Dr Lift Blemish
- Product NDC
- 68062-2265
- 11-digit product format
- 680622265
- Labeler code
- 68062
- Product ID
- 68062-2265_48dfd489-9f9b-ff51-e063-6294a90a25b0
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- salicylic acid
- Dosage form
- LOTION
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M006
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-06-27
- Substance
- SALICYLIC ACID; SULFUR
- Active strength
- 1; 2 mg/100mL; mg/100mL
- 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 Blemish
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SALICYLIC ACID | 1 mg/100mL |
| SULFUR | 2 mg/100mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | O414PZ4LPZ, 70FD1KFU70 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-2265-1 | Dr Lift Blemish | 100 mL in 1 BOTTLE | LOTION | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-2265 | DR LIFT BLEMISH (SALICYLIC ACID) LOTION [SPA DE SOLEIL] | 1 | Current NDC, 1 package rows | 20230629_ff2974d3-39e0-0fcc-e053-6294a90a0f3e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68062-2265-1 | 68062226501 | 100 mL in 1 BOTTLE (68062-2265-1) | 100 ml | 2023-06-27 | No | No | Current |