Label: GOUT SYMPTOM FORMULA- natural medicine liquid
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Contains inactivated NDC Code(s)
NDC Code(s): 57955-6021-2 - Packager: King Bio Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
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
- Inactive Ingredient
- Dosage and Administration
- Purpose
- Warnings
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- Indications and Usage
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GOUT SYMPTOM FORMULA
natural medicine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-6021 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (AMMONIUM PHOSPHATE, DIBASIC - UNII:10LGE70FSU) AMMONIUM PHOSPHATE, DIBASIC 10 [hp_X] in 59 mL ATROPA BELLADONNA (UNII: WQZ3G9PF0H) (ATROPA BELLADONNA - UNII:WQZ3G9PF0H) ATROPA BELLADONNA 10 [hp_X] in 59 mL COLCHICUM AUTUMNALE BULB (UNII: 993QHL78E6) (COLCHICUM AUTUMNALE BULB - UNII:993QHL78E6) COLCHICUM AUTUMNALE BULB 10 [hp_X] in 59 mL FORMIC ACID (UNII: 0YIW783RG1) (FORMIC ACID - UNII:0YIW783RG1) FORMIC ACID 10 [hp_X] in 59 mL FRAXINUS EXCELSIOR LEAF (UNII: RC38362Q7M) (FRAXINUS EXCELSIOR LEAF - UNII:RC38362Q7M) FRAXINUS EXCELSIOR LEAF 10 [hp_X] in 59 mL LEDUM PALUSTRE TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) LEDUM PALUSTRE TWIG 10 [hp_X] in 59 mL SODIUM CARBONATE (UNII: 45P3261C7T) (SODIUM CATION - UNII:LYR4M0NH37) SODIUM CARBONATE 10 [hp_X] in 59 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 10 [hp_X] in 59 mL URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS 10 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-6021-2 59 mL in 1 BOTTLE, SPRAY Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 11/18/2011 Labeler - King Bio Inc. (617901350) Registrant - King Bio Inc. (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc. 617901350 manufacture