Label: HAND SANITIZER- isopropyl alcohol spray

  • NDC Code(s): 50405-016-01, 50405-016-02
  • Packager: SOHM Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 12, 2024

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  • Active Ingredient(s)

    Isopropyl Alcohol 67% v/v. Purpose: Antiseptic

  • Purpose

    Antiseptic, Hand Sanitizer

  • Use

    Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

  • Warnings

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

  • Do not use

    • Do not use on children under 2 years.
  • WHEN USING

    Avoid contact with eyes.


    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 this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Cover hands with product by thoroughly rubbing and allow to air dry without wipping. Wash hands with soap and water at the earliest opportunity.
  • Other information

    • Store at 30°C (86°F). keep out of direct sunlight.
  • Inactive ingredients

    Water, Glycerin, Propylene Glycol, Aloe Barbadensis (Aloe vera) gel, Tocopheryl acetate

  • Package Label - Principal Display Panel

    9 mL NDC: 50405-016-01

    9ml-spray

  • Package Label - Principal Display Panel

    236 mL; NDC 50405-016-02

    236ml-spray

  • INGREDIENTS AND APPEARANCE
    HAND SANITIZER 
    isopropyl alcohol spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50405-016
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ISOPROPYL ALCOHOL (UNII: ND2M416302) (ISOPROPYL ALCOHOL - UNII:ND2M416302) ISOPROPYL ALCOHOL67 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:50405-016-019 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/10/202012/31/2023
    2NDC:50405-016-02236 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product09/10/202012/31/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00309/10/202012/31/2023
    Labeler - SOHM Inc (009303848)
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