Label: ANTHEM HAND SANITIZER 500ML- alcohol liquid

  • 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 6, 2020

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  • Drug Facts

    Anthem hand sanitizer 500ml

  • Ingredient

    Active Ingredient Purpose

    Ethyl Alcohol 75%（V/V） Antiseptic

  • USE

    For external use only-hands.

    Flammable

    Keep away from heat and flame.

    Recommended for repeated use.

    use anywhere without water.

  • Warning

    For external use only-hands.

    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 Poison Control Center immediately.

    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

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

  • 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.

  • PRINCIPAL DISPLAY PANEL

    Anthem hand sanitizer 500ml

  • INGREDIENTS AND APPEARANCE
    ANTHEM HAND SANITIZER 500ML 
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-249
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL75 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.01 mL  in 100 mL
    ALOE ANDONGENSIS WHOLE (UNII: XOQ5N25YKS) 0.01 mL  in 100 mL
    ALOE (UNII: V5VD430YW9) 0.15 mL  in 100 mL
    CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO) 0.3 mL  in 100 mL
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.09 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 23.85 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 100 mL
    Product Characteristics
    Colorwhite (transparant) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-249-01500 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/24/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A04/24/2020
    Labeler - Shenzhen Lantern Scicence Co Ltd (421222423)
    Registrant - Lantern Beauty America,INC. (117371139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co.,Ltd.421222423manufacture(54860-249)
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