Label: TOURCIA NUTRI TONER- allantoin cream

  • NDC Code(s): 43275-190-01
  • Packager: NUGA MEDICAL CO., LTD.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated 02/13

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENT: ALLANTOIN 0.5%

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS:
    Water, Glycereth-26, Glycerin, Dipropylene Glycol, Alcohol Denat., PEG/PPG-17/6 Copolymer, Bis-PEG-18 Methyl Ether Dimethyl Silane, Phenoxyethanol, PEG-60 Hydrogenated Castor Oil, Methylparaben, Arginine, Carbomer, Adenosine, Fragrance(Parfum), Disodium EDTA, Propylene Glycol, Butylene Glycol, Acacia Seyal Gum Extract, PVP, Potassium Sorbate, Sodium Cocoyl Alaninate, Tourmaline, Dipeptide Diaminobutyroyl Benzylamide Diacetate, Butylparaben, Ethylparaben, Isobutylparaben, Propylparaben, Hydrolyzed Myrtus Communis Leaf Extract, Fullerenes, Gelatin, Ethylhexylglycerin

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  • PURPOSE

    PURPOSE: Wrinkle Functional cosmetics (Skin Protectant)

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  • WARNINGS

    WARNINGS:
    For external use only
    Do Not Use - On wounds or damaged skin
    When using this product:
    - do not use other than directed
    Stop use - If allergic reaction or irritation occurs

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  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

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  • INDICATIONS AND USAGE

    HOW TO USE:
    Take a proper amount of this product and apply it evenly to the skin after washing your face.

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  • DOSAGE AND ADMINISTRATION

    HOW TO USE:
    Take a proper amount of this product and apply it evenly to the skin after washing your face.

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  • PACKAGE LABEL. PRINCIPAL DISPLAY PANEL
  • INGREDIENTS AND APPEARANCE
    TOURCIA NUTRI TONER 
    allantoin cream
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:43275-190
    Route of Administration TOPICAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    ALLANTOIN (ALLANTOIN) ALLANTOIN 0.75 mg  in 150 mL
    Inactive Ingredients
    Ingredient Name Strength
    Water  
    Glycereth-26  
    Glycerin  
    Dipropylene Glycol  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:43275-190-01 150 mL in 1 CARTON
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part347 10/01/2012
    Labeler - NUGA MEDICAL CO., LTD. (690034673)
    Registrant - NUGA MEDICAL CO., LTD. (690034673)
    Establishment
    Name Address ID/FEI Business Operations
    NUGA MEDICAL CO., LTD. 690034673 manufacture(43275-190)
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