Label: NOBLE G PLUS - xylitol paste, dentifrice 

  • Label RSS
  • NDC Code(s): 60319-3001-1
  • Packager: Hankuk Bowonbio Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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 11/12

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

  • ACTIVE INGREDIENT

    active ingredient:  xylitol
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  • INACTIVE INGREDIENT

    silicone dioxide, sodium monofluorophosphate, hydrated silicone dioxide, d-sorbitol, carboxymethylcellulose sodium, sodium lauryl sulfate, sodium saccharin, gold leaf, green tea extract, polyethylene glycol 1500, L-menthol, hydroxyapatite, chitosan, stearic acid, polysorbate 80, water
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  • PURPOSE

    whiten and strong teeth
    removal of bad breath
    prevention of gingivitis and periodontitis
    prevention of periodontal diseases and gum diseases
    removal of dental plaque

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  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children
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  • INDICATIONS & USAGE

    apply Proper Amount of the toothpaste on the tooth.

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  • WARNINGS

    ■ For tooth only.
    ■ Avoid contact with eyes.
    ■ Do not swallow. If swallowed, get medical help.

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  • DOSAGE & ADMINISTRATION

    brush your teeth by putting appropriate amount of tooth paste
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  • INGREDIENTS AND APPEARANCE
    NOBLE G PLUS 
    xylitol paste, dentifrice
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:60319-3001
    Route of Administration DENTAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    XYLITOL (XYLITOL) XYLITOL 0.7 g  in 100 g
    Inactive Ingredients
    Ingredient Name Strength
    WATER  
    SILICON DIOXIDE  
    SODIUM MONOFLUOROPHOSPHATE  
    HYDRATED SILICA  
    SORBITOL  
    CARBOXYMETHYLCELLULOSE SODIUM  
    SODIUM LAURYL SULFATE  
    SACCHARIN SODIUM ANHYDROUS  
    GOLD  
    GREEN TEA LEAF  
    POLYETHYLENE GLYCOL 1500  
    LEVOMENTHOL  
    TRIBASIC CALCIUM PHOSPHATE  
    CHITOSAN OLIGOSACCHARIDE  
    ISOSTEARIC ACID  
    POLYSORBATE 80  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:60319-3001-1 130 g in 1 TUBE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved drug other 11/30/2012
    Labeler - Hankuk Bowonbio Co., Ltd (690045133)
    Registrant - Hankuk Bowonbio Co., Ltd (690045133)
    Establishment
    Name Address ID/FEI Business Operations
    Hankuk Bowonbio Co., Ltd 690045133 manufacture(60319-3001)
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