 
                        | Product NDC: | 63998-575 | 
| Proprietary Name: | MicroMousse II Alcohol Free Hand Sanitizing Foam | 
| Non Proprietary Name: | BENZETHONIUM CHLORIDE | 
| Active Ingredient(s): | 2 mg/mL & nbsp; BENZETHONIUM CHLORIDE | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63998-575 | 
| Labeler Name: | United Laboratories, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333 | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20091130 | 
| Package NDC: | 63998-575-14 | 
| Package Description: | 3785 mL in 1 BOTTLE, PLASTIC (63998-575-14) | 
| NDC Code | 63998-575-14 | 
| Proprietary Name | MicroMousse II Alcohol Free Hand Sanitizing Foam | 
| Package Description | 3785 mL in 1 BOTTLE, PLASTIC (63998-575-14) | 
| Product NDC | 63998-575 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | BENZETHONIUM CHLORIDE | 
| Dosage Form Name | LIQUID | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20091130 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | United Laboratories, Inc. | 
| Substance Name | BENZETHONIUM CHLORIDE | 
| Strength Number | 2 | 
| Strength Unit | mg/mL | 
| Pharmaceutical Classes |