| Product NDC: | 43374-575 |
| Proprietary Name: | Quik San |
| Non Proprietary Name: | BENZETHONIUM CHLORIDE |
| Active Ingredient(s): | 2 mg/mL & nbsp; BENZETHONIUM CHLORIDE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 43374-575 |
| Labeler Name: | Delta Foremost Chemical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20090831 |
| Package NDC: | 43374-575-18 |
| Package Description: | 50 mL in 1 BOTTLE, PLASTIC (43374-575-18) |
| NDC Code | 43374-575-18 |
| Proprietary Name | Quik San |
| Package Description | 50 mL in 1 BOTTLE, PLASTIC (43374-575-18) |
| Product NDC | 43374-575 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | BENZETHONIUM CHLORIDE |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20090831 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Delta Foremost Chemical Corporation |
| Substance Name | BENZETHONIUM CHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |