ProCure Foaming Antimicrobial Hand
- Product NDC
- 55681-042
- 11-digit product format
- 556810042
- Labeler code
- 55681
- Product ID
- 55681-042_3e002cee-6103-1db4-e063-6394a90ac7a1
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Hand Soap (Benzalkonium Chloride 0.13%)
- Dosage form
- SOAP
- Route
- TOPICAL
- Labeler
- Twin Med LLC
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2025-09-04
- 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
- ProCure Foaming Antimicrobial Hand
- 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 |
|---|
| 55681-042-10 | ProCure Foaming Antimicrobial Hand | 1000 mL in 1 CARTRIDGE | SOAP | 1000 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 55681-042-10 | 55681004210 | 1000 mL in 1 CARTRIDGE (55681-042-10) | 1000 ml | 2025-09-04 | No | No | Current |