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: | 66908-107-12 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (66908-107-12) |
NDC Code | 66908-107-12 |
Proprietary Name | ProFormance Series Foam Alcohol Hand Sanitizer |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (66908-107-12) |
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 |