Label: HANDY SOLUTIONS CREST COMPLETE MULTI-BENEFIT WHITENING PLUS SCOPE- sodium fluoride paste, dentifrice

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

Drug Label Information

Updated April 15, 2024

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  • Handy Solutions Crest Complete MULTI-BENEFIT WHITENING plus Scope


  • Active ingredient

    Sodium fluoride 0.243%

  • Purpose

    Anti-Cavity toothpaste

  • Use

    helps protect against cavities

  • Warnings


    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. and 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 years : ask a dentist
  • Inactive ingredients

    Sorbitol, water, hydrated silica, disodium pyrophosphate, sodium lauryl sulfate, flavor, sodium hydroxide, alcohol (0.7%), xanthan gum, sodium saccharin, glycerin, carbomer, cellulose gum, polysorbate 80, sodium benzoate, cetylpyridinium chloride, benzoic acid, titanium dioxide, blue 1, yellow 5

  • Questions or comments?

    call toll-free 1-800-492-7378

  • PDP

    129803129159129804

  • INGREDIENTS AND APPEARANCE
    HANDY SOLUTIONS CREST COMPLETE MULTI-BENEFIT WHITENING PLUS SCOPE 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67751-095(NDC:58933-020)
    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
    SORBITOL (UNII: 506T60A25R)  
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    ALCOHOL (UNII: 3K9958V90M)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)  
    BENZOIC ACID (UNII: 8SKN0B0MIM)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorPEPPERMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:67751-095-011 in 1 PACKAGE08/21/2013
    124 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:67751-095-031 in 1 PACKAGE08/21/2013
    243 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:67751-095-041 in 1 PACKAGE08/21/2013
    3113 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02108/16/2013
    Labeler - Navajo Manufacturing Company Inc (091917799)
    Establishment
    NameAddressID/FEIBusiness Operations
    THE PROCTER & GAMBLE MANUFACTURING COMPANY005279245manufacture(67751-095)
    Establishment
    NameAddressID/FEIBusiness Operations
    Navajo Manufacturing Company Inc136941411relabel(67751-095) , repack(67751-095)
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