Dr Lift Mineral SPF 30
- Product NDC
- 68062-8312
- 11-digit product format
- 680628312
- Labeler code
- 68062
- Product ID
- 68062-8312_40c0e413-70f6-25c9-e063-6294a90ad27d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- titanium dioxide
- Dosage form
- SPRAY
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-09
- Substance
- TITANIUM DIOXIDE
- Active strength
- 72 mg/100mL
- 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 Mineral SPF 30
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TITANIUM DIOXIDE | 72 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 15FIX9V2JP |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-8312-1 | Dr Lift Mineral SPF 30 | 100 mL in 1 BOTTLE, SPRAY | SPRAY | 100 | | 1 |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-8312-1 | 68062831201 | 100 mL in 1 BOTTLE, SPRAY (68062-8312-1) | 100 ml | 2025-10-09 | No | No | Current |