Label: PHYSICIANSCARE ANTACID- calcium carbonate tablet, chewable

  • NDC Code(s): 0924-0086-00, 0924-0086-01, 0924-0086-02, 0924-0086-03, view more
    0924-0086-04, 0924-0086-05
  • Packager: Acme United Corporation
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 3, 2024

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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
    5NDC:0924-0086-046 in 1 CARTON11/28/2011
    5NDC:0924-0086-002 in 1 PACKET; Type 0: Not a Combination Product
    6NDC:0924-0086-0520 in 1 CARTON11/28/2011
    6NDC:0924-0086-002 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00111/28/2011
    Labeler - Acme United Corporation (001180207)
    Registrant - Prestige Packaging (170837962)
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