Label: GAS-X TOTAL RELIEF MAXIMUM STRENGTH- calcium carbonate, simethicone tablet, chewable
- NDC Code(s): 0067-0118-01, 0067-0118-02, 0067-0118-03
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 15, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active ingredients (per tablet)
- Purposes
- Uses
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Warnings
Ask a doctor or pharmacist before use if you are
presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other information
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Inactive ingredients
acacia, beeswax, carmine, carnauba wax, citric acid, corn starch, corn syrup, dextrin, FD&C blue no.2 aluminum, FD&C red no. 40, FD&C red no. 40 aluminum lake, FD&C yellow no. 5 aluminum lake (tartrazine), maltodextrin, medium chain triglycerides, methylparaben, natural and artificial flavors, pharmaceutical ink, phosphoric acid, propylene glycol, propylparaben, purified water, shellac,
sodium benzoate, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, vegetable oil - Questions or comments?
- Additional Information
- Principal Display Panel
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INGREDIENTS AND APPEARANCE
GAS-X TOTAL RELIEF MAXIMUM STRENGTH
calcium carbonate, simethicone tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-0118 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D, CALCIUM CATION - UNII:2M83C4R6ZB) CALCIUM CARBONATE 750 mg DIMETHICONE, UNSPECIFIED (UNII: 92RU3N3Y1O) (DIMETHICONE, UNSPECIFIED - UNII:92RU3N3Y1O) DIMETHICONE, UNSPECIFIED 250 mg Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) YELLOW WAX (UNII: 2ZA36H0S2V) CARNAUBA WAX (UNII: R12CBM0EIZ) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) STARCH, CORN (UNII: O8232NY3SJ) CORN SYRUP (UNII: 9G5L16BK6N) DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3) FD&C BLUE NO. 2 ALUMINUM LAKE (UNII: 4AQJ3LG584) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C RED NO. 40 ALUMINUM LAKE (UNII: 6T47AS764T) FD&C YELLOW NO. 5 ALUMINUM LAKE (UNII: JQ6BLH9FR7) MALTODEXTRIN (UNII: 7CVR7L4A2D) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) 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) SOYBEAN LECITHIN (UNII: 1DI56QDM62) SUCROSE (UNII: C151H8M554) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CORN OIL (UNII: 8470G57WFM) Product Characteristics Color purple (Red) Score no score Shape ROUND Size 19mm Flavor BERRY (Mixed Berries, Strawberry) Imprint Code GT Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0067-0118-03 1 in 1 CARTON 02/03/2022 1 30 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:0067-0118-02 1 in 1 CARTON 02/03/2022 2 65 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:0067-0118-01 10 in 1 POUCH; Type 0: Not a Combination Product 02/03/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 02/03/2022 Labeler - Haleon US Holdings LLC (079944263)

