Label: RUBBING ALCOHOL- alcohol liquid

  • NDC Code(s): 78440-009-01
  • Packager: INTERNATIONAL GENERAL TRADING CORP
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Active Ingredient(s)

    Isopropyl Alcohol 50% v/v. Purpose: Antiseptic

  • Purpose

    aNTIMICROBIAL

  • Use

    DECREASE GERMS IN MINOR CUTS AND HELPS RELIEVE MINO MUSCULAR ACHES DUE TO EXERTION

  • Warnings

    For external use only. Flammable. Keep away from heat or flame

  • Do not use

    • in children less than 2 months of age
    • on open skin wounds
  • WHEN USING

    When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • STOP USE

    Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Place enough product on hands to cover all surfaces. Rub hands together until dry.
    • Supervise children under 6 years of age when using this product to avoid swallowing.
  • Other information

    • Store between 15-30C (59-86F)
    • Avoid freezing and excessive heat above 40C (104F)
  • Inactive ingredients

    WATER

  • Package Label - Principal Display Panel

    50ALCOHOL354 ML

  • INGREDIENTS AND APPEARANCE
    RUBBING ALCOHOL 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:78440-009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL50 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:78440-009-01354 mL in 1 BOTTLE; Type 0: Not a Combination Product03/12/2021
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00303/12/2021
    Labeler - INTERNATIONAL GENERAL TRADING CORP (825499598)
    Registrant - INTERNATIONAL GENERAL TRADING CORP (825499598)
    Establishment
    NameAddressID/FEIBusiness Operations
    JELL PHARMACEUTICALS PRIVATE LIMITED726025211manufacture(78440-009)
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