Gout Control

Manufacturer
Forces of Nature
Effective date
2012-01-03
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:03:30

Label at a glance#

ProductGout Control
Active ingredientArnica Montana, Urtica Urens, Silicon Dioxide, Thuja Occidentalis Root
Label structure8 sections

Dosage and administration

Apply to affected area by gently rubbing into the skin up to 3 or 4 times daily. For children under 2 years of age, consult a doctor before use.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
Arnica Montana* 30CRelieves Pain Associated with Gout
Urtica Urens* 30CRemedy for Acute Pain Associated with Gout
Silica* 8XRelieves Sorenes and Sweling
Thuja Occidentalis* 12XRelieves Burning Pain

* Certified Organic

Also Contains

INACTIVE INGREDIENT SECTION

French Pinus Sylvestris Oil2, French Lavandula Super Oil2, Napalese Matricaria Recutita Oil2, Sesame Oil2

2 Certified Organic

Indications

INDICATIONS & USAGE SECTION

Topical Analgesic: For the temporary relief of gout and minor aches and pains of muscles and joints associated with arthritis.

Directions

DOSAGE & ADMINISTRATION SECTION

Apply to affected area by gently rubbing into the skin up to 3 or 4 times daily. For children under 2 years of age, consult a doctor before use.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with the eyes; if contact occurs, flush with water and seek advice from medical personnel.

OTC - ASK DOCTOR SECTION

If condition worsens or does not improve after regular use of product as directed, consult a doctor. Do not apply to wounds or damaged skin, use for prolonged periods, or use over raw surfaces or blistered areas without consulting a doctor.

SPL UNCLASSIFIED SECTION

Some individuals may be sensitive to tea tree or other oils.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If you are pregnant or breast-feeding, ask a health professional before use.

OTC - DO NOT USE SECTION

Not to be used with children under 2 years of age without physician direction.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep all medicines out of the reach of children.

SPL UNCLASSIFIED SECTION

Manufactured & Distributed by:

Forces of Nature, Inc.
21787 8th Street East #3A
Sonoma, CA 95476 USA

PRINCIPAL DISPLAY PANEL - 11 ml Bottle Carton

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC#: 51393-7655-1

GUARANTEED

FORCES OF NATURE®

Gout
CONTROL

All Natural Gout Remedy

  • Relieves Pain from Gout
  • Treats and Heals
  • Fast Acting

HOMEOPATHIC
MEDICINE

FDA REGISTERED
+
USDA
ORGANIC

Homeopathic Medicine • Certified Organic

11 ml

Principal Display Panel - 11 ml Bottle Carton
Principal Display Panel - 11 ml Bottle Carton

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51393-7655-12019-11-13C16284748780-197449f38-bd56-f6ea-e053-dbdaa90aa703FORCES OF NATURE ® Gout CONTROL
51393-7655-22019-11-13C16284748780-197449f38-bd56-f6ea-e053-dbdaa90aa703FORCES OF NATURE ® Gout CONTROL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-7655-1Gout Control11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS112
51393-7655-2Gout Control33 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS332

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51393-7655GOUT CONTROL (ARNICA MONTANA, URTICA URENS, SILICON DIOXIDE, AND THUJA OCCIDENTALIS ROOT) SOLUTION/ DROPS [FORCES OF NATURE]2Legacy NDC, 2 package rows20120105_8f714935-227d-4aa9-a549-66fc07a26e55.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Arnica MontanaACTIVE INGREDIENTO80TY208ZW2
Silicon DioxideACTIVE INGREDIENTETJ7Z6XBU42
Thuja Occidentalis RootACTIVE INGREDIENT12958C0BR32
Urtica UrensACTIVE INGREDIENTIHN2NQ5OF92
Arnica MontanaACTIVE MOIETYO80TY208ZW2
Silicon DioxideACTIVE MOIETYETJ7Z6XBU42
Thuja Occidentalis RootACTIVE MOIETY12958C0BR32
Urtica UrensACTIVE MOIETYIHN2NQ5OF92
Lavandin OilINACTIVE INGREDIENT9RES347CKG2
Matricaria Chamomilla Flowering Top OilINACTIVE INGREDIENTSA8AR2W4ER2
Pine Needle Oil (Pinus Sylvestris)INACTIVE INGREDIENT5EXL5H740Y2
Sesame OilINACTIVE INGREDIENTQX10HYY4QV2

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51393-765551393-7655-1, 51393-7655-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 3 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
Pine Needle Oil (Pinus Sylvestris)PINE NEEDLE OIL (PINUS SYLVESTRIS)5EXL5H740YLOTION / TOPICAL0.25 %w/wExact identifier — unii candidate
Sesame OilSESAME OILQX10HYY4QVINJECTION / INTRAMUSCULAR70 %v/vExact identifier — unii candidate
2 equally ranked IID candidates
Sesame OilSESAME OILQX10HYY4QVCAPSULE / ORAL2325 mgExact identifier — unii candidate
2 equally ranked IID candidates

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
79027444-53c9-4c61-96f1-c2a38e5215658f714935-227d-4aa9-a549-66fc07a26e552012-01-03WarningsExact identifier
spl id: 79027444-53c9-4c61-96f1-c2a38e521565
spl set id: 8f714935-227d-4aa9-a549-66fc07a26e55

Reported adverse events (FAERS/openFDA)#

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