Label: GAS RELIEF SIMETHICONE 180MG SOFTGEL- simethicone capsule, liquid filled

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated July 18, 2024

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  • Active Ingredient (in each softgel)

    Simethicone 180 mg

  • Purpose

    Antiflatulent (Antigas)

  • Uses

    relieves

    • bloating
    • pressure
    • fullness commonly referred to as gas
  • Warnings

    Stop use and ask a doctor if condition persists.

    If pregnant or breast-feeding, ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN

    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

    • store at 15° to 30°C (59° to 86°F)
  • Inactive Ingredients

    Peppermint oil, Gelatin, Sorbitol, sorbitan anhydrous, Glycerin, Titanium dioxide, FD &C yellow 6/sunset yellow, Black iron oxide.

  • Questions or Comments?

    Call 1 (718) 337-8733 or visit support@nuvicare.com

  • PRINCIPAL DISPLAY PANEL

    PL0214-00 NC-Gas Relief 180mg-100ct

  • INGREDIENTS AND APPEARANCE
    GAS RELIEF SIMETHICONE 180MG SOFTGEL 
    simethicone capsule, liquid filled
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84324-015
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE180 mg
    Inactive Ingredients
    Ingredient NameStrength
    PEPPERMINT OIL (UNII: AV092KU4JH)  
    GELATIN (UNII: 2G86QN327L)  
    SORBITOL (UNII: 506T60A25R)  
    SORBITAN (UNII: 6O92ICV9RU)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    FD&C YELLOW NO. 6 (UNII: H77VEI93A8)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    Product Characteristics
    ColororangeScoreno score
    ShapeOVALSize11mm
    FlavorImprint Code 910
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84324-015-01100 in 1 BOTTLE; Type 0: Not a Combination Product07/18/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM00207/18/2024
    Labeler - NUVICARE LLC (119257565)
    Registrant - NUVICARE LLC (119257565)
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