Product NDC: | 41520-165 |
Proprietary Name: | ANTIBACTERIAL FOAMING |
Non Proprietary Name: | TRICLOSAN |
Active Ingredient(s): | .46 mL/100mL & nbsp; TRICLOSAN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 41520-165 |
Labeler Name: | AMERICAN SALES COMPANY |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110516 |
Package NDC: | 41520-165-08 |
Package Description: | 221 mL in 1 BOTTLE, PUMP (41520-165-08) |
NDC Code | 41520-165-08 |
Proprietary Name | ANTIBACTERIAL FOAMING |
Package Description | 221 mL in 1 BOTTLE, PUMP (41520-165-08) |
Product NDC | 41520-165 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TRICLOSAN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20110516 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | AMERICAN SALES COMPANY |
Substance Name | TRICLOSAN |
Strength Number | .46 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |