FDA.reportPublic FDA data

Gout Symptom Relief

Manufacturer
King Bio Inc.
Effective date
2026-03-06
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:37:53

Label at a glance#

ProductGout Symptom Relief
Active ingredientAMMONIUM PHOSPHATE, DIBASIC, ATROPA BELLADONNA, COLCHICUM AUTUMNALE BULB, FORMIC ACID, FRAXINUS EXCELSIOR BARK, FRAXINUS EXCELSIOR LEAF, RHODODENDRON TOMENTOSUM LEAFY TWIG, SODIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, URTICA URENS WHOLE
Label structure10 sections

Label contents#

Full prescribing information#

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

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 SECTION

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

OTC - QUESTIONS SECTION

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

WARNINGS SECTION

  • 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.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DOSAGE & ADMINISTRATION SECTION

DirectionsOral 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

INACTIVE INGREDIENT SECTION

Citric acid, Potassium sorbate, and USP purified water.

OTC - PURPOSE SECTION

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.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Gout Symptom Relief.jpgGout Symptom Relief.jpg

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codedrkings.com/Gout Symptom Relief.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
e2db08c6-133f-4f4f-afb4-e90a2418d6f6Product name120230320
ce6d5c06-3ae0-18a6-d5b3-8cd3cc0f8906Product name720210625
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
11ed6f83-cdd2-4637-8379-b1a1d3ae3cdeProduct name120181101
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
86c45a79-b9f0-4476-a27c-6e10db098497Product name120180125
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
57955-9975-2Gout Symptom Relief59 mL in 1 BOTTLE, SPRAYLIQUID591

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-997557955-9975-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 13 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIUM PHOSPHATE, DIBASIC10LGE70FSUACTIB
ATROPA BELLADONNAWQZ3G9PF0HACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
FORMIC ACID0YIW783RG1ACTIB
FRAXINUS EXCELSIOR BARKR6KCX5H8I2ACTIB
FRAXINUS EXCELSIOR LEAFRC38362Q7MACTIB
RHODODENDRON TOMENTOSUM LEAFY TWIG877L01IZ0PACTIB
SODIUM CARBONATE45P3261C7TACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
URTICA URENS WHOLEIHN2NQ5OF9ACTIB
ANHYDROUS CITRIC ACIDXF417D3PSLIACT
POTASSIUM SORBATE1VPU26JZZ4IACT
WATER059QF0KO0RIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Gout Symptom ReliefAMMON PHOS, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA AND URTICA URENS.King Bio Inc.41dc03fc-169b-4691-bd62-9a41d7a6d2f72026-03-06WarningsExact identifier
ndc (package): 57955-9975-2
ndc (product): 57955-9975
ndc11 (package): 57955997502
spl id: 4590e343-960e-4fa7-888e-8b9ed5ad93bd
spl set id: 41dc03fc-169b-4691-bd62-9a41d7a6d2f7

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.