Label: BURTS BEES COMPLETE MULTI-CARE- sodium fluoride paste, dentifrice

  • NDC Code(s): 69423-835-14
  • Packager: Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 27, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium fluoride 0.243% (0.13% w/v fluoride ion)

  • Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • Warnings

    Keep out of reach of children under 6 yrs of age.If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • 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
    • do not swallow
    • to minimize swallowing use a pea-sized amount in children under 6
    • supervise children’s brushing until good habits are established
    • children under 2 yrs.: ask a dentist
  • Inactive ingredients

    glycerin, water, hydrated silica, flavor*, sodium
    lauryl glucose carboxylate, xanthan gum, lauryl glucoside, carrageenan,
    stevia rebaudiana extract, titanium dioxide

  • Questions?

    1-855-248-5352

  • SPL UNCLASSIFIED SECTION

    *Peppermint Oil and other Natural Flavor

  • SPL UNCLASSIFIED SECTION

    DISTR. BY SUNFLOWER DISTRIBUTING
    LLC, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 133 g tube in carton

    BURT'S

    BEES®

    Complete

    Multi-Care

    FLUORIDE

    Toothpaste

    Prevents Cavities

    Deep Cleans

    Freshens Breath

    6 Benefits

    Gently Whitens

    Removes Stains

    Strengthens Enamel
    ADA

    Accepeted

    American

    Dental

    Association

    Natural Peppermint

    NOT TESTE4D ON ANIMALS

    Made without SLS,

    artificial flavors & sweetners

    NET WT 4.7 OZ (133 g)

    Label

  • INGREDIENTS AND APPEARANCE
    BURTS BEES  COMPLETE MULTI-CARE
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-835
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.3 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEVIA REBAUDIANA WHOLE (UNII: 6U422Y08O2)  
    SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-835-143 in 1 CELLO PACK01/01/2020
    11 in 1 CARTON
    1133 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/01/2020
    Labeler - Procter & Gamble Manufacturing Company (004238200)
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