Label: GAS RELIEF EXTRA STRENGTH- simethicone capsule, liquid filled
- NDC Code(s): 0363-0487-20, 0363-0487-50, 0363-0487-72
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated October 10, 2023
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- Active ingredient (in each softgel)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
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Principal Display Panel
EXTRA STRENGTH
Gas Relief
Simethicone 125 mg / Anti-Gas
Relieves:
- Bloating
- Pressure
- Discomfort
SOFTGELS
Compare to Gas-X® Extra Strength active ingredient‡‡
TAMPER EVIDENT: DO NOT USE IF CARTON IS OPENED OR IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
‡‡This product is not manufactured or distributed by Novartis, distributor Gas- X® Extra Strength
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
walgreens.com
- Product Label
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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:0363-0487 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 (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) PEPPERMINT OIL (UNII: AV092KU4JH) WATER (UNII: 059QF0KO0R) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) Product Characteristics Color green Score no score Shape OVAL Size 9mm Flavor Imprint Code PO;SCU;L125 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0487-72 72 in 1 CARTON 03/31/2016 02/28/2025 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0363-0487-20 20 in 1 CARTON 03/31/2016 02/28/2025 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0363-0487-50 50 in 1 CARTON 03/31/2016 02/28/2025 3 1 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 M016 03/31/2016 02/28/2025 Labeler - Walgreens (008965063)