Label: FLAVON CHARCOAL MINT TOOTH- calcium carbonate, allantoin powder, dentifrice

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated July 25, 2020

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  • ACTIVE INGREDIENT

    Calcium Carbonate 45.0%
    Allantoin 1.0%

  • PURPOSE

    Anti-plaque
    Anti-gingivitis, Anti-Periodontitis

  • Uses

    Aids in the removal of plaque and prevention gingivitis and periodontitis.

  • WARNINGS

    Keep out of the reach of children under 6 years of age.
    If you accidentally swallow more than used for brushing, seek professional help or contact a poison control center immediately.

  • KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    Adults and children 2 yrs. older: Brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician. Do not swallow.
    Children under 6 yrs.: To minimize swallowing, use a pea-sized amount and supervise brushing until good habits are established.
    Children under 2 yrs.: Ask a dentist or physician.

  • Other Information

    Store at room temperature

  • QUESTIONS

    Visit www.beauti-science.com/whitelabs/en

  • INACTIVE INGREDIENTS

    Sorbitol, Sodium Bicarbonate, Sodium Lauryl Sulfate, Xylitol, Xanthan Gum, Mint Flavor, Menthol, Mentha Piperita Oil, Stevioside, Charcoal Powder, Ascorbic Acid

  • PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

    Image of carton

  • INGREDIENTS AND APPEARANCE
    FLAVON CHARCOAL MINT TOOTH 
    calcium carbonate, allantoin powder, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73660-002
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Calcium Carbonate (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION45.0 g  in 100 g
    Allantoin (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z) Allantoin1.0 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    Sorbitol (UNII: 506T60A25R)  
    Sodium Bicarbonate (UNII: 8MDF5V39QO)  
    Sodium Lauryl Sulfate (UNII: 368GB5141J)  
    Xylitol (UNII: VCQ006KQ1E)  
    Xanthan Gum (UNII: TTV12P4NEE)  
    Menthol (UNII: L7T10EIP3A)  
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    Stevioside (UNII: 0YON5MXJ9P)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    ASCORBIC ACID (UNII: PQ6CK8PD0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73660-002-021 in 1 CARTON07/01/2020
    1NDC:73660-002-0150 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/01/2020
    Labeler - BS and Co. Ltd (689513606)
    Registrant - BS and Co. Ltd (689513606)
    Establishment
    NameAddressID/FEIBusiness Operations
    BIOSTECH CO., LTD.687294330manufacture(73660-002)
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