ANTIBACTERIAL HANDWASH
- Product NDC
- 52000-041
- 11-digit product format
- 520000041
- Labeler code
- 52000
- Product ID
- 52000-041_109449ee-1540-4094-a346-36d724d5ef9e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- benzalkonium chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- Universal Distribution Center LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2018-08-01
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .13 g/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ANTIBACTERIAL HANDWASH
- Brand name suffix
- PEACH DREAM
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | .13 g/100mL |
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 |
|---|
| 52000-041-01 | ANTIBACTERIAL HANDWASHPEACH DREAM | 400 mL in 1 BOTTLE | LIQUID | 400 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52000-041 | ANTIBACTERIAL HANDWASH PEACH DREAM (BENZALKONIUM CHLORIDE) LIQUID [UNIVERSAL DISTRIBUTION CENTER LLC] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241212_7479686e-10f1-49e0-e053-2a91aa0ae882.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52000-041-01 | 52000004101 | 400 mL in 1 BOTTLE (52000-041-01) | 400 ml | 2018-08-01 | 0000-00-00 | No | No | Current |