Label: KIDS CREST ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING- stannous fluoride paste, dentifrice

  • NDC Code(s): 69423-896-04, 69423-896-29, 69423-896-42, 69423-896-85
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 13, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Drug Facts

    Active ingredient

    Sodium monofluorophosphate 0.834% (0.15% w/v fluoride ion)

  • Purposes

    Anticavity toothpaste

  • Use

    helps protect against cavities

  • 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. of age and older: brush teeth thoroughly after meals or at least twice a day or as directed by a dentist

    • do not swallow

    • to minimize swallowing use a pea-sized amount in children under 6 yrs.

    • supervise children's brushing until good habits are established

    • children under 2 yrs.: ask a dentist

  • INACTIVE INGREDIENT

    sorbitol, water, hydrated silica, sodium lauryl sulfate, cellulose gum, flavor, sodium phosphate, trisodium phosphate, mannitol, sodium saccharin, carbomer, silica, titanium dioxide, red 30 lake, blue 1

  • QUESTIONS

    Questions? 1-800-594-4158

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE,

    CINCINNATI, OH 45202

  • KIDS Crest Advanced Color Changing

    KIDS BRUSH UP TO 2X LONGER

    3+ YRS

    KID'S Crest ADVANCED

    FLUORIDE ANTICAVITY TOOTHPASTE

    COLOR CHANGING

    I CHANGE BLUE TO PINK WHEN CLEANING

    BUBBLEGUM

    NET WT 4.2 OZ (119 g)

    Kids Color Change

  • INGREDIENTS AND APPEARANCE
    KIDS CREST  ADVANCED FLUORIDE ANTICAVITY COLOR CHANGING
    stannous fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-896
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION1.6 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    SORBITOL (UNII: 506T60A25R)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SODIUM PHOSPHATE (UNII: SE337SVY37)  
    SODIUM PHOSPHATE, TRIBASIC, ANHYDROUS (UNII: SX01TZO3QZ)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    MANNITOL (UNII: 3OWL53L36A)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorBUBBLE GUMImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-896-8524 g in 1 TUBE; Type 0: Not a Combination Product01/01/2023
    2NDC:69423-896-291 in 1 CARTON01/01/2023
    282 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69423-896-421 in 1 CARTON01/01/2023
    3119 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69423-896-044 in 1 CARTON01/01/2023
    4119 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02101/01/2023
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
    Establishment
    NameAddressID/FEIBusiness Operations
    Procter & Gamble Manufacturing México, S. de R.L. de C.V.812807550manufacture(69423-896)