Product NDC: | 63517-523 |
Proprietary Name: | Cardinal Health Sanitizer |
Non Proprietary Name: | ALCOHOL |
Active Ingredient(s): | .625 mg/mg & nbsp; ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | AEROSOL, FOAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63517-523 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20110224 |
Package NDC: | 63517-523-15 |
Package Description: | 12 BOTTLE, SPRAY in 1 CASE (63517-523-15) > 425000 mg in 1 BOTTLE, SPRAY |
NDC Code | 63517-523-15 |
Proprietary Name | Cardinal Health Sanitizer |
Package Description | 12 BOTTLE, SPRAY in 1 CASE (63517-523-15) > 425000 mg in 1 BOTTLE, SPRAY |
Product NDC | 63517-523 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ALCOHOL |
Dosage Form Name | AEROSOL, FOAM |
Route Name | TOPICAL |
Start Marketing Date | 20110224 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Cardinal Health |
Substance Name | ALCOHOL |
Strength Number | .625 |
Strength Unit | mg/mg |
Pharmaceutical Classes |