Product NDC: | 55118-425 |
Proprietary Name: | Scott Antibacterial Foam |
Non Proprietary Name: | Triclosan |
Active Ingredient(s): | 5 g/L & nbsp; Triclosan |
Administration Route(s): | TOPICAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55118-425 |
Labeler Name: | Kimberly-Clark Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110201 |
Package NDC: | 55118-425-10 |
Package Description: | 1 L in 1 CARTRIDGE (55118-425-10) |
NDC Code | 55118-425-10 |
Proprietary Name | Scott Antibacterial Foam |
Package Description | 1 L in 1 CARTRIDGE (55118-425-10) |
Product NDC | 55118-425 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Triclosan |
Dosage Form Name | SOLUTION |
Route Name | TOPICAL |
Start Marketing Date | 20110201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Kimberly-Clark Corporation |
Substance Name | TRICLOSAN |
Strength Number | 5 |
Strength Unit | g/L |
Pharmaceutical Classes |