Label: TC MAX- calcium carbonate powder, for solution

  • NDC Code(s): 80733-006-01
  • Packager: Romavision Investing LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 3, 2023

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  • Active Ingredients (per 10 grams)

    Calcium Carbonate (588 mg)

  • Purpose

    Antacid

  • Indications

    For the relief of:

    • Heartburn
    • Acid Indigestion
    • Sour Stomach
    • Upset stomach associated with these symptoms
  • Warnings

    • Do not take more than 4 oz within a 24 hour period

    • Do not use the maximum dosage of this product for more than 2 weeks, except under the advice and supervision of a physician

    • If pregnant or breast feeding check with your physician before using

    Ask a doctor before use if you have

    • kidney disease
    • a magnesium restricted diet
    • a calcium restricted diet

    Keep this and all drugs out of the reach of children

  • Drug Interactions

    Ask a doctor or pharmacist before use

    • If you are presently taking a prescription drug antacids may interact with certain prescriptions drugs.
  • Directions for use

    Prepare unit dosage as directed by a physician.

    OTC application is 68 grams per 8oz of water.

  • Other information

    Each canister contains Calcium 15%, Magnesium .85%, Sodium 2.4%

  • Inactive Ingredients:

    Acacia Senegal Whole, Acesulfame-Postasium, Advantame, Artificial Flavor, Glycerin, Magnesium Hydroxide, Neotame, Sodium Bicarbonate, Sucrose, Sunflower Oil Mono and Diglycerides, Tapioca Starch, Thaumatin, Tocopherol Acetate, Tricalcium phosphate, Xanthan Gum

  • Principal Display Panel - 500 gram Canister Label

    Vanilla Ice Cream
    Flavor

    TC MAX

    Buffered Suspension

    500 grams /17.6oz

    Corn Free Soy Free Protein Free Dairy Free Non GMO

    Principal Display Panel - 500 gram Canister Label
  • INGREDIENTS AND APPEARANCE
    TC MAX 
    calcium carbonate powder, for solution
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:80733-006
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    calcium carbonate (UNII: H0G9379FGK) (calcium cation - UNII:2M83C4R6ZB) calcium carbonate4 g  in 237 mL
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    STARCH, TAPIOCA (UNII: 24SC3U704I)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    TRICALCIUM PHOSPHATE (UNII: K4C08XP666)  
    SUNFLOWER OIL MONO/DIGLYCERIDES (UNII: HS7EB0C1ZH)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    NEOTAME (UNII: VJ597D52EX)  
    SODIUM BICARBONATE (UNII: 8MDF5V39QO)  
    MAGNESIUM HYDROXIDE (UNII: NBZ3QY004S)  
    ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)  
    THAUMATIN (UNII: KNC9Q0EE6G)  
    SUCROSE (UNII: C151H8M554)  
    ADVANTAME (UNII: 3ZA6810AWX)  
    ACACIA SENEGAL WHOLE (UNII: QP4QYZ033C)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:80733-006-011740 mL in 1 CANISTER; Type 0: Not a Combination Product07/18/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00106/03/2019
    Labeler - Romavision Investing LLC (080808687)
    Establishment
    NameAddressID/FEIBusiness Operations
    Identipak, Inc.942862350MANUFACTURE(80733-006)
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