Home > National Drug Code (NDC) > Allure Isopropyl Rubbing Alcohol

Allure Isopropyl Rubbing Alcohol - 52000-001-01 - (Isopropyl Alcohol)

Alphabetical Index


Drug Information of Allure Isopropyl Rubbing Alcohol

Product NDC: 52000-001
Proprietary Name: Allure Isopropyl Rubbing Alcohol
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)

Labeler Information of Allure Isopropyl Rubbing Alcohol

Product NDC: 52000-001
Labeler Name: Universal Distribution Center LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: part333A
Marketing Category: OTC MONOGRAPH FINAL
Start Marketing Date: 20120629

Package Information of Allure Isopropyl Rubbing Alcohol

Package NDC: 52000-001-01
Package Description: 118 mL in 1 BOTTLE, PLASTIC (52000-001-01)

NDC Information of Allure Isopropyl Rubbing Alcohol

NDC Code 52000-001-01
Proprietary Name Allure Isopropyl Rubbing Alcohol
Package Description 118 mL in 1 BOTTLE, PLASTIC (52000-001-01)
Product NDC 52000-001
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Isopropyl Alcohol
Dosage Form Name LIQUID
Route Name TOPICAL
Start Marketing Date 20120629
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

Complete Information of Allure Isopropyl Rubbing Alcohol


General Information