Label: AVON WHITENING ESSENTIALS BLANC CHARCOAL FRESH MINT- sodium fluoride paste, dentifrice

  • NDC Code(s): 43136-903-01
  • Packager: Tai Guk Pharm. Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2025

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  • Drug Facts

    Drug Facts

  • Active Ingredient

    Sodium fluoride 0.243% (0.16% w/v fluoride ion)

  • Purpose

    Anticavity

  • Use

    helps protect against cavities

  • Warnings

    Warnings

    Keep out of reach of children.

    Keep out of reach of children under 6 years of age. Do not swallow. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away. If an allergic reaction develops, discontinue to use immediately.

  • Directions

    Adults and children 6 years and olderBrush teeth thoroughly after each means or at least twice a day, or as directed by a dentist and physician. Do not swallow.
    Children between 6 and 12 yearsTo minimize swallowing, use a pea-sized amount and supervise children's brushing and rinsing until good habits are established.
    Children under 6 yearsAsk a dentist or physician.

  • Inactive Ingredients

    glycerin, hydrated silica, sodium hexametaphosphate, water, PEG-6, flavor, trisodium phosphate, sodium lauryl sulfate, carrageenan, cocamidopropyl betaine, sodium saccharin, sucralose, xanthan gum, titanium dioxide, mica, charcoal powder, citru limon(lemon) fruit extract, sodium chloride

  • QUESTIONS

    1-800-FOR-AVON

    www.avon.com

  • Principal Display Panel - 20 g Tube Carton

    AVON

    Whitening Essentials

    FLUORIDE TOOTHPASTE

    CAVITY PROTECTION

    HELPS WHITEN TEETH - REMOVES SURFACE STAINS

    BLANC CHARCOAL

    FRESH MINT

    NET WT 0.7 oz (20 g)

    Avon WETPFM20

  • INGREDIENTS AND APPEARANCE
    AVON WHITENING ESSENTIALS  BLANC CHARCOAL FRESH MINT
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43136-903
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.6 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    HEXASODIUM HEXAMETAPHOSPHATE (UNII: N40N91DW96)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    POLYETHYLENE GLYCOL 300 (UNII: 5655G9Y8AQ)  
    SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    MICA (UNII: V8A1AW0880)  
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorMINT (Fresh) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43136-903-011 in 1 CARTON12/25/2019
    120 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02112/25/2019
    Labeler - Tai Guk Pharm. Co., Ltd. (689060246)
    Establishment
    NameAddressID/FEIBusiness Operations
    Tai Guk Pharma. Co., Ltd.689060246manufacture(43136-903)
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