Label: CALCIUM ANTACID- calcium carbonate tablet, chewable

  • NDC Code(s): 69168-219-02, 69168-219-50
  • Packager: Allegiant Health
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 8, 2017

If you are a consumer or patient please visit this version.

View All Sections
  • Active ingredient (in each tablet)

    Calcium Carbonate 500 mg

  • Purpose

    Antacid 

  • Uses

    relieves

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

    Ask a doctor or pharmacist before use if you

    • have kidney disease
    • are taking a prescription drug. Antacids may interact with certain prescription drugs

    When using this product

    • do not take more than 15 tablets in 24 hours
    • if pregnant, do not take more than 10 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: calcium 200mg
    • store at 15º-30ºC (59º-86ºF) 
    • do not use if imprinted safety seal under cap is broken or missing
  • Inactive ingredients

    assorted flavors, D&C yellow #10 aluminum lake, dextrose, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin

  • Package/Label Principal Display Panel

    SODIUM FREE

    Health A2Z®

    CALCIUM ANTACID
    REGULAR STRENGTH
    500 mg
    Calcium Supplement

    Fast Relief of...

    • Sour & Upset Stomach
    • Acid Indigestion
    • Heartburn 

    *Compare to Tums® Active Ingredient

    Assorted Fruit

    Chewable Tablets

    Antacid

    Antacid

  • INGREDIENTS AND APPEARANCE
    CALCIUM ANTACID 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69168-219
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE500 mg
    Inactive Ingredients
    Ingredient NameStrength
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    Product Characteristics
    Coloryellow, orange, pink, greenScoreno score
    ShapeROUNDSize16mm
    FlavorLIME, CHERRY, ORANGE, LEMONImprint Code AZ;024
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69168-219-5050 in 1 BOTTLE; Type 0: Not a Combination Product12/16/201405/15/2023
    2NDC:69168-219-02150 in 1 BOTTLE; Type 0: Not a Combination Product05/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00112/16/2014
    Labeler - Allegiant Health (079501930)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!