Label: ATONO2 OXYGEN BUBBLE FOAM- glycerin liquid

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated October 12, 2016

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  • ACTIVE INGREDIENT

    Glycerin

  • INACTIVE INGREDIENT

    Disodium Cocoyl Glutamate, Decyl Glucoside, Potassium Cocoyl Glycinate, Disodium Cocoamphodiacetate, Betaine, Potassium Cocoate, Panthenol, etc.

  • PURPOSE

    Skin Protectant

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Pump an appropriate amount and gently massage the wet facial skin with it. Then rinse with warm water.

  • WARNINGS

    • For external use only
    • When using this product

    1. If any one of following symptoms occurs when using cosmetics, stop using it and consult a dermatologist.
    A. red spot, swelling, itching, stimulus
    B. symptoms mentioned above are caused by sunlight.

    2. Do not apply on skin where there is wound, eczema, or irritation.

    3. Storage and cautions for handling
    A. Close stopper after using.
    B. Keep out of reach of children.
    C. Keep away from high or low temperature and direct sunlight.

    4. This is not a medicinal product. Made of 100% cosmetic ingredients, it is a sensitive-skin care product for all skin types.

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    l

  • INGREDIENTS AND APPEARANCE
    ATONO2 OXYGEN BUBBLE FOAM 
    glycerin liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70993-0004
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3.075 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BETAINE (UNII: 3SCV180C9W)  
    WATER (UNII: 059QF0KO0R)  
    DECYL GLUCOSIDE (UNII: Z17H97EA6Y)  
    DISODIUM COCOYL GLUTAMATE (UNII: MBK0CP8F5A)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70993-0004-1150 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product09/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other11/01/2014
    Labeler - LAORGANIC Co., Ltd. (689844148)
    Registrant - LAORGANIC Co., Ltd. (689844148)
    Establishment
    NameAddressID/FEIBusiness Operations
    LAORGANIC Co., Ltd.689844148manufacture(70993-0004)
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