Gout Symptom Formula

Manufacturer
King Bio Inc.
Effective date
2024-11-20
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:29:00

Label at a glance#

ProductGout Symptom Formula
Active ingredientAMMONIUM PHOSPHATE, DIBASIC, ATROPA BELLADONNA, COLCHICUM AUTUMNALE BULB, FORMIC ACID, FRAXINUS EXCELSIOR LEAF, RHODODENDRON TOMENTOSUM LEAFY TWIG, SODIUM CARBONATE, STRYCHNOS NUX-VOMICA SEED, URTICA URENS WHOLE
Label structure9 sections

Indications and uses

For temporary relief of symptoms in toes, heels, feet, or joints:  discomforts  cramping  tender or itchy joints As per various homeopathic materia medicas. Claims based on traditional homeopathic practice, not accepted medical evidence. These uses have not been evaluated by the FDA, and product has not been clinically tested. Reference image: Gout.jpg

Dosage and administration

Initially, depress pump until primed. Spray one dose directly into mouth. Adults (18 years of age and up): 3 sprays 3 times per day. Children under 18: Consult a physician. Use additionally as needed, up to 6 times per day. Reference image: Gout.jpg

Label contents#

Full prescribing information#

Directions

DOSAGE & ADMINISTRATION SECTION

Initially, depress pump until
primed.

Spray one dose directly into
mouth.

Adults (18 years of age and up):
3 sprays 3 times per day.

Children under 18: Consult a
physician.

Use additionally as needed, up
to 6 times per day.

Reference image: Gout.jpg

OTHER SAFETY INFORMATION

Other information

Tamper resistant for your protection.

Use only if safety seal is intact.

Keep carton for complete drug facts and product information.

Questions? Call 866.298.2740

King Bio, Inc. 3 Westside Drive

Asheville, NC 2806 USA

FDA Reg. #1053442

For latest product information and instructions: www.DrKings.com

Reference image: Gout.jpg

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Citrus Extract (ascorbic acid, citric acid, citrus aurantium amara fruit extract, citrus aurantium sinensis peel extract, citrus reticulata fruit extact, demineralized water, glycerin, lactic acid), Honeysuckle (Lonicera japonica), Polylysine, Purified Water, Shagbark Hickory (Carya Ovata) Bark Extract, Steviol (Steviol Glycosides).

Reference image: Gout.jpg

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Equal volumes of each HPUS ingredient in 10X, 30X, and 1LM
potencies.

Ammonium phosphoricum, Belladonna, Colchicum autumnale, Formicum acidum, Fraxinus excelsior, Ledum palustre, Natrum carbonicum,
Nux vomica, Urtica urens.

HPUS” indicates the active ingredients are in the official
Homeopathic Pharmacopeia of the United States.

Reference image: Gout.jpg

Uses

INDICATIONS & USAGE SECTION

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

discomforts 

cramping 

tender or itchy joints

As per various homeopathic materia medicas. Claims based
on traditional homeopathic practice, not accepted medical
evidence. These uses have not been evaluated by the FDA,
and product has not been clinically tested.

Reference image: Gout.jpg

Warnings

WARNINGS SECTION

Stop use and consult a physician 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.

In case of overdose, get medical help or contact a Poison Control Center immediately.

Reference image: Gout.jpg

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.

Reference image: Gout.jpg

OTC - PURPOSE SECTION

Equal volumes of each HPUS ingredient in 10X, 30X, and 1LM
potencies.

Ammonium phosphoricum......................... 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

HPUS” indicates the active ingredients are in the official
Homeopathic Pharmacopeia of the United States.

Reference image: Gout.jpg

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image description Gout.jpgimage description Gout.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
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
57955-2826GOUT SYMPTOM FORMULA (AMMONIUM PHOSPHORICUM, BELLADONNA, COLCHICUM AUTUMNALE, FORMICUM ACIDUM, FRAXINUS EXCELSIOR, LEDUM PALUSTRE, NATRUM CARBONICUM, NUX VOMICA, URTICA URENS.) LIQUID [KING BIO INC.]2Legacy NDC20241122_b033adc0-1290-4ecf-8e9b-50193ca0c37f.zip

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
57955-282657955-2826-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

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
62a0f809-5388-439f-a7c8-fa2546315949b033adc0-1290-4ecf-8e9b-50193ca0c37f2025-11-10WarningsExact identifier
spl set id: b033adc0-1290-4ecf-8e9b-50193ca0c37f

Reported adverse events (FAERS/openFDA)#

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