Label: ANTACID EXTRA STRENGTH- calcium carbonate tablet, chewable

  • NDC Code(s): 11673-479-03, 11673-480-03, 11673-726-01, 11673-726-02, view more
    11673-726-03
  • Packager: Target Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 21, 2024

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

  • Active ingredient (per tablet)

    Calcium Carbonate USP 750 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 10 tablets in 24 hours
    • if pregnant do not take more than 6 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 – 4 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 300mg, sodium 2mg
    • store below 30 oC (86 oF)
  • Inactive ingredients (Assorted Berry)

    adipic acid, corn starch, FD&C blue #1 lake, FD&C red #40 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

  • Inactive ingredients (Assorted Tropical Fruit)

    corn startch, FD&C red #40 lake, FD&C yellow #5(tartrazine) lake, FD&C yellow #6 lake, flavors, mineral oil, sodium polyphosphate, sucrose, talc

  • Questions?

    1-888-367-7919 weekdays

  • Principal Display Panel

    NDC 11673-479-03

    extra strength

    antacid 750

    calcium carbonate

    Compare to Tums ®Extra Strength*

    relief of heartburn

    acid indigestion and

    upset stomach

    associated with

    these symptoms

    up&up ®

    ASSORTED BERRY FLAVOR

    96 CHEWABLE TABLETS

    artificially flavored

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

    *TUMS ®is a registered trademark of the GSK group of companies.

    245 05 0459 R00 ID285492

    Distributed by Target Corporation

    Minneapolis, MN 55403

    ©2015 Target Brands, Inc.

    Shop Target.com

    GLUTEN FREE

    103741XB (front label)

    103740XB (back label)

    antacid extra strength berry Target 96 count front label
  • Principal Display Panel

    NDC 11673-480-03

    extra strength

    antacid 750

    calcium carbonate

    Compare to Tums ®Extra Strength*

    relief of heartburn

    acid indigestion and

    upset stomach

    associated with

    these symptoms

    up&up ®

    TROPICAL FRUIT FLAVOR

    96 CHEWABLE TABLETS

    Naturally and artificially flavored

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

    *TUMS ®is a registered trademark of the GSK group of companies.

    245 05 0458 R00 ID285492

    Distributed by Target Corporation

    Minneapolis, MN 55403

    ©2015 Target Brands, Inc.

    Shop Target.com

    GLUTEN FREE

    103745XB (front label)

    103744XB (back label)

    antacid extra strength tropical Target 96 count front label
  • Principal Display Panel

    NDC 11673-726-02

    antacid tablets

    extra strength

    calcium carbonate 750mg

    Compare to Tums EX ®*

    Assorted berry flavor

    24 count

    24 CHEWABLE TABLETS

    Retain outer wrap for full drug facts.

    GLUTEN FREE

    245 05 0872 R00 ID074434

    Dist. By Target Corp.

    Minneapolis, MN 55403

    ©2014 Target Brands, Inc.

    Shop Target.com

    Safety sealed-Do not use if plastic overwrap is damaged.

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

    245-05-0872

    103809XB

    antacid extra strength berry Target 24 ct label
  • INGREDIENTS AND APPEARANCE
    ANTACID   EXTRA STRENGTH
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-479
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 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 BLUE NO. 1 (UNII: H3R47K3TBD)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Product Characteristics
    Colorpink (mauve, bluish) Scoreno score
    ShapeROUNDSize16mm
    FlavorSTRAWBERRY (Assorted Berry, raspberry, mixed berry) Imprint Code 3205
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-479-0396 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 DrugM00102/15/2010
    ANTACID   EXTRA STRENGTH
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-480
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
    Inactive Ingredients
    Ingredient NameStrength
    SUCROSE (UNII: C151H8M554)  
    STARCH, CORN (UNII: O8232NY3SJ)  
    TALC (UNII: 7SEV7J4R1U)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    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)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Product Characteristics
    Colorred (red-orange, orange, off-white, light yellow) Scoreno score
    ShapeROUNDSize16mm
    FlavorTROPICAL FRUIT PUNCH (Assorted tropical fruit flavor, tropical punch, mandarin orange, orange-pineapple, strawberry-banana) Imprint Code 3205
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-480-0396 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 DrugM00102/15/2010
    ANTACID   EXTRA STRENGTH
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-726
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 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 BLUE NO. 1 (UNII: H3R47K3TBD)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Product Characteristics
    Colorpink (mauve, bluish) Scoreno score
    ShapeROUNDSize16mm
    FlavorSTRAWBERRY (Assorted Berry, raspberry, mixed berry) Imprint Code 3205
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11673-726-023 in 1 CELLO PACK03/10/2014
    1NDC:11673-726-018 in 1 PACKAGE; Type 0: Not a Combination Product
    2NDC:11673-726-03200 in 1 BOTTLE; Type 0: Not a Combination Product03/10/2014
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00103/10/2014
    Labeler - Target Corporation (006961700)