Label: GRAPEFRUIT HAND SANITIZER- ethyl alcohol gel

  • Category: HUMAN OTC DRUG LABEL

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 June 1, 2020

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  • Drug Facts

  • Active ingredient

    Ethyl Alcohol 70%

  • Purpose

    Antiseptic

  • Uses

    • To decrease bacteria on the skin that could cause disease.
    • When water, soap and towel are not available.
    • Recommended for repeated use.
  • Warnings

    For external use only: hands.

    Flammable. Keep away from fire or flame.

    When using this product • Keep out of eyes, ears, or mouth. • In case of eye contact, flush eyes thoroughly with water. • Avoid contact with broken skin. • Do not inhale or ingest.

    Stop use and ask a doctor if• redness or irritation develop

    • condition persists for more than 72 hours

    Keep out of reach of children.

    • Children should be supervised by an adult when using this product. • If swallowed, get medical help or contact a Poison Control Center right away.
  • Directions

    • Wet hand thoroughly with product and allow to dry without wiping. • No rinsing required. • For children under 6, use only under adult supervision. • Not recommended for infants.

  • Other information

    • Store below 105˚F(40˚C). • May discolor certain fabrics. • Harmful to wood finishes & plastics
  • Inactive ingredients:

    Water(Aqua), Triethanolamine, Carbomer, Aloe Barbadensis(Aloe Vera) Gel, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate(Vitamin E).

  • SPL UNCLASSIFIED SECTION

    Distributed by: East West Brands, Inc. New York, NY 10018

    UPC CODE

    PRO: 05/05/2020

    EXP: 04/05/2023

    MADE IN CHINA

    Kills 99.9% of Germs

    WITH ALOE & VITAMIN E

  • Packaging

    IMAGE

  • INGREDIENTS AND APPEARANCE
    GRAPEFRUIT HAND SANITIZER 
    ethyl alcohol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73960-004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL70 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73960-004-01237 mL in 1 BOTTLE; Type 0: Not a Combination Product06/01/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A06/01/2020
    Labeler - East West Brands Inc. (080642088)
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