Label: CALCIUM CARBONATE tablet, chewable

  • NDC Code(s): 55154-6751-0
  • Packager: Cardinal Health 107, LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 27, 2026

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredient (In Each Tablet)

    Calcium Carbonate USP 500mg

  • Purpose

    Antacid

  • Use

    temporarily relieves:

    •
    Heartburn
    •
    Sour Stomach
    •
    Acid Indigestion
    •
    Upset Stomach Associated With These Symptoms
  • Warnings

    Ask a doctor before use if you have

    •
    kidney disease
    •
    taking any prescription drugs; 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.

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

    Keep out of reach of children.

  • Directions

    Chew 2-4 tablets as symptoms occur, repeat hourly if needed

  • Other Information

    •
    do not use if packet is opened or torn
    •
    Store at controlled room temperature 15° to 30° C (59° to 86° F)
    •
    Calcium content per tablet: 200mg
  • Inactive Ingredients

    FD&C yellow #6 aluminum lake, magnesium stearate, maltodextrin, orange flavor, sorbitol

  • Questions?

    1-866-651-3660 Monday-Friday 8:00am-5:00pm EST

  • .

    Overbagged with 10 chewable tablets per bag, NDC 55154-6751-0

    WARNING: This Unit Dose package is not child resistant and is Intended for Institutional Use Only. Keep this and all drugs out of the reach of children.

    Mfg. by: Allegiant Health, Deer Park, NY 11729

    Dist. By: Hospak® Unit Dose Products, Huntley, IL

    60142

    Hospak®

    Distributed By:

    Cardinal Health

    Dublin, OH 43017

    L33753910124

  • Principal Display Panel

    NDC 55154-6751-0

    CALCIUM CARBONATE 500mg

    (Calcium, Elemental 200mg)

    CHEWABLE ANTACID TABLETS

    10 TABLETS

    500mg bag label
  • INGREDIENTS AND APPEARANCE
    CALCIUM CARBONATE 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55154-6751
    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 YELLOW NO. 6 ALUMINUM LAKE (UNII: GYP6Z2JR6Q)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeROUNDSize15mm
    FlavorCITRUSImprint Code RH;024
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:55154-6751-010 in 1 BAG03/07/201810/31/2026
    11 in 1 BLISTER PACK; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00103/07/201810/31/2026
    Labeler - Cardinal Health 107, LLC (118546603)
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