| 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: | 66949-880-03 |
| Package Description: | 550 mL in 1 BOTTLE, PLASTIC (66949-880-03) |
| NDC Code | 66949-880-03 |
| Proprietary Name | Zep Foam San |
| Package Description | 550 mL in 1 BOTTLE, PLASTIC (66949-880-03) |
| 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 |