Label: EQUALINE REGULAR STRENGTH ANTACID PEPPERMINT- calcium carbonate tablet, chewable

  • NDC Code(s): 41163-132-17
  • Packager: UNITED NATURAL FOODS, INC. DBA UNFI
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 30, 2024

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

  • ACTIVE INGREDIENT (in each tablet)

    Calcium carbonate 500 mg

  • PURPOSE

    Antacid

  • USES

    relieves:

    • acid indigestion
    • heartburn
  • 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 15 tablets in a 24-hour period, or use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a doctor.

  • IF PREGNANT OR BREAST FEEDING,

    ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    .

  • DIRECTIONS

    • adults and children 12 years of age and over:
    • Wet in mouth before chewing
    • chew 2-4 tablets as symptoms occur, or as directed by a doctor.
  • OTHER INFORMATION

    • each tablet contains: elemental calcium 200 mg
    • do not use if printed seal under the cap is torn or missing.
    • store at room temperature. keep the container tightly closed.
  • INACTIVE INGREDIENTS

    corn starch, crospovidone, dextrose, flavor, magnesium stearate, maltodextrin, sucrose, talc.

  • PRINCIPAL DISPLAY PANEL

    NDC 41163-132-17

    Compare to Tums® Regular Strength 500 active ingredient* 

    EQUALINE®
    regular Strength
    antacid tablets
    Calcium Carbonate 500 mg

     
    relieves:

    heartburn and

    acid Indigestion



    peppermint flavor

    150 chewable tablets

     

      

    equ-113.jpg

  • INGREDIENTS AND APPEARANCE
    EQUALINE REGULAR STRENGTH ANTACID PEPPERMINT 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41163-132
    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
    STARCH, CORN (UNII: O8232NY3SJ)  
    DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    SUCROSE (UNII: C151H8M554)  
    TALC (UNII: 7SEV7J4R1U)  
    CROSPOVIDONE, UNSPECIFIED (UNII: 2S7830E561)  
    Product Characteristics
    ColorWHITEScoreno score
    ShapeROUNDSize16mm
    FlavorPEPPERMINTImprint Code G113
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:41163-132-17150 in 1 BOTTLE; Type 0: Not a Combination Product04/30/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph Drugpart33104/30/2024
    Labeler - UNITED NATURAL FOODS, INC. DBA UNFI (943556183)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guardian Drug Company119210276MANUFACTURE(41163-132)