Label: KIDS CREST CAVITY PROTECTION SPARKLE FUN- sodium fluoride paste, dentifrice

  • NDC Code(s): 58933-049-01, 58933-049-06, 58933-049-13, 58933-049-22, view more
    58933-049-46, 58933-049-62
  • Packager: Procter & Gamble Manufactura, S. de R.L. de C.V.
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 6, 2024

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  • Drug Facts

  • Active ingredient

    Sodium fluoride 0.243%
    (0.15% w/v fluoride ion)

  • Purpose

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • WARNINGS

    Warning

    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

    sorbitol, water, hydrated silica, sodium lauryl sulfate, trisodium phosphate, sodium phosphate, cellulose gum, flavor, sodium saccharin, carbomer, mica, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    MADE IN MEXICO
    DIST. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL - 76.5 g Tube in Carton Label

    KID'S
    CREST     ®

    CAVITY
    PROTECTION

    SPARKLE FUN


    ADA
    Accepted
    American
    Dental
    Association ®

    FLUORIDE
    ANTICAVITY
    TOOTHPASTE

    NET WT 2.7 OZ (76.5 g)

    049

  • INGREDIENTS AND APPEARANCE
    KIDS CREST CAVITY PROTECTION  SPARKLE FUN
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58933-049
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.5 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58933-049-06170 g in 1 TUBE; Type 0: Not a Combination Product09/05/200211/30/2018
    2NDC:58933-049-0124 g in 1 TUBE; Type 0: Not a Combination Product09/05/2002
    3NDC:58933-049-221 in 1 CARTON11/01/2020
    362 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:58933-049-461 in 1 CARTON11/01/2020
    4130 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:58933-049-133 in 1 CELLO PACK11/01/2020
    5130 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:58933-049-6262 g in 1 TUBE; Type 0: Not a Combination Product09/05/2002
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02109/05/2002
    Labeler - Procter & Gamble Manufactura, S. de R.L. de C.V. (812807550)
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