Label: ANTACID- CALCIUM CARBONATE- calcium carbonate tablet, chewable

  • NDC Code(s): 87745-001-01
  • Packager: Anhui Jiuhe Health Industry Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 2, 2026

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  • Active Ingredient

    Calcium carbonate 1000 mg

  • Purpose

    Antacid

  • Use

    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.

  • Do not use

    Do not take more than 8 tablets in 24 hours. Do not use the maximum dosage for more than 2 weeks except under advice and supervision of a doctor. If pregnant, do not take more than 4 tablets in 24 hours.

  • When Using

    Do not swallow tablets whole. Keep the container tightly closed.

  • Stop Use

    Do not take for symptoms that persist for more than 2 weeks unless advised by a doctor.

  • Ask Doctor

    If pregnant or breast-feeding, ask a health professional before use.

  • Keep Out Of Reach Of Children

    Keep out of reach of children.

  • Directions

    Adults and children 12 years of age and over: chew 2–4 tablets completely as symptoms occur, 2 times daily or as directed by a doctor.

  • Other information

    Each tablet contains calcium 400 mg. Store at room temperature 68–77°F (20–25°C). Contains FD&C Yellow No.5 (tartrazine) as color additive.

  • Inactive ingredients

    Corn starch, FD&C Blue No.1 aluminum lake, FD&C Yellow No.5 aluminum lake, flavors, magnesium stearate, maltitol, sucralose, sucrose

  • Questions

    Questions? Call 1-800-255-0711

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    ANTACID- CALCIUM CARBONATE 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:87745-001
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE1000 mg
    Inactive Ingredients
    Ingredient NameStrength
    STARCH, CORN (UNII: O8232NY3SJ)  
    FD&C BLUE NO. 1 ALUMINUM LAKE (UNII: J9EQA3S2JM)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTITOL (UNII: D65DG142WK)  
    SUCRALOSE (UNII: 96K6UQ3ZD4)  
    SUCROSE (UNII: C151H8M554)  
    FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7)  
    Product Characteristics
    ColorgreenScorescore with uneven pieces
    ShapeROUNDSize90mm
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:87745-001-0112 in 1 BOTTLE; Type 0: Not a Combination Product06/03/2026
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00106/03/2026
    Labeler - Anhui Jiuhe Health Industry Co., Ltd (444169621)
    Establishment
    NameAddressID/FEIBusiness Operations
    Anhui Jiuhe Health Industry Co., Ltd444169621manufacture(87745-001)