Label: GAS-X TOTAL RELIEF MAXIMUM STRENGTH- calcium carbonate, simethicone tablet, chewable

  • NDC Code(s): 0067-0118-02, 0067-0118-03
  • Packager: Haleon US Holdings LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 5, 2024

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  • Active ingredients (per tablet)

    Calcium carbonate 750 mg

    Simethicone 250 mg

  • Purpose

    Antacid

    Antigas

  • Uses

    for the relief of

    • pressure, bloating, and fullness commonly referred to as gas
    • gas associated with heartburn, sour stomach, or acid indigestion
    • acid indigestion
    • heartburn
    • sour stomach
    • upset stomach associated with these symptoms
  • Warnings

    Ask a doctor or pharmacist before use if you are

    presently taking a prescription drug. Antacids may interact with certain prescription drugs.

    When using this product

    • do not exceed 2 tablets in 24 hours except under the advice and supervision of a doctor
    • do not use the maximum dosage for more than 2 weeks, except under the advice and supervision of a doctor

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

    Keep out of reach of children.

  • Directions

    • adults and children 12 years and older:chew 1 or 2 tablets as symptoms occur, or as directed by a doctor. Chew or crush tablets completely before swallowing.
    • do not take for symptoms that persist for more than 2 weeks, unless advised by a doctor
  • Other information

    • each tablet contains:elemental calcium 295 mg
    • store in a cool, dry place at no higher than 25°C (77°F)
    • contains FD&C Yellow 5 Lake (tartrazine) as a color additive
  • Inactive ingredients

    alcohol, ammonium hydroxide, beeswax, carnauba wax, citric acid, corn syrup, dextrin, ethyl acetate, FD&C red 40, FD&C red 40 lake, FD&C yellow 5 lake (tartrazine), FD&C yellow 6, FD&C yellow 6 lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methylparaben, n-butyl alcohol, pharmaceutical ink, phosphoric acid, propylene glycol, propylparaben, purified water, shellac,

    sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, vegetable oil (coconut origin)

  • Questions or comments?

    1-855-328-5204

  • Additional Information

    TAMPER EVIDENT FEATURE:Do not use if printed inner safety seal under cap is broken or missing.

    Dist. by: GSK CH,Warren, NJ 07059

    Trademarks owned or licensed by GSK.

    ©2021 GSK or licensor.

    1001392

  • Principal Display Panel

    NEW#1 DOCTOR RECOMMENDED BRAND

    NDC 0067-0118-03

    Gas-X

    TOTAL RELIEF*

    Simethicone / Antigas

    Calcium Carbonate / Antacid

    *Provides gas and heartburn relief

    Fast Relief

    √ GAS √ HEARTBURN √ BLOATING √ DISCOMFORT

    MAXIMUM

    STRENGTH

    250 mg Simethicone

    Mixed Berries

    30 Chewable Tablets

    1001392 – Front Carton

    1001392_Gas X Total Relief_30 chewable tabs
  • INGREDIENTS AND APPEARANCE
    GAS-X   TOTAL RELIEF MAXIMUM STRENGTH
    calcium carbonate, simethicone tablet, chewable
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0067-0118
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE750 mg
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE250 mg
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    AMMONIA (UNII: 5138Q19F1X)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    CORN SYRUP (UNII: 9G5L16BK6N)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    ETHYL ACETATE (UNII: 76845O8NMZ)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    ACACIA (UNII: 5C5403N26O)  
    ISOPROPYL ALCOHOL (UNII: ND2M416302)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    BUTYL ALCOHOL (UNII: 8PJ61P6TS3)  
    PHOSPHORIC ACID (UNII: E4GA8884NN)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    WATER (UNII: 059QF0KO0R)  
    SHELLAC (UNII: 46N107B71O)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    SORBIC ACID (UNII: X045WJ989B)  
    SORBITOL (UNII: 506T60A25R)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    SUCROSE (UNII: C151H8M554)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    CORN OIL (UNII: 8470G57WFM)  
    Product Characteristics
    Colorpurple (Red) Scoreno score
    ShapeROUNDSize19mm
    FlavorBERRY (Mixed Berries, Strawberry) Imprint Code GT
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0067-0118-031 in 1 CARTON02/03/2022
    130 in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:0067-0118-021 in 1 CARTON02/03/2022
    265 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00102/03/2022
    Labeler - Haleon US Holdings LLC (079944263)
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