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Prescription Information


  • Active ingredient (per tablet)

    Calcium Carbonate USP 1000 mg

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  • Purpose

    Antacid

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  • Uses

    relieves

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

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  • 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
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  • Other information

    each chewable tablet contains: elemental calcium 400mg
    do not store below 25 oC (77 oF)

     

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  • Inactive ingredients (Tropical Fruit)

    cellulose, dextrose, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6 alum lake, flavor, maltodextrin, mineral oil, polyethylene glycol, talc

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  • Inactive ingredient (Mint)

    cellulose, dextrose, flavor, maltodextrin, mineral oil, polyethylene glycol, talc

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  • Questions?

    1-800-897-7535

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  • Principal Display Panel

    NDC 0135-0610-01

    TUMS®

    CALCIUM CARBONATE

    ANTACID

    GOES TO WORK IN SECONDS!

    TROPICAL FRUIT

    ULTRA STRENGTH 1000

    72 CHEWABLE TABLETS

    ©2014 GSK

    PAREVE

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

    Trademarks are owned by or licensed to the GSK group of companies.

    Dist. by:

    GSK Consumer Healthcare

    Warren, NJ 07059

    ©2014 GSK or its licensor

    105439XA (Front Label)

    105440XA (Back Label)

    Tums Ultra Tropical Fruit 72 count front label
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  • Principal Display Panel

    NDC 0135-0612-01

    TUMS®

    CALCIUM CARBONATE

    ANTACID

    GOES TO WORK IN SECONDS!

    MINT

    ULTRA STRENGTH 1000

    72 CHEWABLE TABLETS

    PAREVE

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

    Trademarks are owned by or licensed to the GSK group of companies.

    Dist. by:

    GSK Consumer Healthcare

    Warren, NJ 07059

    ©2014 GSK or its licensor

    105430XA (Front Label)

    105431XA (Back Label)

    Tums Ultra Mint 72 count front label
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  • INGREDIENTS AND APPEARANCE
    TUMS  ULTRA
    calcium carbonate tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0610
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 1000 mg
    Inactive Ingredients
    Ingredient Name Strength
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Color RED (red, yellow, orange, off white) Score no score
    Shape ROUND Size 19mm
    Flavor TROPICAL FRUIT PUNCH (tropical fruit: tropical punch, banana, tropical orange, pineapple) Imprint Code TUMS
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0135-0610-01 72 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2016
    2 NDC:0135-0610-02 160 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part331 09/01/2016
    TUMS  ULTRA
    calcium carbonate tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0612
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 1000 mg
    Inactive Ingredients
    Ingredient Name Strength
    POWDERED CELLULOSE (UNII: SMD1X3XO9M)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Color WHITE Score no score
    Shape ROUND Size 19mm
    Flavor PEPPERMINT Imprint Code TUMS
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0135-0612-01 72 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2016
    2 NDC:0135-0612-02 160 in 1 BOTTLE; Type 0: Not a Combination Product 09/01/2016
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part331 09/01/2016
    Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)
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