| Product NDC: | 49794-009 |
| Proprietary Name: | Antibacterial |
| Non Proprietary Name: | Alcohol |
| Active Ingredient(s): | 620 g/kg & nbsp; Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49794-009 |
| Labeler Name: | Continental Manufacturing Chemist, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110901 |
| Package NDC: | 49794-009-99 |
| Package Description: | 1000 kg in 1 CONTAINER (49794-009-99) |
| NDC Code | 49794-009-99 |
| Proprietary Name | Antibacterial |
| Package Description | 1000 kg in 1 CONTAINER (49794-009-99) |
| Product NDC | 49794-009 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Alcohol |
| Dosage Form Name | GEL |
| Route Name | TOPICAL |
| Start Marketing Date | 20110901 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Continental Manufacturing Chemist, Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 620 |
| Strength Unit | g/kg |
| Pharmaceutical Classes |