Label: BEST CHOICE ULTRA STRENGTH (antacid tablets- calcium carbonate tablet, chewable
- NDC Code(s): 63941-031-16, 63941-031-72
- Packager: BEST CHOICE (VALU MERCHANDISERS COMPANY)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated July 15, 2025
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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.
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- Inactive ingredients
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Package/Label Principal Display Panel
*Compare to the active ingredient in Ultra Strength Tums ®
NDC# 63941-031-72
Best Choice®
ULTRA STRENGTH
Antacid Tablets
Calcium Carbonate 1000 mg
Fast Relief of
- Upset Stomach
- Heartburn
- Acid Indigestion
Assorted Berry Flavor
Naturally and Artificially Flavored
K PAREVE
GLUTEN FREE
72 Chewable Tablets
PROUDLY DISTRIBUTED BY:
ASSOCIATED WHOLESALE GROCERS, INC,
KANSAS CITY, KANSAS 66106
bestchoicebrand.com/66965
*This product is not manufactured or distributed by GlaxoSmithKline LLC, owner of the registered trademark, Ultra Strength Tums ®
Package Label for 72 Chewable tablets
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INGREDIENTS AND APPEARANCE
BEST CHOICE ULTRA STRENGTH
antacid tablets (calcium carbonate) tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:63941-031 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 pink, blue, pink (pink-blue) Score no score Shape ROUND Size 19mm Flavor BERRY (Assorted) Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:63941-031-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 10/04/2024 2 NDC:63941-031-16 160 in 1 BOTTLE; Type 0: Not a Combination Product 10/04/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 10/04/2024 Labeler - BEST CHOICE (VALU MERCHANDISERS COMPANY) (868703513)


