Label: MEDIQUE BAN-ACID MAXIMUM STRENGTH 750- calcium carbonate tablet, chewable

  • NDC Code(s): 47682-285-33, 47682-285-36, 47682-285-99
  • Packager: Unifirst First Aid Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph final

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 July 12, 2022

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredient (in each tablet)

    Calcium Carbonate USP 750 mg

  • PURPOSE

    Purpose

    Antacid

  • INDICATIONS & USAGE

    Uses

    relieves

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

    Warnings

  • DO NOT USE

    Do not use

    ■ the maximum dosage of this product for more than 2 weeks except under the advice and

    supervision of a doctor

  • ASK DOCTOR

    Ask a doctor or pharmacist before use if you

    • are taking a prescription drug. Antacids may interact with certain prescription drugs.
    • have kidney disease
  • WHEN USING

    When using this product

    • do not take more than 10 tablets in a 24 hours
    • if pregnant, do not take more than 6 tablets in 24 hours
  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    ■ do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

    Adults and children: (12 years and over): Chew 2 to 4 tablets as symptoms occur, or as directed by a doctor.

    Children under 12 years: Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    • calcium content per tablet: 300 mg
    • 5 calories per tablet
    • store at room temperature 59-86ºF (15-30ºC)
    • tamper-evident sealed packets
    • do not use any opened or torn packets
  • INACTIVE INGREDIENT

    Inactive ingredients

    assorted flavors, dextrose, FD&C blue #1 aluminum lake, FD&C red #40 aluminum lake, magnesium stearate, maltodextrin, mineral oil

  • QUESTIONS

    Questions or comments? Call 1-800-634-7680

  • Medique Ban-acid Label

    Medique®

    Ban-acid

    Maximum Strength 750

    Calcium Rich Extra Strength Antacid

    Antiacido extra fuerte y /ricas en calcio

    Pull To Open

    Tire Para Abrir

    √ Heartburn, Indigestion,•Calcium Carbonate 750mg

    las agruras, la indigestion•Carbonato de Caldo 750mg

    Assorted Berry

    Bayas surtidas

    100

    Tablets

    (50 x 2)

    Tamper Evident Unit Dose Packets

    Empaquetado con Sellado Evidente en Dosis Unitarias

    285R Banacid

  • INGREDIENTS AND APPEARANCE
    MEDIQUE BAN-ACID  MAXIMUM STRENGTH 750
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:47682-285
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
    Inactive Ingredients
    Ingredient NameStrength
    MINERAL OIL (UNII: T5L8T28FGP)  
    DEXTROSE (UNII: IY9XDZ35W2)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    Product Characteristics
    Colorred (RED) , purple (PURPLE) , gray (GRAY) Scoreno score
    ShapeROUND (ROUND) Size15mm
    FlavorSTRAWBERRY (Blueberry Blackberry) Imprint Code RH;031
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:47682-285-3350 in 1 BOX09/29/2017
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:47682-285-992 in 1 PACKET; Type 0: Not a Combination Product07/01/2014
    3NDC:47682-285-3675 in 1 BOX04/01/2019
    32 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33107/01/2014
    Labeler - Unifirst First Aid Corporation (832947092)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!