NDC 52000-030

Isopropyl Rubbing Alcohol 99%

Isopropyl Alcohol

Isopropyl Rubbing Alcohol 99% 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 ID52000-030_407ca437-f731-601d-e054-00144ff88e88
NDC52000-030
Product TypeHuman Otc Drug
Proprietary NameIsopropyl Rubbing Alcohol 99%
Generic NameIsopropyl Alcohol
Dosage FormLiquid
Route of AdministrationTOPICAL
Marketing Start Date2016-11-04
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart333A
Labeler NameUniversal Distribution Center LLC
Substance NameISOPROPYL ALCOHOL
Active Ingredient Strength99 mL/100mL
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 52000-030-01

118 mL in 1 BOTTLE, PLASTIC (52000-030-01)
Marketing Start Date2016-11-04
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 52000-030-04 [52000003004]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-06 [52000003006]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-01 [52000003001]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-07 [52000003007]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-05 [52000003005]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-03 [52000003003]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

NDC 52000-030-02 [52000003002]

Isopropyl Rubbing Alcohol 99% LIQUID
Marketing CategoryOTC monograph not final
Application Numberpart333A
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-11-04
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ISOPROPYL ALCOHOL99 mL/100mL

OpenFDA Data

SPL SET ID:a6d082ac-47b1-4847-b075-630892071885
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 402481
  • UPC Code
  • 0676979860794
  • NDC Crossover Matching brand name "Isopropyl Rubbing Alcohol 99%" or generic name "Isopropyl Alcohol"

    NDCBrand NameGeneric Name
    52000-030Isopropyl Rubbing Alcohol 99%Isopropyl Rubbing Alcohol 99%
    75983-007Isopropyl Rubbing Alcohol 99%Isopropyl Rubbing Alcohol 99%
    52000-049Isopropyl Rubbing Alcohol 99%Isopropyl Rubbing Alcohol 99%
    52862-027Isopropyl Rubbing Alcohol 99%Isopropyl Rubbing Alcohol 99%
    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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