Label: CREST TARTAR PROTECTION- sodium fluoride paste, dentifrice

  • NDC Code(s): 58933-008-02, 58933-008-03, 58933-008-04, 58933-008-24, view more
    58933-008-57
  • Packager: Procter & Gamble Manufactura, S. de R.L. de C.V.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 6, 2024

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient

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

  • Purpose

    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. & 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, disodium pyrophosphate, sodium hydroxide, sodium lauryl sulfate, flavor, xanthan gum, sodium saccharin, carbomer, cellulose gum, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    Dist. by Procter & Gamble, Cincinnati, OH 45202

  • PRINCIPAL DISPLAY PANEL - 161 g Tube Carton

    HELPS PREVENT TARTAR & CAVITIES

    Crest®

    ADA

    Accepted


    American

    Dental

    Association ®

    FLUORIDE ANTICAVITY TOOTHPASTE

    NET WT 5.7 OZ (161 g)

    TARTAR

    PROTECTION

    Regular PasteTartar Protection

  • INGREDIENTS AND APPEARANCE
    CREST TARTAR PROTECTION 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58933-008
    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
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorCINNAMONImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58933-008-021 in 1 CARTON11/06/1992
    182 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:58933-008-031 in 1 CARTON11/06/1992
    2130 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:58933-008-041 in 1 CARTON11/06/1992
    3181 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:58933-008-571 in 1 CARTON09/10/2021
    4161 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:58933-008-241 in 1 CARTON09/10/2021
    568 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02111/06/1992
    Labeler - Procter & Gamble Manufactura, S. de R.L. de C.V. (812807550)