| Product NDC: | 20276-054 |
| Proprietary Name: | Lucky |
| Non Proprietary Name: | Ethyl Alcohol |
| Active Ingredient(s): | 70 mL/100mL & nbsp; Ethyl Alcohol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 20276-054 |
| Labeler Name: | Delta Brands Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333A |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20121030 |
| Package NDC: | 20276-054-10 |
| Package Description: | 295 mL in 1 BOTTLE, PUMP (20276-054-10) |
| NDC Code | 20276-054-10 |
| Proprietary Name | Lucky |
| Package Description | 295 mL in 1 BOTTLE, PUMP (20276-054-10) |
| Product NDC | 20276-054 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Ethyl Alcohol |
| Dosage Form Name | LIQUID |
| Route Name | TOPICAL |
| Start Marketing Date | 20121030 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | Delta Brands Inc. |
| Substance Name | ALCOHOL |
| Strength Number | 70 |
| Strength Unit | mL/100mL |
| Pharmaceutical Classes |