Label: CREST 3D WHITE STAIN ERASER ICY CLEAN MINT- sodium fluoride paste, dentifrice

  • NDC Code(s): 69423-773-31, 69423-773-44, 69423-773-62, 69423-773-63
  • Packager: The Procter & Gamble Manufacturing Company
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 12, 2023

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

View All Sections
  • Drug Facts

    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

    water, sorbitol, hydrated silica, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, cellulose gum, sodium saccharin, carbomer, polysorbate 80, mica, titanium dioxide, blue 1

  • Questions?

    1-800-492-7378

  • SPL UNCLASSIFIED SECTION

    DISTR. BY PROCTER & GAMBLE, CINCINNATI, OH 45202

  • Crest 3D White Stain Eraser Icy Clean Mint

    Crest

    3D White

    Fluoride Anticavity Toothpaste

    Enamel Safe Whitening

    NET WT 3.1 OZ (87 g)

    Stain Eraser

    Icy Clean Mint

    Removes up to 80% of surface stains*

    Coffee Soda Tea Wine

    artwork

  • INGREDIENTS AND APPEARANCE
    CREST 3D WHITE  STAIN ERASER ICY CLEAN MINT
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-773
    Route of AdministrationORAL
    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
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SORBITOL (UNII: 506T60A25R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    WATER (UNII: 059QF0KO0R)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    MICA (UNII: V8A1AW0880)  
    Product Characteristics
    ColorblueScore    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-773-311 in 1 CARTON07/09/2021
    187 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:69423-773-622 in 1 CELLO PACK07/09/2021
    21 in 1 CARTON
    287 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:69423-773-633 in 1 CELLO PACK07/09/2021
    31 in 1 CARTON
    387 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:69423-773-441 in 1 CARTON01/01/2023
    4124 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02107/09/2019
    Labeler - The Procter & Gamble Manufacturing Company (004238200)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!