Label: KEKE HAND SANITIZER 236ML 01- alcohol liquid

  • 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 May 25, 2020

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  • Drug Facts

    CH0006 label.jpg

  • Active Ingredient

    Active Ingredient Purpose

    Ethyl Alcohol 71%（w/w） Antiseptic

  • USE

    For hand sanitizing to reduce bacteria on the skin.

    Recommended for repeated use.

    use anywhere without water.

  • Warnings

    For external use only-hands.

    Flammable,keep away from heat and flame.

    For external use only.

    Flammable, keep away from heat and flame.

    Discontinue if skin becomes irritated and ask a doctor .

    Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a poson control center immediately.

  • Inactive ingredients

    Water, Parfum(Fragrance),Glycerin,Acrylates/C10-30 Alkyl Acrylate Crosspolymer,Aloe Yohjyu Matsu Ekisu,Aminomethyl Propanol,Tocopheryl Acetate.

  • Directions

    squeeze small amount in your palm and briskly rub hands together until dry.

    When using this product

    keep out of eyes. In case of contact with eyes, flush thoroughly with water.

    Do not inhale or ingest.

    Avoid contact with broken skin.

    Other information

    Do not store above 105F.

    May discolor some fabrics.

    Harmful to wood finishes and plastics.

  • Stop use and ask a doctor

    Stop use and ask a doctor if skin irritation develops.

  • Keep out of reach of children

    Keep out of reach of children

  • PRINCIPAL DISPLAY PANEL

    CH0006 label.jpg

  • INGREDIENTS AND APPEARANCE
    KEKE HAND SANITIZER 236ML  01
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-280
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL71 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS) 0.1 g  in 100 g
    ALOE (UNII: V5VD430YW9) 0.15 g  in 100 g
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.26 g  in 100 g
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.08 g  in 100 g
    WATER (UNII: 059QF0KO0R) 27.9 g  in 100 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 g  in 100 g
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 g  in 100 g
    Product Characteristics
    Colorwhite (transparant) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-280-01210 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product05/25/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/25/2020
    Labeler - Shenzhen Lantern Scicence Co.,Ltd. (421222423)
    Registrant - Lantern Beauty America,INC. (117371139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-280)
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