Label: BEAUHYANG DAILY SUM HAND SANITIZER GEL- ethanol 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 April 3, 2020

If you are a consumer or patient please visit this version.

  • Drug Facts

  • Active ingredients

    Ethanol 67.7% (v/v)

  • Purpose

    Antimicrobial

  • Use

    Hand sanitizer to help reduce bacteria on the skin

  • Warnings

    Flammable. Keep away from fire or flame.

    For external use only 

    When using this product do not use in or near eyes. In case of contact, rinse eyes thoroughly with water.

    Stop use and ask a doctor if irritation or rash appears and lasts

    Keep out of reach of children. If inhaled or swallowed, get medical help or contact a Poison Control Center right away

  • Directions

    • Put enough product in your palm to cover hands and rub hands together briskly until dry

    • Children under 6 years of age should be supervised when using this product

  • Other information

    • Store at room temperature (33.8°F - 86°F, 1°C - 30°C) and avoid cold or dry place. 

  • Inactive ingredients

    Water (30.879%), Glycerin (0.87%), Tocopheryl Acetate (0.01%), Carbomer (0.27%), Triethanolamine (0.27%), Hyaluronic acid (0.001%) 

  • SPL UNCLASSIFIED SECTION

    FLiNT

    KILLS MORE THAN GERMS

    LEAVES HANDS FEELING CLEAN & SOFT

    VITAMIN E, SULFATE-FREE & PARABEN-FREE

    Hand disinfectant with rich moisturizing ingredient

    KILLS MOST COMMON GERMS THAT MAY CAUSE ILLNESS IN 30 SECONDS

    Made in KOREA

    U.S. Distributor: FLINT MATERIALS CO LLC., Cochran, GA 31014 U.S.A

    Question?  www.flinthygiene.com

  • Packaging

    image description

  • INGREDIENTS AND APPEARANCE
    BEAUHYANG DAILY SUM HAND SANITIZER GEL 
    ethanol gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73892-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL67.7 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73892-0003-1500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product03/28/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A03/28/2020
    Labeler - JUHWANBIO.CELL CO.,LTD. (690163444)
    Establishment
    NameAddressID/FEIBusiness Operations
    JUHWANBIO.CELL CO.,LTD.690163444manufacture(73892-0003)