Label: QUALITY CHOICE ULTRA STRENGTH ASSORTED FRUIT- calcium carbonate tablet, chewable
- NDC Code(s): 63868-048-72
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Official Label (Printer Friendly)
- Active ingredient (per tablet)
- Purpose
- Uses
- Warnings
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
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Package/Label Principal Display Panel
NDC 63868-048-72
Compare to Tums ®Ultra Strength active ingredient*
Ultra Strength
Antacid Tablets
Antacid Calcium Supplement
Calcium Carbonate 1000 mg
Relieves:
Upset Stomach
Heartburn
Acid Indigestion
Assorted Fruit
72 Chewable Tablets
K PAREVE
GLUTEN- FREE
QC SATISFACTION GURANTEED
©Distributed by C.D.M.A., Inc.,
43157 W. Nine Mile
Questions: 248-449-9300
*This product is not manufactured or distributed by GlaxoSmithKline LLC, the distributor of Tums®.
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE ULTRA STRENGTH ASSORTED FRUIT
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-048 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 1000 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) D&C RED NO. 27 (UNII: 2LRS185U6K) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) FD&C YELLOW NO. 6 (UNII: H77VEI93A8) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) Product Characteristics Color red, green, yellow, orange Score no score Shape ROUND Size 19mm Flavor FRUIT (assorted fruit) Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-048-72 72 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 04/18/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 04/18/2019 Labeler - CHAIN DRUG MARKETING ASSOCIATION (011920774)