NDC 52000-001

Allure Isopropyl Rubbing Alcohol

Isopropyl Alcohol

Allure Isopropyl Rubbing Alcohol is a Topical Liquid in the Human Otc Drug category. It is labeled and distributed by Universal Distribution Center Llc. The primary component is Isopropyl Alcohol.

Product ID52000-001_6dffaf6a-8fa0-4606-a9d9-39929810082f
NDC52000-001
Product TypeHuman Otc Drug
Proprietary NameAllure Isopropyl Rubbing Alcohol
Generic NameIsopropyl Alcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2012-06-29
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH FINAL
Application Numberpart333A
Labeler NameUniversal Distribution Center LLC
Substance NameISOPROPYL ALCOHOL
Active Ingredient Strength50 mL/100mL
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 52000-001-01

118 mL in 1 BOTTLE, PLASTIC (52000-001-01)
Marketing Start Date2012-06-29
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52000-001-05 [52000000105]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-06 [52000000106]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-01 [52000000101]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-07 [52000000107]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-03 [52000000103]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-02 [52000000102]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

NDC 52000-001-04 [52000000104]

Allure Isopropyl Rubbing Alcohol LIQUID
Marketing CategoryOTC monograph final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2012-06-29
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ISOPROPYL ALCOHOL50 mL/100mL

OpenFDA Data

SPL SET ID:73ad28c6-71e6-41df-a9a2-22834ccef107
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 616456
    • UPC Code
  • 0676979860015

    • NDC Crossover Matching brand name "Allure Isopropyl Rubbing Alcohol" or generic name "Isopropyl Alcohol"

    NDCBrand NameGeneric Name
    52000-001Allure Isopropyl Rubbing AlcoholAllure Isopropyl Rubbing Alcohol
    0363-081070%Isopropyl alcohol
    0363-084570% RubbingIsopropyl Alcohol
    0395-9103Ear Drops for SwimmersIsopropyl Alcohol
    0065-9800HAND SANITIZERIsopropyl Alcohol
    0395-1211HUMCO 1 Percent IodineIsopropyl Alcohol
    0395-0098HUMCO Ear Drops for SwimmersIsopropyl Alcohol
    0395-1249HUMCO Isopropyl Rubbing Alcohol 70%Isopropyl Alcohol
    0395-4202HUMCO Isopropyl Rubbing Alcohol 70% Professional PackIsopropyl Alcohol
    0168-0907Isopropyl AlcoholIsopropyl Alcohol
    0363-0275Isopropyl alcoholIsopropyl alcohol
    0363-0277Isopropyl alcoholIsopropyl alcohol
    0363-0472Isopropyl alcoholIsopropyl alcohol
    0363-0804Isopropyl AlcoholIsopropyl Alcohol
    0395-1260Isopropyl Alcohol Antiseptic 75% Topical SolutionIsopropyl Alcohol
    0363-0809Walgreen AlcoholIsopropyl Alcohol
    0363-6505Walgreens 70% Isopropyl Alcohol WipesISOPROPYL ALCOHOL
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