Label: SANITIZE ASAP HAND SANITIZER- ethyl alcohol gel

  • 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 May 18, 2020

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  • Drug Facts

  • Active ingredient:

    Ethyl Alcohol Denatured.................80%

  • Purpose:

    Antiseptic

  • Inactive Ingredients:

    Deionized Water, Hydroxypropyl Cellulose, Glycerin, Hydrogen Peroxide.

  • INDICATIONS & USAGE

    Uses: to decrease bacteria on the skin that could interfere with good health, recommended for repeated use.

  • DOSAGE & ADMINISTRATION

    Directions: wet the hands thoroughly with the product and rub hands until dry.

  • WARNINGS

    Keep out of reach of children, keep out of the eyes, avoid contact with broken skin, if swallowed get medical help or contact a poison control center.

    Flammable, keep away from heat and flame.

  • SPL UNCLASSIFIED SECTION

    ANTI-BACTERIAL

    KILLS BACTERIA!

    MADE IN USA

    LABORATORY CRAFTED - ANTI-BACTERIAL BLEND

    FROM THE RESEARCH LABORATORIES OF NWH-USA

    BE SAFE

    BE CAUTIOUS

    These statements have not been evaluated by the Food and Drug Administration.

    This product is not intended to diagnose, treat cure or prevent any disease.

    SANITIZEASAP.COM

    New World Cosmetics and Medicinals.
    1080 Holland Drive. Suite 1,
    Boca Raton, Florida 33487

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    SANITIZE ASAP HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73871-378
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL0.8 mL  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    HYDROGEN PEROXIDE (UNII: BBX060AN9V)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73871-378-16473 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/01/2020
    Labeler - New World Holdings, Inc. (081183610)
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