Label: ATONO2 OXYGEN PURE BATH AND- glycerin shampoo

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

Drug Label Information

Updated October 13, 2016

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  • ACTIVE INGREDIENT

    Glycerin

  • INACTIVE INGREDIENT

    Lauric Acid, Cocamide Methyl MEA, Potassium Hydroxide, Decyl Glucoside, Sodium Chloride, Myristic Acid, Beta-Glucan, etc.

  • PURPOSE

    Skin Protectant

  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    Take an appropriate amount and work up a lather. Then gently massage onto the whole body and rinse with 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 PURE BATH AND 
    glycerin shampoo
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70993-0009
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN3.845 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    LAURIC ACID (UNII: 1160N9NU9U)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:70993-0009-1300 g 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 other09/01/2015
    Labeler - LAORGANIC Co., Ltd. (689844148)
    Registrant - LAORGANIC Co., Ltd. (689844148)
    Establishment
    NameAddressID/FEIBusiness Operations
    LAORGANIC Co., Ltd.689844148manufacture(70993-0009)
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