Product NDC: | 52546-100 |
Proprietary Name: | Smith and Johnson Antibacterial |
Non Proprietary Name: | TRICLOSAN |
Active Ingredient(s): | .115 mL/100mL & nbsp; TRICLOSAN |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52546-100 |
Labeler Name: | Allied International Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20100621 |
Package NDC: | 52546-100-40 |
Package Description: | 1180 mL in 1 BOTTLE (52546-100-40) |
NDC Code | 52546-100-40 |
Proprietary Name | Smith and Johnson Antibacterial |
Package Description | 1180 mL in 1 BOTTLE (52546-100-40) |
Product NDC | 52546-100 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TRICLOSAN |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100621 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Allied International Corp |
Substance Name | TRICLOSAN |
Strength Number | .115 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |