Label: QC ANTACID CALCIUM ASSORTED BERRY- calcium carbonate tablet, chewable
- NDC Code(s): 63868-049-72
- Packager: CHAIN DRUG MARKETING ASSOCIATION INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2024
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- Active ingredient (per tablet)
- Purpose
- Uses
- Warnings
- Ask a doctor or pharmacist before use if you are
- When using this product
- Keep out of reach of children.
- Directions
- Inactive ingredients
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Package/Label Principal Display Panel
QUALITY CHOICE®
NDC# 63868-049-72
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 Berry
GLUTEN FREE
72 CHEWABLE TABLETS
K PAREVE
QC SATISFACTION GURANTEED
©Distributed by: C.D.M.A., Inc.
43157 W Nine Mile
Novi, MI 48376-0995
Questions: 248-449-9300
*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of Tums®.
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INGREDIENTS AND APPEARANCE
QC ANTACID CALCIUM ASSORTED BERRY
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-049 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 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) FD&C RED NO. 40 (UNII: WZB9127XOA) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color PINK (blue-pink) , BLUE Score no score Shape ROUND Size 17mm Flavor BERRY (assorted berry) Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-049-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 04/16/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 04/16/2019 Labeler - CHAIN DRUG MARKETING ASSOCIATION INC. (011920774)