Label: GAS RELIEF EXTRA STRENGTH- simethicone capsule, liquid filled
-
NDC Code(s):
59726-897-10,
59726-897-15,
59726-897-20,
59726-897-30, view more59726-897-50, 59726-897-51
- Packager: P & L Development, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 30, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each softgel)
- Purpose
- Uses
- Warnings
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Principal Display Panel
Compare to the active ingredient in Gas-X® Extra Strength†
extra strength
gas relief
simethicone 125 mg
anti-gas
Relieves:
- Pressure
- bloating
- discomfort
softgels
†This product is not manufactured or distributed by GSK Consumer Healthcare, distributor of Gas-X® Extra Strength.
TAMPER EVIDENT: DO NOT USE IF BLISTER UNIT IS TORN, BROKEN OR SHOWS ANY SIGNS OF TAMPERING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by:
PL Developments
200 Hicks Street
Westbury, NY 11590
- Product Label
-
INGREDIENTS AND APPEARANCE
GAS RELIEF EXTRA STRENGTH
simethicone capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:59726-897 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) MANNITOL (UNII: 3OWL53L36A) Product Characteristics Color green Score no score Shape OVAL Size 9mm Flavor Imprint Code PO Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:59726-897-10 10 in 1 CARTON 07/31/2019 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:59726-897-51 150 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 07/31/2019 3 NDC:59726-897-15 15 in 1 CARTON 07/31/2019 3 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:59726-897-50 50 in 1 CARTON 07/31/2019 4 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:59726-897-30 30 in 1 CARTON 07/31/2019 5 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:59726-897-20 20 in 1 CARTON 07/31/2019 6 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 07/31/2019 Labeler - P & L Development, LLC (800014821)