Label: EXTRA STRENGTH ANTACID- aluminum hydroxide and magnesium carbonate tablet, chewable
- NDC Code(s): 11673-814-00
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 7, 2024
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- Active ingredients (in each tablet)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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Principal Display Panel
NDC 11673-814-00
Compare to the active ingredients in Gaviscon® Extra Strength Antacid*
Extra Strength
Antacid Tablets
Aluminum Hydroxide
Magnesium Carbonate
- •
- Fast-Acting Heartburn Relief
- •
- Helps Keep Acid Down for Hours
Original Flavor
100 Chewable Tablets
WARNING: Consuming this product can expose you to chemicals including lead, which is known to the State of California to cause cancer. For more information, go to www.P65Warnings.ca.gov
Distributed by Target Corporation, Minneapolis, MN 55403
Made in U.S.A
TM & ©2020 Target Brands, Inc.
DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING
*This product is not manufactured or distributed by GlaxoSmithKline, the distributor of Gaviscon® Extra Strength Antacid.
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INGREDIENTS AND APPEARANCE
EXTRA STRENGTH ANTACID
aluminum hydroxide and magnesium carbonate tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-814 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) (ALUMINUM HYDROXIDE - UNII:5QB0T2IUN0) ALUMINUM HYDROXIDE 160 mg MAGNESIUM CARBONATE (UNII: 0E53J927NA) (CARBONATE ION - UNII:7UJQ5OPE7D) MAGNESIUM CARBONATE 105 mg Inactive Ingredients Ingredient Name Strength ALGINIC ACID (UNII: 8C3Z4148WZ) CALCIUM STEARATE (UNII: 776XM7047L) CORN SYRUP (UNII: 9G5L16BK6N) SODIUM BICARBONATE (UNII: 8MDF5V39QO) STARCH, CORN (UNII: O8232NY3SJ) SUCROSE (UNII: C151H8M554) Product Characteristics Color WHITE Score no score Shape ROUND Size 17mm Flavor BUTTERSCOTCH (Original) Imprint Code RP105 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-814-00 100 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 08/29/2019 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M001 08/29/2019 Labeler - TARGET CORPORATION (006961700)