Label: ULTRA STRENGTH ANTACID ASSORTED BERRIES- calcium carbonate tablet, chewable
- NDC Code(s): 49035-803-16, 49035-803-27, 49035-803-72
- Packager: WAL-MART STORES INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 14, 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
- Other information
- Inactive ingredients
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Package/Label Principal Display Panel
Compare To Tums® Ultra Strength active ingredient*
ULTRA STRENGTH
Antacid Tablets
Calcium Carbonate 1000 mg
Fast Relief of:
- •
- Upset Stomach
- •
- Acid Indigestion
- •
- Heartburn
Assorted Berries
Naturally and Artificially Flavored
CHEWABLE TABLETS
1000 mg
K PAREVE
Gluten-Free
Satisfaction guaranteed- or we’ll replace it or give you your money back. For questions or comments.
Please call 1-888-287-1915
Distributed By: Walmart Stores, Inc.
Bentonville, AR 72716
*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength Tums®.
Package Label for 160 Chewable Tablets
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INGREDIENTS AND APPEARANCE
ULTRA STRENGTH ANTACID ASSORTED BERRIES
calcium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49035-803 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) DEXTROSE, UNSPECIFIED FORM (UNII: IY9XDZ35W2) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) STARCH, CORN (UNII: O8232NY3SJ) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color RED, PINK, PURPLE, BLUE Score no score Shape ROUND Size 19mm Flavor BERRY (Assorted Berries) Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49035-803-27 160 in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2019 2 NDC:49035-803-16 160 in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2019 3 NDC:49035-803-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 04/09/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 04/09/2019 Labeler - WAL-MART STORES INC. (051957769)