Label: AIM CAVITY PROTECTION MULTI BENEFIT- sodium fluoride gel, dentifrice

  • NDC Code(s): 10237-633-22, 10237-633-45, 10237-633-55, 10237-633-60, view more
    10237-633-66, 10237-633-72
  • Packager: Church & Dwight Co., Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2025

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  • ACTIVE INGREDIENT

    Active ingredients 
    Sodium fluoride (0.24%)

  • PURPOSE

    Purpose
    Anticavity toothpaste

  • INDICATIONS & USAGE

    Use  aids in the prevention of dental decay

  • KEEP OUT OF REACH OF CHILDREN

    Warnings
    Keep out of reach of children under 6 years of age     .

  • WARNINGS

    If more than used for brushing is accidentally swallowed, get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Directions    do not swallow    supervise children as necessary until capable of using without supervision

    adults and children 2 years and older brush teeth thoroughly after meals or at least twice a day, or use as directed by a dentist or physician
    children under 6 years instruct in good brushing and rinsing habits (to minimize swallowing)
    children under 2 years ask a dentist or physician

  • INACTIVE INGREDIENT

    Inactive ingredients sorbitol, water, hydrated silica, PEG-8, sodium lauryl sulfate, SD alcohol 38-B, flavor, cellulose gum, sodium saccharin, blue 1, yellow 10.

  • QUESTIONS

    Questions or comments?  Call 1-800-786-5135 Monday-Friday 9am-5pm ET

  • Principal Display Panel

    Value Pack

    20%

    MORE

    Product

    on sizes up to 4.6 oz.

    ADA

    Accepted

    American

    Dental

    Association

    TAKE AIM AGAINST CAVITIES

    Aim

    CAVITY PROTECTION

    Ultra Mint

    Gel

    MULTI-BENEFIT

    Cleans

    Freshens

    Protects

    Anticavity Fluoride Gel Toothpaste

    NET WT. 5.5 OZ. (156g)

    AMFC-00093-01_70505178_DA1081102

  • INGREDIENTS AND APPEARANCE
    AIM CAVITY PROTECTION  MULTI BENEFIT
    sodium fluoride gel, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-633
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION2.4 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    PEG-8 STEARATE (UNII: 2P9L47VI5E)  
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    ALCOHOL (UNII: 3K9958V90M)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorgreenScore    
    ShapeSize
    FlavorMINT (Ultra Mint) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10237-633-601 in 1 CARTON08/01/201509/26/2019
    1170 g in 1 TUBE; Type 0: Not a Combination Product
    2NDC:10237-633-721 in 1 CARTON08/01/201509/26/2019
    2204 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:10237-633-221 in 1 CARTON08/01/201509/26/2019
    362 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:10237-633-551 in 1 CARTON08/01/2015
    4156 g in 1 TUBE; Type 0: Not a Combination Product
    5NDC:10237-633-661 in 1 CARTON08/01/201506/30/2025
    5187 g in 1 TUBE; Type 0: Not a Combination Product
    6NDC:10237-633-451 in 1 CARTON02/28/2022
    6127 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02103/01/2004
    Labeler - Church & Dwight Co., Inc. (001211952)
    Establishment
    NameAddressID/FEIBusiness Operations
    Church & Dwight Co., Inc.043690812manufacture(10237-633)
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