Label: ROLAIDS ULTRA STRENGTH MINT- calcium carbonate, magnesium hydroxide tablet, chewable

  • NDC Code(s): 69423-828-10, 69423-828-72
  • Packager: THE PROCTER & GAMBLE MANUFACTURING COMPANY
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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

  • SPL UNCLASSIFIED SECTION

    ULTRASTRENGTHRolaids Mint 72 Chewable Tablets

    Drug Facts

  • Active ingredients

    (in each tablet)
    Calcium carbonate USP 1000 mg
    Magnesium hydroxide USP 200 mg

  • Purposes

    Antacid

    Antacid

  • Uses

    relieves:

    • heartburn
    • sour stomach
    • acid indigestion
    • upset stomach associated with these symptoms
  • Warnings

    Ask a doctor or pharmacist before use if you

    • are now taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product

    • do not take more than 7 tablets in a 24-hour period
    • do not use the maximum dosage for more than 2 weeks

    Keep out of reach of children.

  • Directions

    • chew 2-3 tablets as symptoms occur, or as directed by a doctor
  • Other information

    each tablet contains:calcium 400 mg, magnesium 85 mg

  • Inactive ingredients

    dextrose, flavor, magnesium stearate, maltodextrin, silicon dioxide, stearic acid, sucralose, sucrose

  • Questions?

    1-833-372-2729

  • Tamper Evident

    Do not use if inner foil seal on bottle is broken or missing

  • SPL UNCLASSIFIED SECTION

    DIST. BY: PROCTER & GAMBLE, CINCINNATI, OH 45202

  • PRINCIPAL DISPLAY PANEL

    ULTRASTRENGTH
    Rolaids ®
    ANTACID/CALCIUM & MAGNESIUM SUPPLEMENT
    Goes to Work Instantly

    Mint

    Naturally and Artificially flavored

    72 Chewable Tablets

    828

  • INGREDIENTS AND APPEARANCE
    ROLAIDS ULTRA STRENGTH  MINT
    calcium carbonate, magnesium hydroxide tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-828
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S) (MAGNESIUM CATION - UNII:T6V3LHY838) MAGNESIUM HYDROXIDE200 mg
    Inactive Ingredients
    Ingredient NameStrength
    DEXTROSE (UNII: IY9XDZ35W2)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SUCROSE (UNII: C151H8M554)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize19mm
    FlavorMINTImprint Code R;U
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69423-828-1010 in 1 PACKAGE; Type 0: Not a Combination Product01/30/2024
    2NDC:69423-828-7272 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00101/30/2024
    Labeler - THE PROCTER & GAMBLE MANUFACTURING COMPANY (004238200)