Label: GAS RELIEF ULTRA STRENGTH- simethicone capsule, liquid filled
- NDC Code(s): 80136-792-01
- Packager: NORTHEAST PHARMA (Heartland Pharma)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 11, 2024
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- Active ingredient (in each softgel)
- Purpose
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- Inactive ingredients
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Compare to active ingredient in PHAZYME® ULTRA STRENGTH†
Ultra Strength
GAS RELIEF
Simethicone, 180 mg | Antigas
Fast relief of:
- Gas
- Pressure
- Bloating
- Discomfort
Softgels
**This product is not manufactured or distributed by C.B. Fleet Company Inc., distributor of Phazyme® Ultra Strength.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by: NORTHEAST PHARMA
South Burlington, VT 05403
- Package Label
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INGREDIENTS AND APPEARANCE
GAS RELIEF ULTRA STRENGTH
simethicone capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:80136-792 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 180 mg Inactive Ingredients Ingredient Name Strength FD&C YELLOW NO. 6 (UNII: H77VEI93A8) GELATIN (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) FD&C RED NO. 40 (UNII: WZB9127XOA) Product Characteristics Color orange Score no score Shape OVAL Size 12mm Flavor Imprint Code 05A Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:80136-792-01 60 in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 06/25/2021 06/25/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M002 06/25/2021 06/25/2025 Labeler - NORTHEAST PHARMA (Heartland Pharma) (081232935)