Label: ANTACID CALCIUM CARBONATE- calcium carbonate tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 8, 2023

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  • Drug Facts

  • Active Ingredient (in each tablet)

    Calcium Carbonate USP 1000 mg

  • Purpose

    Antacid

  • Uses

    relieves

    • heartburn

    • acid indigestion

    • sour stomach

    • upsetstomach 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

    Keep out of reach of children.

  • Directions

    adults and children 12 years of age and over: chew 2 tablets to 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 400 mg
    • store between 20-25° C (68-77° F)

  • Inactive ingredients

    adipic acid, FD&C Blue No.1 , FD&C RED NO. 40, flavors, magnesium stearate, maltodextrin, microcrystalline cellulose, sugar

  • Principal Display Panel

    NDC 82501-1586-7

    good now TM

    MIXED BERRY

    NATURALLY & ARTIFICIALLY FLAVORED

    Antacid
    Calcium
    Carbonate
    Ultra Strength
    Tablets, 1,000 mg

    Calcium Label

  • INGREDIENTS AND APPEARANCE
    ANTACID CALCIUM CARBONATE 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82501-1586
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CATION1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    ADIPIC ACID (UNII: 76A0JE0FKJ)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)  
    SUCROSE (UNII: C151H8M554)  
    Product Characteristics
    Colorpink (Mauva, Violet) Scoreno score
    ShapeROUNDSize19mm
    FlavorSTRAWBERRY (Raspberry, Mixed Berry) Imprint Code F16
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82501-1586-772 in 1 BOTTLE; Type 0: Not a Combination Product11/07/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00111/07/2023
    Labeler - Gobrands, Inc (057499049)
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