Label: GOOD SENSE GAS RELIEF- simethicone capsule, liquid filled

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated September 30, 2024

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  • Active ingredient (in each softgel)

    Simethicone 180 mg

  • Purpose

    Anti-gas

  • Use

    •
    relieves bloating, pressure or fullness commonly referred to as gas
  • Warnings

    Stop use and ask a doctor if

    condition persists

    Keep out of reach of children.

  • Directions

    •
    swallow one or two softgels as needed after a meal
    •
    do not exceed two softgels per day except under the advice and supervision of a physician
  • Other information

    •
    each softgel contains: potassium 5 mg
    •
    store at 68°-77°F (20°-25°C)
  • Inactive ingredients

    FD&C red no. 40, FD&C yellow no. 6, gelatin, glycerin

  • Questions or comments?

    1-800-719-9260

  • Principal Display Panel

    GOODSENSE®

    Ultra Strength

    Gas Relief

    Anti-Gas

    Simethicone 180 mg

    Actual Size

    Relieves Gas Fast

    ● Pressure

    ● Bloating

    ● Discomfort

    Easy to Swallow

    Compare to active ingredient of Ultra Strength Phazyme®

    60 Softgels (180 mg)

    Gas Relief Carton
  • INGREDIENTS AND APPEARANCE
    GOOD SENSE GAS RELIEF 
    simethicone capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0113-0657
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE180 mg
    Inactive Ingredients
    Ingredient NameStrength
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    FD&C RED NO. 40 (UNII: WZB9127XOA)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    GELATIN, UNSPECIFIED (UNII: 2G86QN327L)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Product Characteristics
    ColorORANGEScoreno score
    ShapeOVALSize9mm
    FlavorImprint Code L657
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:0113-0657-721 in 1 CARTON04/05/2002
    160 in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00204/05/2002
    Labeler - L. Perrigo Company (006013346)
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