Label: GOUT SYMPTOM FORMULA- natural medicine liquid

  • Category: HUMAN OTC DRUG LABEL

DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

Drug Label Information

Updated November 18, 2011

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  • Active Ingredients

    Official HPUS

    Ammonium Phosphoricum, Belladonna, Colchicum Autumnale, Formicum Acidum, Fraxinus Excelsior, Ledum Palustre, Natrum Carbonicum, Nux Vomica, and Urtica Urens.

    Reference image gout.jpg

  • Inactive Ingredient


    Equal volumes of each ingredient in a Bio-Energetically Enhanced pure water base. 10X, 30X, and LM1 potencies.

    Reference image gout.jpg
  • Dosage and Administration

    Directions Initially, depress pump until primed. Hold close to mouth and spray one dose directly into mouth. Use 3 times per day. Use additionally as needed.

    Adult Dose: 3 pump sprays

    Children: (2-12 years) 2 pump sprays

    Reference image gout.jpg


  • Purpose

    For Temporary relief of pain in the foot, heel, toes and joints including: swelling, burning, itching, tingling, tearing pains, throbbing, cramps, shooting pains.

    Reference image gout.jpg

  • Warnings

    If symptoms persist or worsen, or if pregnant or nursing, take only on advice of a healthcare professional. Keep out of reach of children.

    Other: Tamper resistant for your protection. Use only if safety seal is intact.

    Reference image gout.jpg

  • KEEP OUT OF REACH OF CHILDREN


    Keep out of reach of children.

    Reference image gout.jpg


  • Indications and Usage

    Uses for temporary relief of pain in the foot, heel, toes and joints including:

    • swelling
    • burning
    • itching
    • tingling
    • tearing pains
    • throbbing
    • cramps
    • shooting pains
    Reference image gout.jpg
  • PRINCIPAL DISPLAY PANEL

    Image of label


    King Bio Inc.

    3 Westside Drive

    Asheville, NC 28806

    www.kingbio.com

    Questions? Call 800.543.3245

  • INGREDIENTS AND APPEARANCE
    GOUT SYMPTOM FORMULA 
    natural medicine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57955-6021
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (AMMONIUM PHOSPHATE, DIBASIC - UNII:10LGE70FSU) AMMONIUM PHOSPHATE, DIBASIC10 [hp_X]  in 59 mL
    ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA10 [hp_X]  in 59 mL
    COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6) COLCHICUM AUTUMNALE BULB10 [hp_X]  in 59 mL
    FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1) FORMIC ACID10 [hp_X]  in 59 mL
    FRAXINUS EXCELSIOR LEAF (UNII: RC38362Q7M) (FRAXINUS EXCELSIOR LEAF - UNII:RC38362Q7M) FRAXINUS EXCELSIOR LEAF10 [hp_X]  in 59 mL
    LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) LEDUM PALUSTRE TWIG10 [hp_X]  in 59 mL
    SODIUM CARBONATE (UNII: 45P3261C7T) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CARBONATE10 [hp_X]  in 59 mL
    STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED10 [hp_X]  in 59 mL
    URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS10 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57955-6021-259 mL in 1 BOTTLE, SPRAY
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/18/2011
    Labeler - King Bio Inc. (617901350)
    Registrant - King Bio Inc. (617901350)
    Establishment
    NameAddressID/FEIBusiness Operations
    King Bio Inc. 617901350manufacture
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