ULTRA STRENGTH ANTACID (CALCIUM ANTACID) TABLET, CHEWABLE [CVS]

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  • ULTRA STRENGTH ANTACID (CALCIUM ANTACID) TABLET, CHEWABLE [CVS]

ULTRA STRENGTH ANTACID (CALCIUM ANTACID) TABLET, CHEWABLE [CVS]
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NDC 69842-171-68, 69842-171-72
Set ID 51acc196-ab1f-49ea-8a59-f06309f1953b
Category HUMAN OTC DRUG LABEL
Packager CVS
Generic Name
Product Class
Product Number
Application Number PART331
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  • Active ingredient (in each tablet)

    Calcium carbonate 1000 mg

  • Purpose

    Antacid

  • KEEP OUT OF REACH OF CHILDREN


  • Uses

    relieves

    • acid indigestion
    • heartburn
  • 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 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 2-3 tablets as symptoms occur, or as directed by a doctor.

    Other information

    • each tablet contains: elemental calcium 400 mg
    • do not use if printed seal under cap is torn or missing.
    • store at room temperature. keep the container tightly closed.
  • Inactive ingredients

    adipic acid, corn starch, crospovidone, D&C red 27 lake, D&C red 30 lake, D&C yellow 10 lake, dextrose, FD&C blue 1 lake, FD&C yellow 6 lake, flavors, magnesium stearate, maltodextrin, sucrose, talc.

  • Principal Display Panel

    CVS Health

    Compare to active ingredient in TUMS® Ultra strength 

    Ultra Strength Antacid Tablets

    Calcium Carbonate 1000 mg

    Assorted Fruit Flavor

    72 Chewable Tablets

    Label

  • INGREDIENTS AND APPEARANCE
    ULTRA STRENGTH ANTACID 
    calcium antacid tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-171
    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)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    CROSPOVIDONE (UNII: 2S7830E561)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    D&C RED NO. 30 (UNII: 2S42T2808B)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    Product Characteristics
    Colororange, yellow, green, pink (reddish-pink) Scoreno score
    ShapeROUNDSize17mm
    FlavorFRUIT (orange, cherry, lemon, lime) Imprint Code G171
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69842-171-6872 in 1 BOTTLE; Type 0: Not a Combination Product12/09/2011
    2NDC:69842-171-72160 in 1 BOTTLE; Type 0: Not a Combination Product12/09/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33112/09/2011
    Labeler - CVS (062312574)
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