| 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 |