Label: TUMS ULTRA- calcium carbonate tablet, chewable

  • NDC Code(s): 0135-0553-01
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated February 26, 2025

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  • Active ingredient (per tablet)

    Calcium carbonate 1000 mg

  • Purpose

    Antacid

  • Uses

    relieves

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

    Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product

    •
    do not take more than 7 tablets in 24 hours
    •
    if pregnant do not take more than 5 tablets in 24 hours
    •
    do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor

    Keep out of reach of children.

  • Directions

    •
    adults and children 12 years of age and over: chew 2-3 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing.
    •
    do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
  • Other information

    •
    each tablet contains: elemental calcium 400 mg, magnesium 10 mg
    •
    store below 30°C (86°F)
    •
    contains FD&C Yellow No. 5 (tartrazine) as a color additive
  • Inactive ingredients

    corn starch, crospovidone, dextrose, FD&C red #40 lake, FD&C yellow #5 (tartrazine) lake, FD&C yellow #6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc

  • Questions?

    1-800-897-7535

  • Additional Information

    Safety sealed – Do not use if printed inner seal beneath cap is missing or broken.

    Gluten-Free

  • Principal Display Panel

    GOES TO WORK IN SECONDS!

    CALCIUM CARBONATE
    TUMS
    ANTACID

    Tropical
    Fruit

    72 CHEWABLE TABLETS

    ULTRA
    STRENGTH 1000

    Tums Ultra Strength Tropical Fruit 1000 mg 72 count
  • INGREDIENTS AND APPEARANCE
    TUMS  ULTRA
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0553
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorWHITE (Off-white) , YELLOW, ORANGE, REDScoreno score
    ShapeROUNDSize19mm
    FlavorTROPICAL FRUIT PUNCH, STRAWBERRY (Strawberry-banana) , PINEAPPLE (Pineapple-orange) , ORANGE (Mandarin orange) Imprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0553-0172 in 1 BOTTLE; Type 0: Not a Combination Product03/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00103/01/2023
    Labeler - Haleon US Holdings LLC (079944263)
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