Label: GAS RELIEF EXTRA STRENGTH- simethicone capsule, liquid filled
- NDC Code(s): 11673-550-50, 11673-550-72
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 16, 2023
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- Active ingredient (in each softgel)
- Purpose
- Uses for the relief
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
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Compare to active ingredient in Extra Strength Gas-X® Softgels*
Extra Strength
Gas Relief
Simethicone softgels 125 mg/ antigas
fast relief of gas pressure, bloating and discomfort
easy to swallow
up & up
DO NOT USE IF ANY INDIVIDUAL BLISTER IS BROKEN OR OPEN.
IMPORTANT: Keep this carton for future reference on full labeling
**This product is not manufactured or distributed by GSK Consumer Healthcare, Inc. the distributor of Gas-X® Extra Strength Softgels.
Distributed by Target Corporation
Minneapolis, MN 55403
TM & © 2021 Target Brands, Inc.
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This product offers fast, effective relief of pressure and bloating that antacids can’t provide.
They are specially formulated with simethicone, the antigas medicine doctors recommends most for pressure, bloating or discomfort referred to as gas.
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INGREDIENTS AND APPEARANCE
GAS RELIEF EXTRA STRENGTH
simethicone capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-550 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 125 mg Inactive Ingredients Ingredient Name Strength D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) PEPPERMINT OIL (UNII: AV092KU4JH) WATER (UNII: 059QF0KO0R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color GREEN Score no score Shape OVAL Size 9mm Flavor Imprint Code PO;S1;SCU Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-550-50 5 in 1 CARTON 08/30/2013 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:11673-550-72 6 in 1 CARTON 08/30/2013 2 12 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M002 08/30/2013 Labeler - Target Corporation (006961700)