Label: MIRACLE LASER MASK- hyaluronate sodium cream

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

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Drug Label Information

Updated September 24, 2018

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  • ACTIVE INGREDIENT

    Sodium Hyaluronate 0.005%

  • PURPOSE

    Moisturizing

  • INDICATIONS & USAGE

    Helps to keep skin moistness

  • DOSAGE & ADMINISTRATION

    Remove film and apply mask over cleansed face. Leave on for 15-30 minutes then remove.

  • 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, Glycerin, Butylene Glycol, Propylene Glycol, Aloe Barbadensis Leaf Extract, Portulaca Oleracea Extract, Arginine, Carbomer, Polysorbate 80, Betaine, Allantoin, Methylparaben, Hydrolyzed Collagen, Sodium PCA, Disodium EDTA, Dipotassium Glycyrrhizate, Hamamelis Virginiana (Witchhazel) Water, Tocopheryl Acetate, Sodium Polyacrylate, Fragrance, Propylparaben, OligoPepTide-1

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    MIRACLE LASER MASK 
    hyaluronate sodium cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72557-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.0014 g  in 28 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    ARGININE (UNII: 94ZLA3W45F)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    BETAINE (UNII: 3SCV180C9W)  
    ALLANTOIN (UNII: 344S277G0Z)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72557-005-0210 in 1 CARTON09/24/2018
    1NDC:72557-005-0128 g in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/24/2018
    Labeler - TOAS Co., Ltd. (694485346)
    Registrant - TOAS Co., Ltd. (694485346)
    Establishment
    NameAddressID/FEIBusiness Operations
    TOAS Co., Ltd.694485346manufacture(72557-005)
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