Label: BURTS BEES KIDS STRAWBERRY SPLASH- sodium fluoride paste, dentifrice

  • NDC Code(s): 69423-819-47
  • Packager: Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 1, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

    Sodium fluoride 0.243% (0.14% 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

    *Natural Flavor



  • SPL UNCLASSIFIED SECTION

    DISTR. BY SUNFLOWER DISTRIBUTING
    LLC, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 119 g tube

    IMPROVED FORMULA

    burt's

    bees®

    KIDS

    fluoride

    toothpaste

    STRARBERRY

    SPLASH

    PREVENTS CAVITIES
    TASTES GREAT
    DYE-FREE

    ADA

    Accepted

    American

    Dental

    Association

    NOT TESTED ON ANIMALS

    NET WT 4.7 OZ (133 g)

    Label

  • INGREDIENTS AND APPEARANCE
    BURTS BEES KIDS  STRAWBERRY SPLASH
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-819
    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
    SODIUM LAURYL GLYCOL CARBOXYLATE (UNII: 8L0472VMYL)  
    CARRAGEENAN (UNII: 5C69YCD2YJ)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    STEVIA REBAUDIANA WHOLE (UNII: 6U422Y08O2)  
    SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)  
    LAURYL GLUCOSIDE (UNII: 76LN7P7UCU)  
    Product Characteristics
    ColorredScore    
    ShapeSize
    FlavorSTRAWBERRYImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-819-47133 g in 1 TUBE; Type 0: Not a Combination Product10/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02110/01/2023
    Labeler - Procter & Gamble Manufacturing Company (004238200)