Label: A.H.C. COLLAGEN TONER- adenosine 0.04% 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 August 6, 2013

If you are a consumer or patient please visit this version.

  • Drug Facts
  • ACTIVE INGREDIENT

     Active Ingredients  Purpose
     Adenosine 0.04%  Skin Protectant     

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  • Uses

    Help to improve skin natural health

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  • Warning

    For external use only

    Do not use

    on damage or broken skin

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  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of Children.

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  • INSTRUCTIONS FOR USE

    Apply small amount to a clean skin and massage gently with fingertips.

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  • DOSAGE & ADMINISTRATION

    Dosage: Small Amount

    Administration: apply to a clean skin and massage gently

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  • Inactive Ingredients

    WATER
    DIPROPYLENE GLYCOL
    BUTYLENE GLYCOL
    GLYCERIN
    UREA
    PEG-32 STEARATE
    CARBOMER 934
    TROLAMINE
    HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW)
    PHENOXYETHANOL
    ALOE VERA LEAF
    PONCIRUS TRIFOLIATA FRUIT
    ALLANTOIN
    COCETH-7 CARBOXYLIC ACID
    LAURYL GLYCOL HYDROXYPROPYL ETHER
    PEG-40 CASTOR OIL
    GLYCYRRHIZINATE DIPOTASSIUM
    HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)
    .ALPHA.-TOCOPHEROL ACETATE
    HYALURONATE SODIUM
    ORYZA SATIVA WHOLE
    TARAXACUM OFFICINALE ROOT
    CAMELLIA SINENSIS WHOLE
    CENTELLA ASIATICA
    POLYGALA TENUIFOLIA ROOT
    PLATYCODON GRANDIFLORUM ROOT
    EDETIC ACID
    SULISOBENZONE
    LAVANDULA ANGUSTIFOLIA WHOLE
    MONARDA DIDYMA LEAF
    MENTHA PIPERITA LEAF
    FREESIA ALBA FLOWER
    MATRICARIA CHAMOMILLA WHOLE
    ROSMARINUS OFFICINALIS FLOWER
    FD&C YELLOW NO. 6
    FD&C YELLOW NO. 5

    Fragnance

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  • PRINCIPAL DISPLAY PANEL - 120mL Bottle Carton
  • INGREDIENTS AND APPEARANCE
    A.H.C. COLLAGEN TONER 
    adenosine 0.04% liquid
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:58930-039
    Route of Administration TOPICAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE 48 mg  in 120 mL
    Inactive Ingredients
    Ingredient Name Strength
    WATER (UNII: 059QF0KO0R)  
    DIPROPYLENE GLYCOL (UNII: E107L85C40)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    UREA (UNII: 8W8T17847W)  
    PEG-32 STEARATE (UNII: 33GX5WQC0M)  
    CARBOMER 934 (UNII: Z135WT9208)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    HYDROLYSED MARINE COLLAGEN (ENZYMATIC; 2000 MW) (UNII: 2WID9OCG7P)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    PONCIRUS TRIFOLIATA FRUIT (UNII: 44445L49J2)  
    ALLANTOIN (UNII: 344S277G0Z)  
    COCETH-7 CARBOXYLIC ACID (UNII: 35KO064932)  
    LAURYL GLYCOL HYDROXYPROPYL ETHER (UNII: 4KDJ27EOJE)  
    PEG-40 CASTOR OIL (UNII: 4ERD2076EF)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ORYZA SATIVA WHOLE (UNII: 84IVV0906Z)  
    TARAXACUM OFFICINALE ROOT (UNII: 9DE5YCO0RU)  
    CAMELLIA SINENSIS WHOLE (UNII: C5M4585ZBZ)  
    CENTELLA ASIATICA (UNII: 7M867G6T1U)  
    POLYGALA TENUIFOLIA ROOT (UNII: 5S7W573MTU)  
    PLATYCODON GRANDIFLORUM ROOT (UNII: 2DF0NS0O2Z)  
    EDETIC ACID (UNII: 9G34HU7RV0)  
    SULISOBENZONE (UNII: 1W6L629B4K)  
    LAVANDULA ANGUSTIFOLIA WHOLE (UNII: 51217XIL5L)  
    MONARDA DIDYMA LEAF (UNII: JY15982UBB)  
    MENTHA PIPERITA LEAF (UNII: A389O33LX6)  
    FREESIA ALBA FLOWER (UNII: 33X293N6JT)  
    MATRICARIA CHAMOMILLA WHOLE (UNII: 2Z4LRR776S)  
    ROSMARINUS OFFICINALIS FLOWER (UNII: NR1A27F29O)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:58930-039-01 1 in 1 CARTON
    1 120 mL in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 08/15/2013
    Labeler - Carver Korea Co.,Ltd (688442290)
    Registrant - Jemian USA Inc. (078822273)
    Establishment
    Name Address ID/FEI Business Operations
    Eyesome Co.,Ltd. 557795360 manufacture(58930-039)
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