Label: ARM AND HAMMER- sodium fluoride paste, dentifrice

  • NDC Code(s): 10237-679-06
  • Packager: Church & Dwight Co., Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 1, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Sodium fluoride 0.24% (0.17% w/v fluoride ion)

  • Purpose

    Anticavity

  • Use

    aids in the prevention of dental decay

  • WARNINGS

    Warnings

    Do not use if irritation occurs and persists

    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.

  • Directions

    • do not swallow • supervise children as necessary until capable of using without supervision • rinse away toothpaste residue thoroughly after brushing

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

  • Inactive ingredients

    water, sodium bicarbonate, sorbitol, hydrated silica, glycerin, tetrasodium pyrophosphate, flavor, sodium saccharin, cellulose gum, sodium lauroyl sarcosinate, sodium lauryl sulfate, titanium dioxide

  • Questions or comments?

    Call 1-800-786-5135 Mon-Fri, 9am - 5 pm ET or visit www.myoralcare.com

  • PRINCIPAL DISPLAY PANEL

    Anticavity Fluoride Toothpaste

    ARM & HAMMER

    THE STANDARD OF PURITY

    CAVITY PROTECTION

    helps remove surface stains and plaque

    Classic Mint

    NET WT 6.0 OZ (170g)

    AH Cavity Protection TP Carton

  • INGREDIENTS AND APPEARANCE
    ARM AND HAMMER 
    sodium fluoride paste, dentifrice
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10237-679
    Route of AdministrationDENTAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    SODIUM FLUORIDE (UNII: 8ZYQ1474W7) (FLUORIDE ION - UNII:Q80VPU408O) SODIUM FLUORIDE2.4 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
    SODIUM LAUROYL SARCOSINATE (UNII: 632GS99618)  
    SODIUM PYROPHOSPHATE (UNII: O352864B8Z)  
    WATER (UNII: 059QF0KO0R)  
    SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    SORBITOL (UNII: 506T60A25R)  
    HYDRATED SILICA (UNII: Y6O7T4G8P9)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    Product Characteristics
    Color    Score    
    ShapeSize
    FlavorMINTImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10237-679-061 in 1 CARTON06/01/2026
    1170 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02106/01/2026
    Labeler - Church & Dwight Co., Inc. (001211952)
    Establishment
    NameAddressID/FEIBusiness Operations
    Church & Dwight Co., Inc.043690812manufacture(10237-679)
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