Label: GAS-X TOTAL RELIEF MAXIMUM STRENGTH- calcium carbonate, simethicone tablet, chewable
- NDC Code(s): 0067-0119-01
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 5, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredients (per tablet)
- Purpose
- Uses
-
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
-
Inactive ingredients
alcohol, ammonium hydroxide, beeswax, carnauba wax, citric acid, corn syrup, dextrin, ethyl acetate, FD&C yellow 6, FD&C yellow 6 lake, flavor, gum arabic, isopropyl alcohol, maltodextrin, methylparaben, n-butyl alcohol, pharmaceutical ink, phosphoric acid, propylene glycol, propylparaben, purified water, shellac, sorbic acid, sorbitol, soy lecithin, sucrose, titanium dioxide, vegetable oil (coconut origin)
- Questions or comments?
- Additional Information
- Principal Display Panel
-
INGREDIENTS AND APPEARANCE
GAS-X TOTAL RELIEF MAXIMUM STRENGTH
calcium carbonate, simethicone tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0067-0119 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 (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 250 mg Inactive Ingredients Ingredient Name Strength 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 YELLOW NO. 6 (UNII: H77VEI93A8) ALUMINUM OXIDE (UNII: LMI26O6933) 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) SORBIC ACID (UNII: X045WJ989B) SORBITOL (UNII: 506T60A25R) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SUCROSE (UNII: C151H8M554) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) CORN OIL (UNII: 8470G57WFM) Product Characteristics Color purple Score no score Shape ROUND Size 19mm Flavor BERRY (Mixed Berries) Imprint Code GT Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0067-0119-01 2 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)