Dr Lift Sun Care SPF 25
- Product NDC
- 68062-8821
- 11-digit product format
- 680628821
- Labeler code
- 68062
- Product ID
- 68062-8821_48dfdb53-adeb-1fd4-e063-6394a90a51dc
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- titanium dioxide, zinc oxide
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M020
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-03-21
- Substance
- AVOBENZONE; HOMOSALATE; OCTISALATE
- Active strength
- 1.35; 6.75; 2.25 mg/45mL; mg/45mL; mg/45mL
- 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 Sun Care SPF 25
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AVOBENZONE | 1.35 mg/45mL |
| HOMOSALATE | 6.75 mg/45mL |
| OCTISALATE | 2.25 mg/45mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | G63QQF2NOX, V06SV4M95S, 4X49Y0596W |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-8821-1 | Dr Lift Sun Care SPF 25 | 25 mL in 1 BOTTLE, PUMP | LOTION | 25 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-8821 | DR LIFT SUN CARE SPF 25 (TITANIUM DIOXIDE, ZINC OXIDE) LOTION [SPA DE SOLEIL] | 1 | Current NDC, 1 package rows | 20230322_f76e616c-e119-b509-e053-6294a90a2508.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-8821-1 | 68062882101 | 25 mL in 1 BOTTLE, PUMP (68062-8821-1) | 25 ml | 2023-03-21 | No | No | Current |