Zest Antibacterial Liquid Hand Soap, Fresh Aqua
- Product NDC
- 81277-013
- 11-digit product format
- 812770013
- Labeler code
- 81277
- Product ID
- 81277-013_2e7120ac-b045-7cbb-e063-6294a90a19b3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- BENZALKONIUM CHLORIDE
- Dosage form
- GEL
- Route
- TOPICAL
- Labeler
- Sodalis USA, LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-07-15
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 1.3 mg/mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Zest Antibacterial Liquid Hand Soap, Fresh Aqua
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 1.3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F5UM2KM3W7 |
| Rxcui | 1046593 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 81277-013-01 | Zest Antibacterial Liquid Hand Soap, Fresh Aqua | 221 mL in 1 BOTTLE, PUMP | GEL | 221 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 81277-013 | ZEST ANTIBACTERIAL LIQUID HAND SOAP, FRESH AQUA (BENZALKONIUM CHLORIDE) GEL [SODALIS USA, LLC] | 1 | Current NDC, 1 package rows | 20250221_72ca863e-9872-45a5-b30d-e615339970d8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 81277-013-01 | 81277001301 | 221 mL in 1 BOTTLE, PUMP (81277-013-01) | 221 ml | 2020-07-15 | No | No | Current |