Label: MIRACLE LASER SKIN MIST- niacinamide liquid

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

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 24, 2018

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  • ACTIVE INGREDIENT

    Niacinamide 0.5%

  • PURPOSE

    Brightening

  • INDICATIONS & USAGE

    Helps brightness

  • DOSAGE & ADMINISTRATION

    Close eyes and gently mist the face after cleansing

  • 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, Rosa Centifolia Flower Water, Butylene Glycol, Aloe Barbadensis Leaf Extract, Hamamelis Virginiana (Witch Hazel) Leaf Extract, Propylene Glycol, 1,2-Hexanediol, PEG-60 Hydrogenated Castor Oil , Centella Asiatica Extract, Acorus Calamus Root Extract, Camellia Japonica Flower Extract, Canavalia Gladiata Seed Extract, Caviar Extract, Fragrance, Hizikia Fusiforme Extract, Lonicera Japonica (Honeysuckle) Flower Extract , Nasturtium Offcinale Extract, Salvia Officinalis (Sage) Extract , Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Exreact, Lecithin, Glycerin, Adenosine, Sodium Hyaluronate, Hydrogenated Lecithin, Ethylhexylglycerin, Oligopeptide-1

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    MIRACLE LASER SKIN MIST 
    niacinamide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72557-003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE0.6 mg  in 120 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HAMAMELIS VIRGINIANA LEAF (UNII: T07U1161SV)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    PEG-60 HYDROGENATED CASTOR OIL (UNII: 02NG325BQG)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    ROSA CENTIFOLIA FLOWER (UNII: CS4TE8FF7O)  
    ACORUS CALAMUS ROOT (UNII: XY1K7KIQ0F)  
    CAMELLIA JAPONICA FLOWER (UNII: KUB8101TNF)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72557-003-01120 mL in 1 CONTAINER; Type 0: Not a Combination Product09/24/2018
    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(72557-003)