Product NDC: | 66949-880 |
Proprietary Name: | Zep Foam San |
Non Proprietary Name: | Benzethonium Chloride |
Active Ingredient(s): | .02 g/10mL & nbsp; Benzethonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66949-880 |
Labeler Name: | Zep Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20030318 |
Package NDC: | 66949-880-12 |
Package Description: | 2500 mL in 1 BOTTLE, PLASTIC (66949-880-12) |
NDC Code | 66949-880-12 |
Proprietary Name | Zep Foam San |
Package Description | 2500 mL in 1 BOTTLE, PLASTIC (66949-880-12) |
Product NDC | 66949-880 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20030318 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Zep Inc. |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | .02 |
Strength Unit | g/10mL |
Pharmaceutical Classes |