Label: MIRACLE AQUA PEELING- hyaluronate sodium gel

  • 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 September 20, 2018

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  • ACTIVE INGREDIENT

    Sodium Hyaluronate 0.005%

  • PURPOSE

    Moisturizing

  • INDICATIONS & USAGE

    Helps to keep skin moistness

  • DOSAGE & ADMINISTRATION

    Apply a generous amount on face and gently massage.
    Rinse thoroughly.

  • WARNINGS

    For external use only.
    Do not use on damaged or broken skin.
    When using this product, keep out of eyes. Rinse with water to remove.
    Stop using and ask a doctor if rash occurs.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

  • INACTIVE INGREDIENT

    Water, 1,2-Hexanediol, Alcohol, Arginine, Butylene Glycol, Camellia Sinensis Leaf Extract, Canavalia Gladiata Seed Extract, Carbomer, Caviar Extract, Cellulose, Centella Asiatica Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ethylhexylglycerin, Fragrance, Glycyrrhiza Glabra (Licorice) Root Extract, Nasturtium Offcinale Extract, PEG-400, PEG-60 Hydrogenated Castor Oil , Polygonum Cuspidatum Root Extract, Rosmarinus Officinalis (Rosemary) Leaf Exreact, Scutellaria Baicalensis Root Extract, Tocopheryl Acetate

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    MIRACLE AQUA PEELING 
    hyaluronate sodium gel
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72557-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.005 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    ALCOHOL (UNII: 3K9958V90M)  
    ARGININE (UNII: 94ZLA3W45F)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    CAVIAR, UNSPECIFIED (UNII: 020K6HLU0O)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72557-001-01100 g in 1 CONTAINER; Type 0: Not a Combination Product09/19/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/19/2018
    Labeler - TOAS Co., Ltd. (694485346)
    Registrant - TOAS Co., Ltd. (694485346)
    Establishment
    NameAddressID/FEIBusiness Operations
    TOAS Co., Ltd.694485346manufacture(72557-001)