Label: QUALITY CHOICE CHEWABLE ANTACID ASSORTED FRUIT- antacid tablets tablet, chewable

  • NDC Code(s): 63868-047-15
  • Packager: Chain Drug Marketing Association
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 18, 2024

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  • Active ingredient

    Calcium carbonates USP 500mg

  • 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 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

    • do not use the maximum dosage for more than 2 weeks.

  • Keep out of Reach of Children

  • Directions

    • Chew 2-4 tablets as symptoms occur, or as directed by a doctor.

  • Other Information

    • Store below 30°C (86°F).

    • Keep the container tightly closed

    • For calcium and magnesium content see Supplement Facts.

  • Inactive ingredients

    adipic acid, D&C Red No. 27, D&C Yellow No. 10, dextrose, FD&C Blue No. 1, FD&C Yellow No. 6, flavors, magnesium stearate, maltodextrin, starch, sucralose.

    Safety sealed: Do not use if printed seal under cap is torn or missing

  • Package/Label Principal Display Panel

    Compare to Tums Regular Strength active ingredient*

    NDC 63868-047-15

    Quality Choice

    Regular Strength

    Antacid Tablets

    Antacid Calcium Supplement

    Calcium Carbonate 500mg

    Relieves:

    Upset Stomach

    Heartburn

    Acid Indigestion

    Assorted Fruit

    150 Chewable Tablets

    Quality Choice Regular strength Antacid Tablets 150 Count

    Quality Choice Regular Strength Antacid Tablets

    Quality Choice Regular Strength Antacid Tablets

  • INGREDIENTS AND APPEARANCE
    QUALITY CHOICE CHEWABLE ANTACID  ASSORTED FRUIT
    antacid tablets tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-047
    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
    ADIPIC ACID (UNII: 76A0JE0FKJ)  
    D&C RED NO. 27 (UNII: 2LRS185U6K)  
    D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    Product Characteristics
    ColorRED, YELLOW, ORANGEScoreno score
    ShapeROUNDSize16mm
    FlavorFRUITImprint Code RP101
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63868-047-15150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product02/07/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00102/07/2014
    Labeler - Chain Drug Marketing Association (011920774)
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