Product NDC: | 25382-505 |
Proprietary Name: | Mysotrol No Rinse Antiseptic Hand Cleanser |
Non Proprietary Name: | Ethyl Alcohol |
Active Ingredient(s): | 62 mL/100mL & nbsp; Ethyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 25382-505 |
Labeler Name: | Derma Sciences |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20061201 |
Package NDC: | 25382-505-04 |
Package Description: | 118 mL in 1 BOTTLE (25382-505-04) |
NDC Code | 25382-505-04 |
Proprietary Name | Mysotrol No Rinse Antiseptic Hand Cleanser |
Package Description | 118 mL in 1 BOTTLE (25382-505-04) |
Product NDC | 25382-505 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl Alcohol |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20061201 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Derma Sciences |
Substance Name | ALCOHOL |
Strength Number | 62 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |