| Product NDC: | 49794-010 |
| Proprietary Name: | Antibacterial |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 620 g/L & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 49794-010 |
| 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: | 49794-010-99 |
| Package Description: | 1100 L in 1 CONTAINER (49794-010-99) |
| NDC Code | 49794-010-99 |
| Proprietary Name | Antibacterial |
| Package Description | 1100 L in 1 CONTAINER (49794-010-99) |
| Product NDC | 49794-010 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | LIQUID |
| 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/L |
| Pharmaceutical Classes |