Label: ANTACID- calcium carbonate tablet

  • NDC Code(s): 11673-481-14, 11673-481-83, 11673-722-01
  • Packager: Target Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

NOTE: Most over the counter (OTC) are not reviewed and approved by the 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 12/14

If you are a consumer or patient please visit this version.

  • Active ingredient (per tablet)

    Calcium Carbonate USP 1,000 mg

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  • Purpose

    Antacid

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  • Uses

    relieves

    heartburn
    acid indigestion
    sour stomach
    upset stomach associated with these symptoms
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  • 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.

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  • 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
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  • Other information

    each tablet contains: elemental calcium 400mg, sodium 2mg (Assorted Fruit)
    store below 30 oC (86 oF)
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  • 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

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  • Inactive ingredients (Peppermint)

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

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  • Questions?

    Call 1-888-367-7919 weekdays

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  • Principal Display Panel

    NDC 11673-481-41

    antacid tablets

    ultra strength

    calcium carbonate

    1000mg

    Compare to Tums Ultra®* 

    up&upTM

    assorted fruit flavor

    160 CHEWABLE TABLETS

    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 0457 ID271409

    Distributed by Target Corporation

    Minneapolis, MN 55403

    ©2014 Target Brands, Inc.

    All Rights Reserved

    Shop Target.com

    Gluten-Free

    103748XA (front label)

    103747XA (back label)

    Antacid Target 160 count front label
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  • 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
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  • INGREDIENTS AND APPEARANCE
    ANTACID 
    calcium carbonate tablet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11673-481
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (CARBONATE ION and CALCIUM CATION) CALCIUM CARBONATE 1000 mg
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE  
    STARCH, CORN  
    TALC  
    MINERAL OIL  
    ADIPIC ACID  
    SODIUM POLYMETAPHOSPHATE  
    FD&C RED NO. 40  
    FD&C YELLOW NO. 6  
    FD&C YELLOW NO. 5  
    FD&C BLUE NO. 1  
    ALUMINUM OXIDE  
    Product Characteristics
    Color PINK (orange, yellow, green) Score no score
    Shape ROUND Size 19mm
    Flavor CHERRY (assorted fruit, orange, lemon, lime) Imprint Code LH20
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-481-83 72 in 1 BOTTLE; Combination Product Type = C112160 02/15/2010
    2 NDC:11673-481-14 160 in 1 BOTTLE; Combination Product Type = C112160 02/15/2010
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part331 02/15/2010
    ANTACID 
    calcium carbonate tablet
    Product Information
    Product Type HUMAN OTC DRUG LABEL Item Code (Source) NDC:11673-722
    Route of Administration ORAL DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    CALCIUM CARBONATE (CARBONATE ION and CALCIUM CATION) CALCIUM CARBONATE 1000 mg
    Inactive Ingredients
    Ingredient Name Strength
    SUCROSE  
    STARCH, CORN  
    TALC  
    MINERAL OIL  
    SODIUM POLYMETAPHOSPHATE  
    Product Characteristics
    Color WHITE Score no score
    Shape ROUND Size 19mm
    Flavor PEPPERMINT Imprint Code LH20
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:11673-722-01 160 in 1 BOTTLE; Combination Product Type = C112160 03/08/2013
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part331 03/08/2013
    Labeler - Target Corporation (006961700)
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