Label: ANTACID RELIEF- calcium carbonate tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 12, 2022

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  • Active ingredient (in each tablet)

    Calcium carbonate 500 mg

  • Purpose

    Antacid

  • KEEP OUT OF REACH OF CHILDREN

  • Uses

    relieves

    • acid indigestion
    • heartburn
  • WARNINGS

    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 15 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

    If pregnant or breast-feeding, ask a health professional before use.

    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.
  • Other information

    • each tablet contains: elemental calcium 200 mg
    • do not use if printed seal under the cap is torn or missing.
    • store at room temperature. keep the container tightly closed.
  • Inactive ingredients

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

  • Principal Display Panel

    COMPARE TO TUMS® active ingredient* 

    Signature Care

    Regular Strength Anatcid Relief Tablets

    CALCIUM CARBONATE 500 mg

    PEPPERMINT FLAVOR

    • Chewable
    • Rich in calcium
    • Relief of: acid indigestion/heartburn

    150 Tablets

    image description

  • INGREDIENTS AND APPEARANCE
    ANTACID RELIEF 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:21130-913
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE500 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSPOVIDONE (UNII: 2S7830E561)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize16mm
    FlavorPEPPERMINTImprint Code GDC113
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:21130-913-17150 in 1 BOTTLE; Type 0: Not a Combination Product08/08/2015
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33108/08/2015
    Labeler - Safeway (009137209)
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