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GAS RELIEF (Advance Pharmaceutical Inc.)

Available Formats

Dosage Form Package Information Links
TABLET, CHEWABLE 100 TABLET, CHEWABLE in 1 BOTTLE (17714-019-01) Label Information

Complete GAS RELIEF Information

  • Drug Facts

    .


  • Active Ingredient

    (in each chewable tablet)

    Simethicone 80 mg


  • Purpose

    Antiflatulent


  • Uses

    relieves

    • bloating
    • pressure
    • discomfort of gas which can be caused by certain foods or air swallowing

  • Warnings

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


  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children


  • Directions

    • chew thoroughly 1 to 2 tablets as needed after meals and at bed time.
    • do not exceed 6 tablets per day unless directed by a physician

  • Other Information

    • store at room temperature 15-30 °C (59-86 °F)
    • protect from moisture

  • Inactive Ingredients

    dextrose, dipac sugar, maltodextrin, peppermint flavor, sorbitol, stearic acid


  • Questions or Comments

    TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING

    Call 631-981-4600, 8.30 am – 4.30 pm EST Monday - Friday


  • Package Label

    7bf77325-figure-01

    NDC: 17714-019-01  – 100 CHEWABLE TABLETS


  • INGREDIENTS AND APPEARANCE
    GAS RELIEF 
    simethicone tablet, chewable
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:17714-019
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    DIMETHICONE (UNII: 92RU3N3Y1O) (DIMETHICONE - UNII:92RU3N3Y1O) DIMETHICONE 80 mg
    Inactive Ingredients
    Ingredient Name Strength
    DEXTROSE (UNII: IY9XDZ35W2)  
    SUCROSE (UNII: C151H8M554)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    PEPPERMINT (UNII: V95R5KMY2B)  
    SORBITOL (UNII: 506T60A25R)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    Product Characteristics
    Color WHITE Score no score
    Shape ROUND Size 13mm
    Flavor PEPPERMINT Imprint Code AP;019
    Contains     
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:17714-019-01 100 in 1 BOTTLE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    OTC monograph final part332 11/04/1999
    Labeler - Advance Pharmaceutical Inc. (078301063)
    Registrant - Advance Pharmaceutical Inc. (078301063)
    Establishment
    Name Address ID/FEI Business Operations
    Advance Pharmaceutical Inc. 078301063 MANUFACTURE(17714-019)