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 |