Product NDC: | 52000-002 |
Proprietary Name: | Allure Isopropyl Rubbing Alcohol With Wintergreen |
Non Proprietary Name: | Isopropyl Alcohol |
Active Ingredient(s): | 50 mL/100mL & nbsp; Isopropyl Alcohol |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 52000-002 |
Labeler Name: | Universal Distribution Center LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333A |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20120630 |
Package NDC: | 52000-002-04 |
Package Description: | 296 mL in 1 BOTTLE, PLASTIC (52000-002-04) |
NDC Code | 52000-002-04 |
Proprietary Name | Allure Isopropyl Rubbing Alcohol With Wintergreen |
Package Description | 296 mL in 1 BOTTLE, PLASTIC (52000-002-04) |
Product NDC | 52000-002 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Isopropyl Alcohol |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20120630 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Universal Distribution Center LLC |
Substance Name | ISOPROPYL ALCOHOL |
Strength Number | 50 |
Strength Unit | mL/100mL |
Pharmaceutical Classes |