Product NDC: | 51042-692 |
Proprietary Name: | First Mark |
Non Proprietary Name: | Benzethonium Chloride |
Active Ingredient(s): | .2 mL/100mL & nbsp; Benzethonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51042-692 |
Labeler Name: | Performance Food Group |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100623 |
Package NDC: | 51042-692-17 |
Package Description: | 50 mL in 1 BOTTLE, PUMP (51042-692-17) |
NDC Code | 51042-692-17 |
Proprietary Name | First Mark |
Package Description | 50 mL in 1 BOTTLE, PUMP (51042-692-17) |
Product NDC | 51042-692 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzethonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100623 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Performance Food Group |
Substance Name | BENZETHONIUM CHLORIDE |
Strength Number | .2 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |