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.
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.
Drug Facts
Topical Analgesic: For the temporary relief of gout and minor aches and pains of muscles and joints associated with arthritis.
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.
For external use only.
Avoid contact with the eyes; if contact occurs, flush with water and seek advice from medical personnel.
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.
Some individuals may be sensitive to tea tree or other oils.
If you are pregnant or breast-feeding, ask a health professional before use.
Not to be used with children under 2 years of age without physician direction.
Keep all medicines out of the reach of children.
Manufactured & Distributed by:
Forces of Nature, Inc.
21787 8th Street East #3A
Sonoma, CA 95476 USA
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 51393-7655-1 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bd56-f6ea-e053-dbdaa90aa703 | FORCES OF NATURE ® Gout CONTROL |
| 51393-7655-2 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bd56-f6ea-e053-dbdaa90aa703 | FORCES OF NATURE ® Gout CONTROL |
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51393-7655-1 | Gout Control | 11 mL in 1 BOTTLE, DISPENSING | SOLUTION/ DROPS | 11 | 2 | |
| 51393-7655-2 | Gout Control | 33 mL in 1 BOTTLE, DISPENSING | SOLUTION/ DROPS | 33 | 2 |
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51393-7655 | GOUT CONTROL (ARNICA MONTANA, URTICA URENS, SILICON DIOXIDE, AND THUJA OCCIDENTALIS ROOT) SOLUTION/ DROPS [FORCES OF NATURE] | 2 | Legacy NDC, 2 package rows | 20120105_8f714935-227d-4aa9-a549-66fc07a26e55.zip |
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Arnica Montana | ACTIVE INGREDIENT | O80TY208ZW | 2 | |
| Silicon Dioxide | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 2 | |
| Thuja Occidentalis Root | ACTIVE INGREDIENT | 12958C0BR3 | 2 | |
| Urtica Urens | ACTIVE INGREDIENT | IHN2NQ5OF9 | 2 | |
| Arnica Montana | ACTIVE MOIETY | O80TY208ZW | 2 | |
| Silicon Dioxide | ACTIVE MOIETY | ETJ7Z6XBU4 | 2 | |
| Thuja Occidentalis Root | ACTIVE MOIETY | 12958C0BR3 | 2 | |
| Urtica Urens | ACTIVE MOIETY | IHN2NQ5OF9 | 2 | |
| Lavandin Oil | INACTIVE INGREDIENT | 9RES347CKG | 2 | |
| Matricaria Chamomilla Flowering Top Oil | INACTIVE INGREDIENT | SA8AR2W4ER | 2 | |
| Pine Needle Oil (Pinus Sylvestris) | INACTIVE INGREDIENT | 5EXL5H740Y | 2 | |
| Sesame Oil | INACTIVE INGREDIENT | QX10HYY4QV | 2 |
Every source-derived product name is available through these pages.
| Product NDC | Package NDC |
|---|---|
| 51393-7655 | 51393-7655-1, 51393-7655-2 |
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| Arnica Montana | O80TY208ZW | ACTIB |
| Urtica Urens | IHN2NQ5OF9 | ACTIB |
| Silicon Dioxide | ETJ7Z6XBU4 | ACTIB |
| Thuja Occidentalis Root | 12958C0BR3 | ACTIB |
| Pine Needle Oil (Pinus Sylvestris) | 5EXL5H740Y | IACT |
| Lavandin Oil | 9RES347CKG | IACT |
| Matricaria Chamomilla Flowering Top Oil | SA8AR2W4ER | IACT |
| Sesame Oil | QX10HYY4QV | IACT |
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| Pine Needle Oil (Pinus Sylvestris) | PINE NEEDLE OIL (PINUS SYLVESTRIS) | 5EXL5H740Y | LOTION / TOPICAL | 0.25 %w/w | ||
| Sesame Oil | SESAME OIL | QX10HYY4QV | INJECTION / INTRAMUSCULAR | 70 %v/v | ||
| Sesame Oil | SESAME OIL | QX10HYY4QV | CAPSULE / ORAL | 2325 mg |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 79027444-53c9-4c61-96f1-c2a38e521565 | 8f714935-227d-4aa9-a549-66fc07a26e55 | 2012-01-03 | Warnings | 79027444-53c9-4c61-96f1-c2a38e521565 8f714935-227d-4aa9-a549-66fc07a26e55 |
Adverse event summaries are temporarily unavailable. Other product information remains available.