Label: EQUATE SCULPTED WHITE TP EQUATE SCULPTED WHITE TP- sodium fluoride paste, dentifrice

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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

View All Sections
  • ACTIVE INGREDIENT

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

  • INACTIVE INGREDIENT

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

  • PURPOSE

    Anticavity

  • INDICATIONS & USAGE

    aids in the prevention of dental cavities

  • WARNINGS

    Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children under 6 years of age. If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    adults and children 2 years of age and older: brush teeth thoroughly, preferably after each meal or at least twice per day, or as directed by a dentist or doctor • instruct children under 6 years of age in good brushing habits (to minimize swallowing) • supervise children as necessary until capable of using without supervision • children under 2 years of age: Consult a dentist or doctor

  • PRINCIPAL DISPLAY PANEL

    2821079R1

  • INGREDIENTS AND APPEARANCE
    EQUATE SCULPTED WHITE TP  EQUATE SCULPTED WHITE TP
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:79903-282
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION0.15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    SORBITOL (UNII: 506T60A25R)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    MICA (UNII: V8A1AW0880)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    Product Characteristics
    Colorblue (light blue to green, with silver flecks) Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:79903-282-871 in 1 CARTON12/18/2024
    1107 g in 1 CARTON; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02212/18/2024
    Labeler - Walmart (051957769)
    Registrant - Lornamead (080046418)
    Establishment
    NameAddressID/FEIBusiness Operations
    Lornamead080046418manufacture(79903-282) , pack(79903-282)
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!