UP and UP
- Product NDC
- 82442-088
- 11-digit product format
- 824420088
- Labeler code
- 82442
- Product ID
- 82442-088_51531f24-f43f-f7d9-e063-6294a90a0394
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- TARGET CORPORATION INC.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-10-22
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- 130 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
- UP and UP
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BENZALKONIUM CHLORIDE | 130 mg/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 |
|---|
| 82442-088-07 | UP and UP | 222 mL in 1 BOTTLE, PLASTIC | LIQUID | 222 | | 5 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 82442-088-07 | 82442008807 | 222 mL in 1 BOTTLE, PLASTIC (82442-088-07) | 222 ml | 2025-10-22 | No | No | Historical |