Dr Lift Antibacterial Hand Wash
- Product NDC
- 68062-2242
- 11-digit product format
- 680622242
- Labeler code
- 68062
- Product ID
- 68062-2242_50b719c9-4516-85fd-e063-6294a90a9103
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Spa de Soleil
- Application
- M003
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-29
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .46 mg/240mg
- 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 Antibacterial Hand Wash
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .46 mg/240mg |
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 |
|---|
| 68062-2242-1 | Dr Lift Antibacterial Hand Wash | 240 mg in 1 TUBE | GEL | 240 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68062-2242 | DR LIFT ANTIBACTERIAL HAND WASH (BENZALKONIUM CHLORIDE) GEL [SPA DE SOLEIL] | 1 | Current NDC, Legacy NDC, 1 package rows | 20200730_ab9e2c3c-d422-255e-e053-2a95a90a7a22.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68062-2242-1 | 68062224201 | 240 mg in 1 TUBE (68062-2242-1) | 240 mg | 2020-07-29 | 0000-00-00 | No | No | Current |