Product NDC: | 66949-014 |
Proprietary Name: | Alcohol Foam San |
Non Proprietary Name: | Ethanol |
Active Ingredient(s): | 6.2 mL/10mL & nbsp; Ethanol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66949-014 |
Labeler Name: | Zep Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20080407 |
Package NDC: | 66949-014-01 |
Package Description: | 1000 mL in 1 BOTTLE, PLASTIC (66949-014-01) |
NDC Code | 66949-014-01 |
Proprietary Name | Alcohol Foam San |
Package Description | 1000 mL in 1 BOTTLE, PLASTIC (66949-014-01) |
Product NDC | 66949-014 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethanol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20080407 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Zep Inc. |
Substance Name | ALCOHOL |
Strength Number | 6.2 |
Strength Unit | mL/10mL |
Pharmaceutical Classes |