Label: AFLAC HAND SANITIZER 236ML 01- 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 11, 2020

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  • Drug Facts

    54860-247-01.jpg

  • Active Ingredient

    Medicinal Ingredients Purpose

    Ethyl Alcoh75% v/v Antibacterial

  • Warning

    Flammable,keep away from fire or flame.

    For external use only.

    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，Isopropyl Alcohol，Glycerin，Carbomer，Aminomethyl Propanol，Parfum，Propylene Glycol，ISOPROPYL MYRISTATE，ALOE BARBADENSIS LEAF JUICE，Tocopheryl Acetate，FD&C Yellow No.5(Tartrazine),FD&C Blue No.1.

  • USE

    For handwashing to decrease bacteria on the skin.

  • When using this product

    Avoid contact with eyes,if contact occurs,rinse eyes thoroughly with water.

  • Stop use and ask a doctor

    if irritation or rash develops and continues for more than 72 hours.

    Do not store above105℉

    May discolor some fabrics.

    Harmful to wood finishes and plastics.

  • Other information

  • Directions

    Take a palmful(5grams) of product in one hand

    Spread on both hands and rub into skin

  • Directions

    Take a palmful(5grams) of product in one hand

    Spread on both hands and rub into skin

  • PDP

    54860-247-01.jpg

  • INGREDIENTS AND APPEARANCE
    AFLAC HAND SANITIZER 236ML  01
    alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54860-247
    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
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.1 mL  in 100 mL
    ALOE (UNII: V5VD430YW9) 0.2 mL  in 100 mL
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) 0.001 mL  in 100 mL
    CARBOMER 940 (UNII: 4Q93RCW27E) 0.4 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 23.057972 mL  in 100 mL
    ISOPROPYL ALCOHOL (UNII: ND2M416302) 0.5 mL  in 100 mL
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M) 0.00002 mL  in 100 mL
    AMINOMETHYLPROPANOL (UNII: LU49E6626Q) 0.14 mL  in 100 mL
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD) 0.000008 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.5 mL  in 100 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.1 mL  in 100 mL
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.001 mL  in 100 mL
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54860-247-01236 mL in 1 BOTTLE; Type 0: Not a Combination Product05/11/2020
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart333A05/11/2020
    Labeler - Shenzhen Lantern Science Co.,Ltd (421222423)
    Registrant - Lantern Beauty America,INC. (117371139)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shenzhen Lantern Science Co., Ltd.421222423manufacture(54860-247)
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