Dr Lift Advanced Antibacterial Wipes
- Product NDC
- 68062-2244
- 11-digit product format
- 680622244
- Labeler code
- 68062
- Product ID
- 68062-2244_50b715dd-873e-7d39-e063-6294a90a861d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-17
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .156 mg/120mg
- 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 Advanced Antibacterial Wipes
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .156 mg/120mg |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68062-2244-1 | Dr Lift Advanced Antibacterial Wipes | 120 mg in 1 BOTTLE | LIQUID | 120 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-2244 | DR LIFT ADVANCED ANTIBACTERIAL WIPES (BENZALKONIUM CHLORIDE) LIQUID [SPA DE SOLEIL] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200918_af89bd25-784e-4828-e053-2995a90a8aaa.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68062-2244-1 | 68062224401 | 120 mg in 1 BOTTLE (68062-2244-1) | 120 mg | 2020-09-17 | 0000-00-00 | No | No | Current |