PURELL Antimicrobial Foaming Hand
- Product NDC
- 21749-610
- 11-digit product format
- 217490610
- Labeler code
- 21749
- Product ID
- 21749-610_2a976ebe-2fd0-a496-e063-6294a90a2dae
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Benzalkonium Chloride
- Dosage form
- LIQUID
- Route
- TOPICAL
- Labeler
- GOJO Industries, Inc.
- Application
- 505G(a)(3)
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2023-12-11
- Substance
- BENZALKONIUM CHLORIDE
- Active strength
- .5 mg/100mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F5UM2KM3W7 | BENZALKONIUM CHLORIDE | 8001-54-5 | BENZALKONIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 21749-610-40 | 21749061040 | 1200 mL in 1 PACKAGE (21749-610-40) | 1200 ml | 2023-12-11 | No | No | Historical |