Product NDC: | 24439-321 |
Proprietary Name: | TopSani |
Non Proprietary Name: | Benzalkonium Chloride |
Active Ingredient(s): | 1.25 mL/1000mL & nbsp; Benzalkonium Chloride |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 24439-321 |
Labeler Name: | United Promotions Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20111101 |
Package NDC: | 24439-321-11 |
Package Description: | 236 mL in 1 BOTTLE, PUMP (24439-321-11) |
NDC Code | 24439-321-11 |
Proprietary Name | TopSani |
Package Description | 236 mL in 1 BOTTLE, PUMP (24439-321-11) |
Product NDC | 24439-321 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Benzalkonium Chloride |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20111101 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | United Promotions Inc. |
Substance Name | BENZALKONIUM CHLORIDE |
Strength Number | 1.25 |
Strength Unit | mL/1000mL |
Pharmaceutical Classes |