| Product NDC: | 66908-107 | 
| Proprietary Name: | ProFormance Series Foam Alcohol Hand Sanitizer | 
| Non Proprietary Name: | Ethyl Alcohol | 
| Active Ingredient(s): | 72 mL/100mL & nbsp; Ethyl Alcohol | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | LIQUID | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 66908-107 | 
| Labeler Name: | Pro-Link, Inc. | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333E | 
| Marketing Category: | OTC MONOGRAPH NOT FINAL | 
| Start Marketing Date: | 20110101 | 
| Package NDC: | 66908-107-27 | 
| Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (66908-107-27) | 
| NDC Code | 66908-107-27 | 
| Proprietary Name | ProFormance Series Foam Alcohol Hand Sanitizer | 
| Package Description | 1000 mL in 1 BOTTLE, PLASTIC (66908-107-27) | 
| Product NDC | 66908-107 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Ethyl Alcohol | 
| Dosage Form Name | LIQUID | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20110101 | 
| Marketing Category Name | OTC MONOGRAPH NOT FINAL | 
| Labeler Name | Pro-Link, Inc. | 
| Substance Name | ALCOHOL | 
| Strength Number | 72 | 
| Strength Unit | mL/100mL | 
| Pharmaceutical Classes |