Label: UNITED AIRLINES CLEAN PLUS CLOROX- ethyl alcohol liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2024

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  • Uses:

    To help decrease bacteria on skin.

  • Warnings:

    Flammable.
    Keep away from fire or flame.
    For external use only.
    Do not use in eyese, in case of contact, rinse eyes thoroughly with water.
    Stop use and ask a doctor if skin irritation develops.

    Warnings:

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

  • Directions:

    Place/use enough product to cover hands, rub hands together until dry.
    Supervise children in the use of the product.

  • Drug Facts:

    Active Ingredients: Ethyl Alcohol 62% v/v

  • Inactive Ingredients:

    Aloe Barbadensis Leaf Extract
    Aqua

    Carbomer
    Glycerin

    Propylene Glycol

    Tocopheryl Acetate

    Triethanolamine

  • Other Information:

    Avoid extreme temperatures.

  • Purpose:

    Antibacterial

  • PRINCIPAL DISPLAY PANEL

    Does not contain bleach

    Label

    Listed on the label: Use enough product to cover the hands

  • INGREDIENTS AND APPEARANCE
    UNITED AIRLINES CLEAN PLUS CLOROX 
    ethyl alcohol liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52305-225
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL62 mL  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.001 mL  in 100 mL
    CARBOMER 934 (UNII: Z135WT9208) 0.28 mL  in 100 mL
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.001 mL  in 100 mL
    WATER (UNII: 059QF0KO0R) 37.307 mL  in 100 mL
    TROLAMINE (UNII: 9O3K93S3TK) 0.11 mL  in 100 mL
    GLYCERIN (UNII: PDC6A3C0OX) 0.3 mL  in 100 mL
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) 0.001 mL  in 100 mL
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52305-225-25250 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product08/28/2020
    Image of Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drug505G(a)(3)08/28/2020
    Labeler - Freshorize LLC (424168503)
    Registrant - Freshorize USA Ltd. (018206924)
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