GOUT SYMPTOM RELIEF- ammon phos, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica and urtica urens. liquid

Gout Symptom Relief by

Drug Labeling and Warnings

Gout Symptom Relief by is a Homeopathic medication manufactured, distributed, or labeled by King Bio Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

Uses † temporary relief of symptoms in toes, heels, feet, or joints:

• discomforts
• cramping
• tender or itchy joints

 † Claims based on traditional Homeopathic practice, not accepted medical evidence, not
FDA evaluated.

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

• Stop use and consult a doctor if symptoms worsen or persist for more than 7 days.
• If pregnant or breast-feeding, ask a healthcare professional before use.

KEEP OUT OF REACH OF CHILDREN

• Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center immediately.

DOSAGE & ADMINISTRATION

• Directions: Oral Dose
• Adults and Children over 12:
  • 2 sprays into mouth 3 to 6 times per day
• Children 6-12:
  • 1 spray into mouth 3 to 6 times per day
• Children under 6:
  • Do not use in children under 6, unless directed to by a doctor

OTHER SAFETY INFORMATION

Other information

Tamper evident for your protection. Use only if safety seal is intact.

Inactive Ingredients

Citric acid, Potassium sorbate, and USP purified water.

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 toes

Natrum 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

INGREDIENTS AND APPEARANCE

GOUT SYMPTOM RELIEF 
ammon phos, belladonna, colchicum autumnale, formicum acidum, fraxinus excelsior, ledum palustre, natrum carbonicum, nux vomica and urtica urens. liquid

Product 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)