Product NDC: | 0869-0876 |
Proprietary Name: | Rubbing |
Non Proprietary Name: | Ethyl Alcohol |
Active Ingredient(s): | 610 mg/mL & nbsp; Ethyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0869-0876 |
Labeler Name: | Vi-Jon |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 19890715 |
Package NDC: | 0869-0876-43 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (0869-0876-43) |
NDC Code | 0869-0876-43 |
Proprietary Name | Rubbing |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (0869-0876-43) |
Product NDC | 0869-0876 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Ethyl Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 19890715 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | Vi-Jon |
Substance Name | ALCOHOL |
Strength Number | 610 |
Strength Unit | mg/mL |
Pharmaceutical Classes |