Label: ULINE ANTACID- calcium carbonate tablet, chewable

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 26, 2024

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 420 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/PHARMACIST

    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 19 tablets in a 24 hour period. If symptoms persist for more than 2 weeks. stop using this product and see a doctor.
  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of the reach of children.

  • DOSAGE & ADMINISTRATION

    Directions

    Adults and children: (12 years and older) Chew 2 tablets every 2 - 3 hours as symptoms occur, repeat hourly if needed. Do not exceed 19 tablets in 24 hours.

    Children under 12 years: Ask a doctor

  • OTHER SAFETY INFORMATION

    Other information

    • calcium content per tablet: 168 mg
    • phenylketonurics: each tablet may contain 1.5 mg phenylalanine
    • store at room temperature 59-86°F (15-30°C) 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 or comments? 1-800-295-5510

  • PRINCIPAL DISPLAY PANEL

    ULINE

    ANTACID

    Tamper evident sealed packets:

    Do not use if packet is open or torn.

    Pull to Open

    Calcium Carbonate 420 mg

    • Do not swallow tablets whole

    50 Packets

    2 Tablets Each

    Uline Antacid rev 4-13-21 Label

  • PRINCIPAL DISPLAY PANEL

    ULINE

    ANTACID

    Tamper evident sealed packets:

    Do not use if packet is open or torn.

    ANTACID

    Pull to Open

    Calcium Carbonate 420 mg

    • Do not swallow tablets whole

    50 Packets

    2 Tablets Each

    101R S-18596BX 3-2-23

  • INGREDIENTS AND APPEARANCE
    ULINE ANTACID 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-089
    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)  
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    SUCROSE (UNII: C151H8M554)  
    ACACIA (UNII: 5C5403N26O)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize12mm
    FlavorMINTImprint Code FR;8
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69790-089-3350 in 1 BOX10/07/201903/01/2021
    12 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00110/07/201903/01/2021
    ULINE ANTACID 
    calcium carbonate tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69790-820
    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
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    SORBITOL (UNII: 506T60A25R)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize11mm
    FlavorImprint Code AZ;036
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69790-820-3350 in 1 BOX10/07/2019
    12 in 1 PACKET; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00110/07/2019
    Labeler - Uline (039612668)
    Registrant - Unifirst First Aid Corporation (832947092)
    Establishment
    NameAddressID/FEIBusiness Operations
    Prestige Packaging080667761pack(69790-089, 69790-820)
    Establishment
    NameAddressID/FEIBusiness Operations
    Medique Products086911794pack(69790-820, 69790-089)
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!