ID
- 68062-8314_436fdf4f-11da-7c5b-e063-6294a90a8731
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Zinc Oxide
- Dosage form
- STICK
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-11-12
- Substance
- ZINC OXIDE
- Active strength
- 3.75 g/15g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr Lift SPF 50 Mineral Sunscreen Stick
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ZINC OXIDE | 3.75 g/15g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | SOI2LOH54Z |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-8314-1 | Dr Lift SPF 50 Mineral Sunscreen Stick | 15 g in 1 TUBE | STICK | 15 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-8314-1 | 68062831401 | 15 g in 1 TUBE (68062-8314-1) | 15 g | 2025-11-12 | No | No | Current |