![TUMS CHEWY BITES WITH GAS RELIEF (CALCIUM CARBONATE AND SIMETHICONE) TABLET, CHEWABLE [GLAXOSMITHKLINE CONSUMER HEALTHCARE HOLDINGS (US) LLC]](https://medic.hrt.org//dailymed/images/6d7be7e4-4bff-4cfd-bbbe-df412ac9db10/106111XA_TUMS Chewy Bites with Gas_26 ct.JPG.jpg.jpg.jpg.jpg.jpg)
| NDC | 0135-0624-01, 0135-0624-02 |
| Set ID | 6d7be7e4-4bff-4cfd-bbbe-df412ac9db10 |
| Category | HUMAN OTC DRUG LABEL |
| Packager | GlaxoSmithKline Consumer Healthcare Holdings (US) LLC |
| Generic Name | |
| Product Class | |
| Product Number | |
| Application Number | PART331 |
- Active ingredient (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
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Inactive ingredients
alcohol, ammonium hydroxide, beeswax, caprylic/capric triglycerides, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethanol, ethyl acetate, ethyl alcohol, FD&C blue #1 alum lake, FD&C red #40, FD&C red #40 alum lake, FD&C yellow #5 alum lake (tartrazine), FD&C yellow #6 alum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methylparaben, modified corn starch, n-butyl alcohol, phosphoric acid, propylene glycol, propylparaben, purified water, PVP, shellac, sodium benzoate, sorbic acid, sorbitol, soy bean oil, soy lecithin, sucrose, TBHQ, titanium dioxide
- Questions or comments?
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Principal Display Panel
NEW
NDC 0135-0624-01
TUMS® with Gas Relief
CALCIUM CARBONATE / SIMETHICONE
ANTACID/ANTIGAS
Chewy Bites
Lemon & Strawberry
FAST RELIEF OF HEARTBURN & GAS
28 CHEWABLE TABLETS
Safety sealed – Do not use if printed inner seal beneath cap is missing or broken.
Trademarks are owned by or licensed to the GSK group of companies.
Distributed by:
GSK Consumer Healthcare
Warren, NJ 07059
©2016 GSK or its licensor
106111XA
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INGREDIENTS AND APPEARANCE
TUMS CHEWY BITES WITH GAS RELIEF
calcium carbonate and simethicone tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0135-0624 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CALCIUM CATION - UNII:2M83C4R6ZB, CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 750 mg DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg Inactive Ingredients Ingredient Name Strength SILICON DIOXIDE (UNII: ETJ7Z6XBU4) ALCOHOL (UNII: 3K9958V90M) AMMONIA (UNII: 5138Q19F1X) YELLOW WAX (UNII: 2ZA36H0S2V) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) CARNAUBA WAX (UNII: R12CBM0EIZ) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) COCONUT OIL (UNII: Q9L0O73W7L) STARCH, CORN (UNII: O8232NY3SJ) CORN SYRUP (UNII: 9G5L16BK6N) ICODEXTRIN (UNII: 2NX48Z0A9G) ETHYL ACETATE (UNII: 76845O8NMZ) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) 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) MODIFIED CORN STARCH (1-OCTENYL SUCCINIC ANHYDRIDE) (UNII: 461P5CJN6T) BUTYL ALCOHOL (UNII: 8PJ61P6TS3) PHOSPHORIC ACID (UNII: E4GA8884NN) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) PROPYLPARABEN (UNII: Z8IX2SC1OH) WATER (UNII: 059QF0KO0R) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) SHELLAC (UNII: 46N107B71O) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBIC ACID (UNII: X045WJ989B) SORBITOL (UNII: 506T60A25R) SOYBEAN OIL (UNII: 241ATL177A) LECITHIN, SOYBEAN (UNII: 1DI56QDM62) SUCROSE (UNII: C151H8M554) TERT-BUTYLHYDROQUINONE (UNII: C12674942B) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color RED (red, yellow) Score no score Shape ROUND Size 19mm Flavor STRAWBERRY (Strawberry, Lemon) Imprint Code T Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0135-0624-01 28 in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2018 2 NDC:0135-0624-02 54 in 1 BOTTLE; Type 0: Not a Combination Product 03/01/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC monograph final part331 03/01/2018 Labeler - GlaxoSmithKline Consumer Healthcare Holdings (US) LLC (079944263)
