Label: TUMS CHEWY BITES- calcium carbonate tablet, chewable
- NDC Code(s): 67751-191-01
- Packager: Navajo Manufacturing Company Inc.
- This is a repackaged label.
- Source NDC Code(s): 0135-0618
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated April 15, 2024
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- Official Label (Printer Friendly)
- Active ingredient (per tablet)
- Purpose
- 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 INGREDIENT
Acacia gum, alcohol, ammonium hydroxide, beeswax, carmine, carnauba wax, citric acid, coconut oil, corn starch, corn syrup, dextrin, ethyl acetate, ethyl alcohol, FD&C blue #1 alum lake, FD&C blue #2 alum lake, FD&C red #40 alum lake, FD&C yellow #6 alum lake, flavors, gum arabic, isopropyl alcohol, maltodextrin, methylparaben, n-butyl alcohol, phosphoric acid, propylparaben, propylene glycol, purified water, shellac, sorbic acid, sorbitol, soybean oil, soy lecithin, sucrose, TBHQ, titanium dioxide, vegetable oil
- Questions?
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Principal Display Panel
Handy Solutions® Guarantee If dissatisfied with this product, return it with a brief explanation to 5330 Fox Street, Denver, CO 80216. We'll replace it free of charge and refund your postage. You may also call 1-800-525-5097 for customer service, 9am to 4pm MST, weekdays or email us at customerservice@navajoinc.com.
Visit us on the web at www.navajoinc.comPackaged and Distributed by
Navajo Mfg. Co. Inc. with permission
of GSK Consumer Healthcare
©2019 GSK group of companies
or its licensor.
All rights reserved.
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INGREDIENTS AND APPEARANCE
TUMS CHEWY BITES
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67751-191(NDC:0135-0618) 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 Inactive Ingredients Ingredient Name Strength ACACIA (UNII: 5C5403N26O) ALCOHOL (UNII: 3K9958V90M) AMMONIA (UNII: 5138Q19F1X) YELLOW WAX (UNII: 2ZA36H0S2V) CARMINIC ACID (UNII: CID8Z8N95N) 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) ALUMINUM OXIDE (UNII: LMI26O6933) FD&C BLUE NO. 2 (UNII: L06K8R7DQK) FD&C RED NO. 40 (UNII: WZB9127XOA) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) ISOPROPYL ALCOHOL (UNII: ND2M416302) MALTODEXTRIN (UNII: 7CVR7L4A2D) METHYLPARABEN (UNII: A2I8C7HI9T) BUTYL ALCOHOL (UNII: 8PJ61P6TS3) PHOSPHORIC ACID (UNII: E4GA8884NN) PROPYLPARABEN (UNII: Z8IX2SC1OH) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SHELLAC (UNII: 46N107B71O) 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) CORN OIL (UNII: 8470G57WFM) Product Characteristics Color purple Score no score Shape ROUND Size 19mm Flavor RASPBERRY (Mixed berry: Raspberry and Blueberry) Imprint Code T Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67751-191-01 1 in 1 CARTON 05/30/2019 1 2 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 05/30/2019 Labeler - Navajo Manufacturing Company Inc. (091917799) Establishment Name Address ID/FEI Business Operations Navajo Manufacturing Company Inc. 136941411 relabel(67751-191)