Dr Lift SPF 50 Cream
- Product NDC
- 68062-9007
- 11-digit product format
- 680629007
- Labeler code
- 68062
- Product ID
- 68062-9007_48dfccec-6fcc-1369-e063-6394a90a3e0f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- titanium dioxide, zinc oxide
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-08-24
- Substance
- OCTINOXATE; ZINC OXIDE
- Active strength
- 3.75; 4.93 mg/50mL; mg/50mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Dr Lift SPF 50 Cream
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| OCTINOXATE | 3.75 mg/50mL |
| ZINC OXIDE | 4.93 mg/50mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 4Y5P7MUD51, SOI2LOH54Z |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-9007-1 | Dr Lift SPF 50 Cream | 50 mL in 1 TUBE | CREAM | 50 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-9007 | DR LIFT SPF 50 CREAM (TITANIUM DIOXIDE, ZINC OXIDE) CREAM [SPA DE SOLEIL] | 1 | Current NDC, 1 package rows | 20230829_0402c4ba-ff2a-cf25-e063-6294a90a776c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-9007-1 | 68062900701 | 50 mL in 1 TUBE (68062-9007-1) | 50 ml | 2023-08-24 | No | No | Current |