Label: ARMICARE HAND SANITIZER- alcohol liquid

  • NDC Code(s): 81793-187-00, 81793-187-03
  • Packager: Armis Biopharma, Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 6, 2024

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  • DRUG FACTS

  • ACTIVE INGREDIENT

    Ethyl Alcohol 75% v/v.

    PURPOSE

    Antiseptic

  • USES

    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

    • On children less than 2 months of age
    • On open skin wounds

    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 at 1-800-222-1222

  • 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:

    Deionized water, Glycerin, Hydrogen Peroxide, Acetic Acid, Lavender, Polysorbate-20

  • QUESTIONS?

    1-800-970-1779

  • Package Labeling:

    Label

  • Package Labeling:

    Label2

  • INGREDIENTS AND APPEARANCE
    ARMICARE HAND SANITIZER 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:81793-187
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    ACETIC ACID (UNII: Q40Q9N063P)  
    LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER (UNII: 19AH1RAF4M)  
    POLYSORBATE 20 (UNII: 7T1F30V5YH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:81793-187-0060 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product04/05/2021
    2NDC:81793-187-0389 mL in 1 TUBE; Type 0: Not a Combination Product02/12/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)04/05/2021
    Labeler - Armis Biopharma, Inc (166990189)
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