Label: CHEEE GOLD PLUS TOOTH- silica, tocopheryl acetate paste, dentifrice

  • 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 July 7, 2020

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  • ACTIVE INGREDIENTS

    Silica 6.0%
    Tocopheryl Acetate 0.1%

  • INACTIVE INGREDIENTS

    SORBITOL, WATER, HYDRATED SILICA, PEG-32, SODIUM LAURYL SULFATE, CELLULOSE GUM, SODIUM METAPHOSPHATE, TITANIUM DIOXIDE, MENTHA PIPERITA(PEPPERMINT)OIL, CITRUS LIMON(LEMON)FRUIT OIL, XYLITOL, SODIUM SACCHARIN, PETERSONII OIL

  • PURPOSE

    Antiplaque
    Prevents gingivitis and periodontitis

  • WARNINGS

    Do not swallow, Rinse mouth after use. Stop use and consult a dentist or a doctor if anomalies occur in the mouth or on the gums after use. For children under 6 years use a pea-sized amount per use and supervise brushing to minimize swallowing. If more than used for brushing is swallowed by children under 6 years, consult a doctor or a dentist immediately. Keep out of reach of children under 6 years of age.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children under 6 years of age.

  • Uses

    Helps to protect against cavity and gingivitis inducing bacteria, as well as halitosis.

  • Directions

    Apply product onto a toothbrush and brush teeth. Use a smaller amount than other toothpaste for children or those more sensitive to taste. Keep the lid closed after each use. Brush teeth for 3 minutes or longer with Cheee Gold Toothpaste for better results.

  • Other Information

    Keep in airtight container in room temperature(1~30°C).

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of tube

  • INGREDIENTS AND APPEARANCE
    CHEEE GOLD PLUS TOOTH 
    silica, tocopheryl acetate paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79428-010
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (SILICON DIOXIDE - UNII:ETJ7Z6XBU4) SILICON DIOXIDE7.8 g  in 130 g
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0) (.ALPHA.-TOCOPHEROL - UNII:H4N855PNZ1) .ALPHA.-TOCOPHEROL ACETATE0.13 g  in 130 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79428-010-021 in 1 CARTON07/01/2020
    1NDC:79428-010-01130 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2020
    Labeler - Nature Plus (688361245)
    Registrant - Nature Plus (688361245)
    Establishment
    NameAddressID/FEIBusiness Operations
    KMPHARMACEUTICAL Co.,Ltd.688679158manufacture(79428-010)