Product NDC: | 75981-370 |
Proprietary Name: | Advanced |
Non Proprietary Name: | Ethyl Alcohol |
Active Ingredient(s): | 70 kg/100L & nbsp; Ethyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75981-370 |
Labeler Name: | Geiss, Destin + Dunn, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120920 |
Package NDC: | 75981-370-34 |
Package Description: | .236 L in 1 BOTTLE, PLASTIC (75981-370-34) |
NDC Code | 75981-370-34 |
Proprietary Name | Advanced |
Package Description | .236 L in 1 BOTTLE, PLASTIC (75981-370-34) |
Product NDC | 75981-370 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl Alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120920 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Geiss, Destin + Dunn, Inc |
Substance Name | ALCOHOL |
Strength Number | 70 |
Strength Unit | kg/100L |
Pharmaceutical Classes |