Label: 1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E- alcohol gel

  • NDC Code(s): 22431-020-01
  • Packager: BLUE CROSS LABORATORIES, INC.
  • 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 December 15, 2017

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  • Kills Over 99% of Most Common Germs within seconds

    Armstrong allows you to wash your hands whenever conventional soap and water is not available. Use as an aid to reduce exposure to infectious germs and to supplement daily handwashing. Helps meet U.S. Government standards by protecting against exposure to bloodborne diseases. Nontozic-For External Use Only.

    Keep bottle of Armstrong in

    • Kitchen Medical Offices Nurseries
    • Automobile Bathrooms Workplace
  • Drug Facts Active Ingredients

    Ethyl Alcohol 65%

  • Purpose

    Antimicrobial

  • Directions:

    • Put a thumbnail size amount in your palm and rub your hands together briskly until dry.
    • Children 6 years of age should be supervised when using Armstrong.

  • Inactive Ingredients:

    Water (Aqua),Aloe Barbadensis Leaf Juice, Carbomer,Fragrance,Glycerin,Propylene Glycol,Tocopheryl Acetate,Triethanolamine.

  • Warning

    • Flammable, keep away from flame.
    • Keep out of eyes. In case of eye contact immediately flush eyes with water then contact physician.
    • If swallowed, contact physician.
    • For External Use Only.
    • Do not store above 110℉。
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.

  • 1.8oz Armstrong Hand Sanitizer

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    1.8OZ ARMSTRONG HAND SANITIZER WITH ALOE VERA AND VITAMIN E 
    alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:22431-020
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL65 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R) 33 mL  in 100 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:22431-020-0153 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product10/25/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A10/25/2017
    Labeler - BLUE CROSS LABORATORIES, INC. (008298879)
    Registrant - NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD. (530766098)
    Establishment
    NameAddressID/FEIBusiness Operations
    NINGBO LIYUAN DAILY CHEMICAL PRODUCTS CO., LTD.530766098manufacture(22431-020)
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