Label: QUALITY CHOICE REGULAR STRENGTH PEPPERMINT FLAVOR- calcium carbonate tablet, chewable
- NDC Code(s): 63868-700-15
- Packager: CHAIN DRUG MARKETING ASSOCIATION
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated December 18, 2024
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- Download DRUG LABEL INFO: PDF XML
- 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
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
NDC#63868-700-15
*Compare to the Active Ingredient in Regular Strength Tums ®
REGULAR STRENGTH
Antacid Tablets
CALCIUM CARBONATE 500mg
Relieves:
- Upset Stomach
- Heartburn
- Acid Indigestion
Peppermint
Naturally and Artificially Flavored
100% QC SATISFACTION GUARANTEED
GLUTEN FREE
150 CHEWABLE TABLETS
K PAREVE
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, Regular Strength Tums ®.
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INGREDIENTS AND APPEARANCE
QUALITY CHOICE REGULAR STRENGTH PEPPERMINT FLAVOR
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63868-700 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 500 mg Inactive Ingredients Ingredient Name Strength DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color white Score no score Shape ROUND Size 17mm Flavor PEPPERMINT Imprint Code RP101 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63868-700-15 150 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)