Label: MOISTURE BOUND- tremella fuciformis whole, niacinamide, adenosine, ceramide cream

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

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Drug Label Information

Updated July 4, 2017

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  • ACTIVE INGREDIENT

    Tremella Fuciformis Whole, Niacinamide, Adenosine, Ceramide

  • INACTIVE INGREDIENT

    Water, Glycerin, Butylene Glycol, etc

  • PURPOSE

    Skin protectant - Anti Wrinkle, Whitening

    Daily moisturizer that can be used day and night

  • KEEP OUT OF REACH OF CHILDREN

    keep out or reach of the children

  • INDICATIONS & USAGE

    After Cleansing your face, apply after applying serum.

    Can be used as a mask when applied generously.

  • WARNINGS

    • For external use only.
    • Do not use on damaged or broken skin.
    • If any signs of the following skin troubles apprear, stop use and talk yo your dermatologist.
    1. Rash
    2. Itching
    3. Irritation
    • Avoid placing this product in this container in the excessive heat or direct sun
  • DOSAGE & ADMINISTRATION

    for external use only


  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    MOISTURE BOUND 
    tremella fuciformis whole, niacinamide, adenosine, ceramide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71496-0001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    TREMELLA FUCIFORMIS WHOLE (UNII: 4938BNS0GU) (TREMELLA FUCIFORMIS WHOLE - UNII:4938BNS0GU) TREMELLA FUCIFORMIS WHOLE0.1 g  in 100 mL
    CERAMIDE NP (UNII: 4370DF050B) (CERAMIDE NP - UNII:4370DF050B) CERAMIDE NP0.01 g  in 100 mL
    NIACINAMIDE (UNII: 25X51I8RD4) (NIACINAMIDE - UNII:25X51I8RD4) NIACINAMIDE2 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71496-0001-150 mL in 1 JAR; Type 0: Not a Combination Product07/05/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/05/2017
    Labeler - ARI&J Inc (694174441)
    Registrant - ARI&J Inc (694174441)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kolmar Korea Co., Ltd.689512611manufacture(71496-0001)
    Establishment
    NameAddressID/FEIBusiness Operations
    ARI&J Inc694174441label(71496-0001) , pack(71496-0001)
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