Label: QUALITY CHOICE EXTRA STRENGTH ASSORTED FRUIT- calcium carbonate tablet, chewable
- NDC Code(s): 63868-702-96
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 18, 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
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- presently taking a prescription drug. Antacids may interact with certain prescription drugs.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
NDC 63868-702-96
*Compare to the Active Ingredient in Extra Strength Tums®
EXTRA STRENGTH
Antacid Tablets
Calcium Carbonate 750 mg
Relieves:
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- Upset Stomach
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- Heartburn
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- Acid Indigestion
ASSORTED FRUIT
Naturally and Artificially Flavored
K PAREVE
96 Chewable Tablets
GLUTEN FREE
100% QC SATISFACTION GUARANTEED
Distributed by: C.D.M.A. Inc.©
43157 W 9 Mile Rd
Novi, MI 48375
Questions: 248-449-9300
*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Extra Strength Tums®
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE EXTRA STRENGTH ASSORTED FRUIT
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-702 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CALCIUM CARBONATE (UNII: H0G9379FGK) (CARBONATE ION - UNII:7UJQ5OPE7D) CALCIUM CARBONATE 750 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) D&C RED NO. 27 (UNII: 2LRS185U6K) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color YELLOW, GREEN, RED, ORANGE Score no score Shape ROUND Size 17mm Flavor FRUIT (lemon, orange, cherry, lime) Imprint Code RP102 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-702-96 96 in 1 BOTTLE; Type 0: Not a Combination Product 12/15/2018 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 12/15/2018 Labeler - CHAIN DRUG MARKETING ASSOCIATION (011920774)