Label: PHYSICIANSCARE ANTACID- calcium carbonate tablet, chewable

  • NDC Code(s): 0924-0086-00, 0924-0086-01, 0924-0086-02, 0924-0086-03
  • Packager: Acme United 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 March 14, 2023

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  • ACTIVE INGREDIENT

    Drug Facts

    Active Ingredient (in each tablet)

    Calcium Carbonate 420 mg

  • PURPOSE

    Purpose

    Antacid

  • INDICATIONS & USAGE

    Uses

    relieves

    ■ acid indigestion

    ■ sour stomach

    ■ heartburn

    ■ upset stomach associated with these symptoms

  • WARNINGS

    Warnings

  • ASK DOCTOR/PHARMACIST

    Ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs.

  • WHEN USING

    When using this product

    • do not take more than 19 tablets in 24 hours
    • do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a physician
    • do not exceed recommended dosage
  • STOP USE

    Stop using this product and ask a doctor if

    • symptoms last more than 2 weeks
  • PREGNANCY OR BREAST FEEDING

    If you are pregnant or breastfeeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    • do not use more than directed

    Adults and children (12 years and older) Chew 2 tablets every 2 or 3 hours as symptoms occur or as directed by a physician. Do not take more than 19 tablets in 24 hours.

    Children under 12 years:

    Do not give to children under 12 years of age

  • INFORMATION FOR PATIENTS

    Other information

    • each tablet contains 168 mg of elemental calcium
    • phenylketonurics: contains phenylalanine 1.5 mg per tablet
    • store at room temperature 59-86F (15-30C) in a dry place
    • tamper-evident sealed packets
    • do not use any opened or torn packets
  • INACTIVE INGREDIENT

    Inactive ingredients

    aspartame, croscarmellose sodium, magnesium stearate, maltodextrin, mint flavor, sorbitol

  • QUESTIONS

    Questions?1-800-835-2263

  • Physicians Care Antacid Label

    90089

    Physicians Care®

    Antacid

    Calcium Carbonate

    Pull To Open

    Chewable Tablets

    Tamper-Evident Packets of 2 Tablets

    Do not use if packet is open or torn.

    Calcium Carbonate 420 mg

    100 Tablest (50 Packets, 2 each)

    101R 90089

  • INGREDIENTS AND APPEARANCE
    PHYSICIANSCARE ANTACID 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0924-0086
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE420 mg
    Inactive Ingredients
    Ingredient NameStrength
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    ASPARTAME (UNII: Z0H242BBR1)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    Colorwhite (white) Scoreno score
    ShapeROUND (ROUND) Size11mm
    FlavorMINT (MINT) Imprint Code AZ;036
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0924-0086-0150 in 1 CARTON11/28/2011
    12 in 1 PACKET; Type 0: Not a Combination Product
    2NDC:0924-0086-02125 in 1 CARTON11/28/2011
    22 in 1 PACKET; Type 0: Not a Combination Product
    3NDC:0924-0086-0310 in 1 CARTON11/28/2011
    32 in 1 PACKET; Type 0: Not a Combination Product
    4NDC:0924-0086-002 in 1 PACKET; Type 0: Not a Combination Product11/28/2011
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart33111/28/2011
    Labeler - Acme United Corporation (001180207)
    Registrant - Prestige Packaging (170837962)
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