Label: GOUT SYMPTOM RELIEF- ammon phos, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica and urtica urens. liquid
- NDC Code(s): 57955-9975-2
- 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 March 6, 2026
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
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Active ingredients
Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies.
Ammon phos, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum, Nux vomica and Urtica urens.
** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″
- INDICATIONS & USAGE
-
Questions
Gout Symptom Relief
Dr. King's Natural Medicine
Taste free, Pure Water Base
HOMEOPATHIC 2 fl oz (59 mL)
Oral Spray Gluten Free
*Less than 1% Alcohol. Tamper evident for your protection.
King Bio • 3 Westside Drive, Asheville, NC 28806 USA
www.DrKings.com
for additional information.Dr. King's FREE Videos and Home
Healing Techniques to integrate with
this product and optimize your
healing experience. - Warnings
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- Inactive Ingredients
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PURPOSE
Equal volumes of each HPUS** ingredient in 10X, 30X, and 1LM potencies.
Active ingredients Purpose †
Ammon phos ...........................inflammation of joints
Belladonna................................red and tender joints
Colchicum autumnale ...................sensitivity to touch
Formicum acidum.............................joint discomfort
Fraxinus excelsior..................foot-related discomforts
Ledum palustre..................swelling of joints and toesNatrum carbonicum ..............................tender joints
Nux vomica...................................................itching
Urtica urens .....................................joint discomfort** "The designation 'HPUS’ means that the active ingredient(s) in this product complies with a monograph (or Monographs) in the Homeopathic Pharmacopeia of the United States.″
† Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated. - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
GOUT SYMPTOM RELIEF
ammon phos, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica and urtica urens. liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:57955-9975 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength AMMONIUM PHOSPHATE, DIBASIC (UNII: 10LGE70FSU) (PHOSPHATE ION - UNII:NK08V8K8HR) 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 BARK (UNII: R6KCX5H8I2) (FRAXINUS EXCELSIOR BARK - UNII:R6KCX5H8I2) FRAXINUS EXCELSIOR BARK 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 RHODODENDRON TOMENTOSUM LEAFY TWIG (UNII: 877L01IZ0P) (LEDUM PALUSTRE TWIG - UNII:877L01IZ0P) RHODODENDRON TOMENTOSUM LEAFY TWIG 10 [hp_X] in 59 mL SODIUM CARBONATE (UNII: 45P3261C7T) (CARBONATE ION - UNII:7UJQ5OPE7D) 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 WHOLE (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS WHOLE 10 [hp_X] in 59 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) POTASSIUM SORBATE (UNII: 1VPU26JZZ4) WATER (UNII: 059QF0KO0R) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:57955-9975-2 59 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product 03/10/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 03/10/2026 Labeler - King Bio Inc. (617901350) Registrant - King Bio Inc. (617901350) Establishment Name Address ID/FEI Business Operations King Bio Inc. 617901350 manufacture(57955-9975) , api manufacture(57955-9975)
