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TopSani
TopSani - 24439-321-10 - (Benzalkonium Chloride)
Drug Information of TopSani
| 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) |
Labeler Information of TopSani
| 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 Information of TopSani
| Package NDC: | 24439-321-10 |
| Package Description: | 56 mL in 1 BOTTLE, PLASTIC (24439-321-10) |
NDC Information of TopSani
| NDC Code | 24439-321-10 |
| Proprietary Name | TopSani |
| Package Description | 56 mL in 1 BOTTLE, PLASTIC (24439-321-10) |
| 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 |
