FDA.reportPublic FDA data

Gout-Gone

Manufacturer
Feelgood Health | W. Last
Effective date
2011-07-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:03:15

Label at a glance#

ProductGout-Gone
Active ingredientANTIMONY TRISULFIDE, CANDIDA PARAPSILOSIS, LEDUM PALUSTRE TWIG, 2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATE, SILICON DIOXIDE, STRYCHNOS NUX-VOMICA SEED
Label structure11 sections

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Relieves swelling, inflammation and burning joint pain

INDICATIONS & USAGE SECTION

Indications:  Homeopathic remedy for the relief of acute swelling, inflammation and burning pain in small joints, especially the big toe.

DOSAGE & ADMINISTRATION SECTION

Dosage: Mix 10 drops in ¼ cup water and sip slowly. Repeat every 20-30 minutes as needed until symptoms subside. If preferred, drops may be taken directly into the mouth.

GENERAL PRECAUTIONS SECTION

Caution: Consult your doctor if symptoms persist or worsen. If pregnant or breastfeeding, ask a health professional before use. Keep this and all medicines out of reach of children.

OTC - ACTIVE INGREDIENT SECTION

Ingredients: Each dose contains equal parts of Antimonium crud (6C) (HPUS), Quercus (12C) (HPUS), Rhododendron (6C) (HPUS), Benzoic ac (6C) (HPUS), Silicea (6X) (HPUS), Nux vom (6C) (HPUS), Ledum (6C) (HPUS)

INACTIVE INGREDIENT SECTION

Citricidal Extract (inactive ingredient)

PREGNANCY SECTION

If pregnant or breastfeeding, ask a health professional before use.

WARNINGS SECTION

Contains no animal products, gluten, artificial flavors, preservatives, colorants or alcohol. Suitable for vegetarians and safe for all ages.

INFORMATION FOR PATIENTS SECTION

All Native Remedies health products are especially formulated by experts in the field of natural health and are manufactured according to the highest pharmaceutical standards for maximum safety and effectiveness. For more information, visit us at www.nativeremedies.com

Distributed by

Native Remedies, LLC

6531 Park of Commerce Blvd.

Suite 160

Boca Raton, FL 33487

Phone: 1.877.289.1235

International: + 1.561.999.8857

The letters HPUS indicate that the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopoeia of the United States.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

bottle labelbottle label

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep this and all medications out of reach of children.

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130810845017206GTIN-13: 0810845017206
EAN-13: 0810845017206
GTIN-12: 810845017206
UPC-A: 810845017206
GTIN storage (14 digits): 00810845017206		GoutGone.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68647-168-102019-10-29C16284748780-1960f7f55-da6c-8e05-e053-dbdaa90a074aGOUT-GONE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68647-168-10Gout-Gone50000 mL in 1 BOTTLE, GLASSTINCTURE500003

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68647-168GOUT-GONE (ANTIMONIUM CRUD , QUERCUS , RHODODENDRON, BENZOIC AC , SILICEA , NUX VOM , LEDUM , CITRICIDAL EXTRACT ) TINCTURE [FEELGOOD HEALTH]3Legacy NDC, 1 package rows20110708_219db8a4-c79e-4381-8d9c-8020b2b3491c.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATEACTIVE INGREDIENT93NOD9WBCS3
ANTIMONY TRISULFIDEACTIVE INGREDIENTF79059A38U3
CANDIDA PARAPSILOSISACTIVE INGREDIENT0KZ676D44N3
LEDUM PALUSTRE TWIGACTIVE INGREDIENT877L01IZ0P3
SILICON DIOXIDEACTIVE INGREDIENTETJ7Z6XBU43
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH139193
2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATEACTIVE MOIETY93NOD9WBCS3
ANTIMONY CATION (3+)ACTIVE MOIETY069647RPT53
CANDIDA PARAPSILOSISACTIVE MOIETY0KZ676D44N3
LEDUM PALUSTRE TWIGACTIVE MOIETY877L01IZ0P3
SILICON DIOXIDEACTIVE MOIETYETJ7Z6XBU43
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH139193
CITRUS PARADISI SEEDINACTIVE INGREDIENT12F08874Y73
WATERINACTIVE INGREDIENT059QF0KO0R3

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
68647-16868647-168-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ANTIMONY TRISULFIDEF79059A38UACTIB
CANDIDA PARAPSILOSIS0KZ676D44NACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
2-ETHYLHEXYL 4-PHENYLBENZOPHENONE-2'-CARBOXYLATE93NOD9WBCSACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
LEDUM PALUSTRE TWIG877L01IZ0PACTIB
CITRUS PARADISI SEED12F08874Y7IACT
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
160ecf24-1f35-4a71-a5ad-8d3c4b0cb880219db8a4-c79e-4381-8d9c-8020b2b3491c2011-07-08WarningsExact identifier
spl id: 160ecf24-1f35-4a71-a5ad-8d3c4b0cb880
spl set id: 219db8a4-c79e-4381-8d9c-8020b2b3491c

Reported adverse events (FAERS/openFDA)#

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