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 |