Label: BAMBOO SALT EUNGANGGO JOOK YEOM TOOTHPASTE - silicon dioxide , sodium fluoride, aminocaproic acid, glycyrrhizinate dipotassium, ursodiol, curcuma xanthorrhiza oil and sea salt paste

  • NDC Code(s): 53208-459-01, 53208-459-02
  • Packager: LG Household and Healthcare, Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not 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 06/10

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

  • ACTIVE INGREDIENT

    SILICON DIOXIDE  20 %

    SODIUM FLUORIDE 0.22 %

    AMINOCAPROIC ACID 0.05 %

    GLYCYRRHIZINATE DIPOTASSIUM 0.04 %

    URSODIOL 0.02 %

    SEA SALT 3 %





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  • DOSAGE & ADMINISTRATION

    Direction: Suggested brushing your teeth with proper amount for at least two times per day or following dentist / doctor's instruction.

    Children between two to six should use about two to six should use about a size of a pea and should be supervised by adults while using.


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  • WARNINGS AND PRECAUTIONS

    This product is for brushing teeth only and uneatable. If a rash occurs, stop using this product and consult a doctor or dentist.

    If it comes in contact with eyes, cleanse off immediately and consult a doctor. Store this product away from children and supervise them while using.

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  • PRINCIPAL DISPLAY PANEL

    BAMBOO SALT

    Eunganggo Toothpaste

    Bamboo Toothpaste

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  • INGREDIENTS AND APPEARANCE
    BAMBOO SALT EUNGANGGO JOOK YEOM TOOTHPASTE 
    silicon dioxide , sodium fluoride, aminocaproic acid, glycyrrhizinate dipotassium, curcuma xanthorrhiza oil, sea salt paste
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:53208-459
    Route of Administration DENTAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    SILICON DIOXIDE (SILICON DIOXIDE ) SILICON DIOXIDE 20 g  in 100 g
    SODIUM FLUORIDE (Fluoride Ion) SODIUM FLUORIDE 0.22 g  in 100 g
    AMINOCAPROIC ACID (AMINOCAPROIC ACID) AMINOCAPROIC ACID 0.05 g  in 100 g
    GLYCYRRHIZINATE DIPOTASSIUM (GLYCYRRHIZINATE DIPOTASSIUM) GLYCYRRHIZINATE DIPOTASSIUM 0.04 g  in 100 g
    URSODIOL (URSODIOL) URSODIOL 0.02 g  in 100 g
    Curcuma xanthorrhiza oil (Curcuma xanthorrhiza oil) Curcuma xanthorrhiza oil 0.025 g  in 100 g
    SEA SALT (SEA SALT ) SEA SALT 3 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    SORBITOL  
    Polyethylene Glycol 300  
    XANTHAN GUM  
    Poloxamer 407  
    Sodium Lauryl Sulfate  
    Sodium Bisulfite  
    Titanium Dioxide  
    WATER  
    Peppermint  
    FD&C BLUE NO. 1  
    D&C YELLOW NO. 10  
    METHYLPARABEN  
    SACCHARIN SODIUM  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:53208-459-02 1 in 1 CARTON
    1 NDC:53208-459-01 170 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph not final part355 05/25/2010
    Labeler - LG Household and Healthcare, Inc. (688276187)
    Registrant - LG Household and Healthcare, Inc. (688276187)
    Establishment
    Name Address ID/FEI Business Operations
    LG Household and Healthcare, Inc. 688276187 manufacture
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