Label: MEIJER EXTRA STRENGTH TROPICAL FRUIT- calcium carbonate tablet, chewable
- NDC Code(s): 41250-203-20
- Packager: MEIJER DISTRIBUTION INC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 28, 2023
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- 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 drug.
- Directions
- Other information
- Inactive ingredients
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Compare to Extra Strength Tums® active ingredient*
meijer®
NDC# 41250-203-20
antacid tablets
Calcium Carbonate 750 mg
Extra Strength
Tropical Fruit Flavors
Naturally and Artificially Flavored
Fast Relief of Upset Stomach, Heartburn and Acid Indigestion
200 CHEWABLE TABLETS
GLUTEN-FREE
OUR QUALITY GUARANTEED
WWW.MEIJER.COM/SATISFACTION
K PAREVE
DIST. BY MEIJER DISTRIBUTION, INC
GRAND RAPIDS, MI 49544
www.meijer.com
*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Tums®.
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INGREDIENTS AND APPEARANCE
MEIJER EXTRA STRENGTH TROPICAL FRUIT
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-203 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 750 mg Inactive Ingredients Ingredient Name Strength ADIPIC ACID (UNII: 76A0JE0FKJ) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C RED NO. 40 (UNII: WZB9127XOA) 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, ORANGE, WHITE, RED Score no score Shape ROUND Size 17mm Flavor FRUIT (banana, orange, pineapple, tropical fruit punch) Imprint Code RP102 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-203-20 200 in 1 BOTTLE; Type 0: Not a Combination Product 03/29/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 03/29/2019 Labeler - MEIJER DISTRIBUTION INC (006959555)