Label: ANTACID- calcium carbonate tablet

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated October 21, 2016

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  • Active ingredient (per tablet)

    Calcium Carbonate USP 1000 mg

  • Purpose

    Antacid

  • Uses

    relieves

    •
    heartburn
    •
    acid indigestion
    •
    sour stomach
    •
    upset stomach associated with these symptoms
  • 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 24 hours
    •
    If pregnant do not take more than 5 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 2-3 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: elemental calcium 400mg, sodium 2mg (Assorted Fruit)
    •
    store below 30oC (86oF)
  • Inactive ingredients (Assorted Fruit)

    adipic acid, corn starch, FD&C blue #1 lake, FD&C red #40 lake, FD&C yellow #5 (tartrazine) lake, FD&C yellow #6 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

  • Inactive ingredients (Peppermint)

    sucrose, calcium carbonate, corn starch, talc, mineral oil, natural flavor, sodium polyphosphate

  • Questions?

    Call 1-888-367-7919 weekdays

  • Principal Display Panel

    NDC 11673-481-41

    ultra strength

    antacid 1000

    calcium carbonate

    Compare to Tums Ultra®* 

    relief of heartburn

    acid indigestion and

    upset stomach

    associated with these symptoms

    up&up®

    ASSORTED FRUIT FLAVOR

    160 CHEWABLE TABLETS

    naturally and artificially flavored

    Safety sealed- Do not use if printed inner seal beneath cap is missing or broken.

    *TUMS and TUMS ULTRA are registered trademarks of the GSK group of companies.

    245 05 0457 R00 ID285492

    Dist. by Target Corp., Mpls., MN 55403

    ©2015 Target Brands, Inc.

    Shop Target.com

    GLUTEN FREE

    103748XB (front label)

    103747XB (back label)

    Antacid Target 160 count front label
  • Principal Display Panel

    NDC 11673-722-01

    antacid tablets

    ultra strength antacid/calcium supplement

    calcium carbonate, 1,000 mg

    Compare to active ingredient in TUMS® Ultra*

    up & up®

    160 CHEWABLE TABLETS

    naturally flavored

    peppermint flavor

    CALCIUM SUPPLEMENT

    USES: As a daily source of extra calcium.

    DIRECTIONS: Chew 2 tablets once or twice daily with a meal.

    Supplement Facts

    Serving Size: 2 Tablets

    Servings Per Container: 80

    Amount Per Serving

    %Daily Value

    Calories 10

    Sugars 3g

    Calcium 800mg

    80%

    Sodium 10mg

    Less than 1%

    Safety sealed- Do not use if printed inner seal beneath cap is missing or broken.

    *TUMS and TUMS ULTRA are registered trademarks of the GlaxoSmithKline group of companies.

    245 05 0049 ID083403

    Dist. by Target Corporation

    Minneapolis, MN 55403

    ©2013 Target Brands, Inc.

    Shop Target.com

    Guest Services 1-800-910-6874

    GLUTEN FREE

    Front Label: 102801XA

    Back Label: 102802XA

    Target Antacid 160 ct peppermint label
  • INGREDIENTS AND APPEARANCE
    ANTACID 
    calcium carbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-481
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    ADIPIC ACID (UNII: 76A0JE0FKJ)  
    SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Product Characteristics
    ColorPINK (orange, yellow, green) Scoreno score
    ShapeROUNDSize19mm
    FlavorCHERRY (assorted fruit, orange, lemon, lime) Imprint Code LH20
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-481-14160 in 1 BOTTLE; Type 0: Not a Combination Product02/15/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33102/15/2010
    ANTACID 
    calcium carbonate tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-722
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    SODIUM POLYMETAPHOSPHATE (UNII: P1BM4ZH95L)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUNDSize19mm
    FlavorPEPPERMINTImprint Code LH20
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-722-01160 in 1 BOTTLE; Type 0: Not a Combination Product03/08/201306/30/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33103/08/201306/30/2018
    Labeler - Target Corporation (006961700)
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