Label: D-CAL- calcium carbonate tablet, chewable

  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated October 3, 2019

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  • Active ingredient (in each tablet)

    Calcium Carbonate 750 mg

    Purpose

    Antacid

    Uses

    relieves

    • heartburn
    • acid indigestion
    • sour stomach
    • upset stomach due to these symptoms

    Warnings

    Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product

    • do not take more than 10 tablets for adults and 5 tablets for children in a 24 hour period.

    Keep out of reach of children.

    Directions

    • Adults: chew 2 tablets daily.
    • Children: chew 1 tablet daily. If symptoms persist, ask a doctor.

    Other information

    • Store in a dry place
    • do not use if imprinted seal under cap is torn or open

    Inactive ingredients

    Cholecalciferol, D&C red #27, flavors, magnesium stearate, sorbitol

  • PRINCIPAL DISPLAY PANEL

    D-Cal_60 Chewable Tab_Hauppauge.jpg

  • INGREDIENTS AND APPEARANCE
    D-CAL 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62211-166
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
    Inactive Ingredients
    Ingredient NameStrength
    CHOLECALCIFEROL (UNII: 1C6V77QF41)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorpinkScoreno score
    ShapeRECTANGLESize17mm
    FlavorTROPICAL FRUIT PUNCHImprint Code DCAL;AZ
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62211-166-6060 in 1 BOTTLE; Type 0: Not a Combination Product09/17/1997
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33109/17/1997
    Labeler - A&Z Pharmaceutical Inc. (080225262)
    Registrant - A&Z Pharmaceutical Inc. (080225262)
    Establishment
    NameAddressID/FEIBusiness Operations
    A&Z Pharmaceutical Inc.080225262manufacture(62211-166)
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