Label: 32OZ ISOPROPYL ALCOHOL liquid

  • NDC Code(s): 90055-206-32
  • Packager: Collective Science Integration
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated September 25, 2020

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  • DOSAGE & ADMINISTRATION

    Dosage and Administration

  • INACTIVE INGREDIENT

    Inactive Ingredients

  • INDICATIONS & USAGE

    Indications

  • ACTIVE INGREDIENT

    Active

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach

  • PURPOSE

    Purpose

  • WARNINGS

    Warnings

  • PRINCIPAL DISPLAY PANEL

    PDP

  • INGREDIENTS AND APPEARANCE
    32OZ ISOPROPYL ALCOHOL 
    32oz isopropyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:90055-206
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL70 mL  in 70 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:90055-206-32946 mL in 1 BOTTLE; Type 0: Not a Combination Product09/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A09/24/2020
    Labeler - Collective Science Integration (133591508)
    Establishment
    NameAddressID/FEIBusiness Operations
    P&P International133591508manufacture(90055-206)