Label: TUMS ULTRA- calcium carbonate tablet, chewable

  • NDC Code(s): 0135-0235-01, 0135-0235-02
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 4, 2024

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  • Active ingredient (in each 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
    • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor
  • Other information

    • each tablet contains:elemental calcium 400mg, magnesium 10 mg
    • store below 30 oC (86 oF)
  • Inactive ingredients

    corn starch, crospovidone, dextrose, flavor, magnesium stearate, maltodextrin, sucrose, talc

  • Questions?

    1-800-897-7535

  • Principal Display Panel

    NDC 0135-0235-01

    TUMS

    CALCIUM CARBONATE

    ANTACID

    GOES TO WORK IN SECONDS!

    Peppermint

    ULTRASTRENGTH1000

    72CHEWABLETABLETS

    DO NOT USE IF PRINTED SEAL UNDER CAP IS TORN OR MISSING.

    Dist. by: GSK CH,Warren, NJ 07059

    ©2021 GSK or licensor.

    1001218 (Front Label)

    1001219 (Back Label)

    TUMS Ultra Peppermint 72 ct front label
  • INGREDIENTS AND APPEARANCE
    TUMS   ULTRA
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-0235
    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
    CORN STARCH 3-E-DODECENYL SUCCINIC ANHYDRIDE MODIFIED (UNII: QG4MW19XYX)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize19mm
    FlavorPEPPERMINTImprint Code TUMS
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-0235-0172 in 1 BOTTLE; Type 0: Not a Combination Product06/21/2021
    2NDC:0135-0235-02160 in 1 BOTTLE; Type 0: Not a Combination Product07/23/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00106/21/2021
    Labeler - Haleon US Holdings LLC (079944263)
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