Product NDC: | 11822-4803 |
Proprietary Name: | RITE AID RENEWAL |
Non Proprietary Name: | ETHYL ALCOHOL |
Active Ingredient(s): | 700 mg/mL & nbsp; ETHYL ALCOHOL |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11822-4803 |
Labeler Name: | RITE AID CORPORATION |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333E |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20120318 |
Package NDC: | 11822-4803-2 |
Package Description: | 946 mL in 1 BOTTLE, PLASTIC (11822-4803-2) |
NDC Code | 11822-4803-2 |
Proprietary Name | RITE AID RENEWAL |
Package Description | 946 mL in 1 BOTTLE, PLASTIC (11822-4803-2) |
Product NDC | 11822-4803 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | ETHYL ALCOHOL |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120318 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | RITE AID CORPORATION |
Substance Name | ALCOHOL |
Strength Number | 700 |
Strength Unit | mg/mL |
Pharmaceutical Classes |