Label: ULTRA STRENGTH- antacid tablets tablet, chewable
- NDC Code(s): 21130-031-72
- Packager: SAFEWAY
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 13, 2023
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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
NDC# 21130-031-72
*Compare to the active ingredient Ultra Strength Tums®
ULTRA STRENGTH
Antacid Tablets
Calcium Carbonate 1000 mg
Fast Relief of Upset Stomach, Heartburn, Acid Indigestion
Peppermint
Naturally and Artificially Flavored
GLUTEN FREE
72 Chewable Tablets
K PAREVE
Distributed by:
*This product is not manufactured or distributed by GlaxoSmithKline, owner of the registered trademark, Ultra Strength Tums®.
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INGREDIENTS AND APPEARANCE
ULTRA STRENGTH
antacid tablets tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:21130-031 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 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 19mm Flavor PEPPERMINT Imprint Code RP103 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:21130-031-72 72 in 1 BOTTLE; Type 0: Not a Combination Product 10/05/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 10/05/2020 Labeler - SAFEWAY (009137209)