Label: TUMS- calcium carbonate tablet

  • NDC Code(s): 0135-1000-01, 0135-1000-02, 0135-1001-01, 0135-1001-02, view more
    0135-1001-03
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 3, 2024

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  • Active ingredient (in each tablet)

    Calcium carbonate 750 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 10 tablets in 24 hours
    • if pregnant do not take more than 6 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 2-4 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 300 mg, magnesium 10 mg
    • store below 30 oC (86 oF)
  • Inactive ingredients (Assorted Berries)

    adipic acid, corn starch, crospovidone, dextrose, FD&C blue 1 lake, FD&C red 40 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc

  • Inactive ingredient (Assorted Fruit)

    adipic acid, corn starch, crospovidone, D&C red 27 lake, D&C red 30 lake, D&C yellow 10 lake, dextrose, FD&C blue 1 lake, FD&C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc

  • Questions?

    1-800-897-7535

  • Additional Information

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

    Dist. by:

    GSK Consumer Healthcare

    Warren, NJ 07059

    ©2021 GSK or licensor.

  • PRINCIPAL DISPLAY PANEL

    NDC 0135-1000-01

    TUMS

    CALCIUM CARBONATE

    ANTACID

    Assorted Berries

    GOES TO WORK IN SECONDS!

    70 CHEWABLE TABLETS

    EXTRA STRENGTH 750

    Front Label: 1001343

    Back Label: 1001344

    Tums Chewable Assorted Berries 70 count label
  • Principal Display Panel

    NDC 0135-1001-01

    TUMS

    CALCIUM CARBONATE

    ANTACID

    Assorted Fruit

    GOES TO WORK IN SECONDS!

    70 CHEWABLE TABLETS

    EXTRA STRENGTH 750

    Front Label: 1001345

    Back Label: 1001346

    Tums Chewable Assorted Fruit 70 count label
  • INGREDIENTS AND APPEARANCE
    TUMS 
    calcium carbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-1000
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE750 mg
    Inactive Ingredients
    Ingredient NameStrength
    ADIPIC ACID (UNII: 76A0JE0FKJ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Colorpink (Red(mauve), Blue(bluish)) Scoreno score
    ShapeROUNDSize16mm
    FlavorBERRY (assorted berries (strawberry, raspberry, wild berry) Imprint Code TUMS
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-1000-0170 in 1 BOTTLE; Type 0: Not a Combination Product10/08/2021
    2NDC:0135-1000-0296 in 1 BOTTLE; Type 0: Not a Combination Product10/08/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00110/08/2021
    TUMS 
    calcium carbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0135-1001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE750 mg
    Inactive Ingredients
    Ingredient NameStrength
    ADIPIC ACID (UNII: 76A0JE0FKJ)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    D&C RED NO. 27 ALUMINUM LAKE (UNII: ZK64F7XSTX)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    D&C YELLOW NO. 10 ALUMINUM LAKE (UNII: CQ3XH3DET6)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Colorpink (Orange, Yellow, Green) Scoreno score
    ShapeROUNDSize16mm
    FlavorFRUIT (assorted fruit (cherry, orange, lemon, lime) Imprint Code TUMS
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0135-1001-0170 in 1 BOTTLE; Type 0: Not a Combination Product10/08/2021
    2NDC:0135-1001-0296 in 1 BOTTLE; Type 0: Not a Combination Product10/08/2021
    3NDC:0135-1001-03330 in 1 BOTTLE; Type 0: Not a Combination Product01/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00110/08/2021
    Labeler - Haleon US Holdings LLC (079944263)
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