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GAMMA -12 (Guna spa)

Available Formats

Dosage Form Package Information Links
SOLUTION/ DROPS 1 BOTTLE, DROPPER in 1 BOX (17089-405-18) > 30 mL in 1 BOTTLE, DROPPER Label Information

Complete GAMMA -12 Information

  • ACTIVE INGREDIENTS/PURPOSE

    INTERFERON GAMMA    4C    IMMUNE SUPPORT
    INTERLEUKIN-12    4C    IMMUNE SUPPORT


  • USES

    For the temporary relief of upper respiratory symptoms due to hay fever or airborne allergies such as: -Cough –Airway irritation –Shortness of breath


  • WARNINGS

    Stop use and ask doctor if symptoms of cough, shortness of breath, or wheezing do not improve, worsen or persist more than 3 days


  • PREGNANCY

    If pregnant or breast-feeding ask a doctor before use


  • WARNINGS

    Keep this and all medicines out of reach of children


  • DIRECTIONS

    Take 15 minutes before meals

    Adults and children 12 years and older

    20 drops in a little water, 2 times per day

    Children between 12 years and 6 years of age

    10 drops in a little water, 2 times per day

    Children under 6 years

    5 drops in a glass of water, 2 times per day


  • QUESTIONS

    Questions?: info@gunainc.com
    tel. (484) 223-3500


  • INACTIVE INGREDIENT

    inactive ingredient: Ethyl alcohol 30%.


  • INDICATIONS & USAGE

    take 15 minutes before meals


  • PRINCIPAL DISPLAY PANEL

    image of box label


  • INGREDIENTS AND APPEARANCE
    GAMMA -12 
    interleukin-12 human recombinant - interferon gamma-1b - solution/ drops
    Product Information
    Product Type HUMAN OTC DRUG Item Code (Source) NDC:17089-405
    Route of Administration ORAL
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    INTERFERON GAMMA-1B (UNII: 21K6M2I7AG) (INTERFERON GAMMA-1B - UNII:21K6M2I7AG) INTERFERON GAMMA-1B 4 [hp_C]  in 30 mL
    INTERLEUKIN-12 HUMAN RECOMBINANT (UNII: 02FXP10O2U) (INTERLEUKIN-12 HUMAN RECOMBINANT - UNII:02FXP10O2U) INTERLEUKIN-12 HUMAN RECOMBINANT 4 [hp_C]  in 30 mL
    Inactive Ingredients
    Ingredient Name Strength
    ALCOHOL (UNII: 3K9958V90M) 9 mL  in 30 mL
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:17089-405-18 1 in 1 BOX 03/31/2011
    1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 04/29/2010
    Labeler - Guna spa (430538264)
    Establishment
    Name Address ID/FEI Business Operations
    Guna spa 338587646 manufacture(17089-405)