Ringworm Control

Manufacturer
Forces of Nature
Effective date
2020-04-28
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:13:04

Label at a glance#

ProductRingworm Control
Active ingredientThuja Occidentalis Leaf, Silicon Dioxide, Sodium Chloride
Label structure8 sections

Dosage and administration

Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area and rub gently into the skin 3 times daily or as directed by a doctor. Supervise children in the use of this product. If condition persists longer than 4 weeks, consult a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

Active IngredientsPurpose
Thuja Occidentalis* 10xRemedy for Ringworm
Silica * 10XRemedy for itchy skin
Natrum Muriaticum* 10xRingworm Remedy

* Certified Organic

Also Contains

INACTIVE INGREDIENT SECTION

South African Pelargonium Graveolens Oil*, Indonesian Eugenia Caryophyllata Oil*, American Sesamum Indicum Oil*, Australian Melaleuca Alternifolia Oil*, Thymus Vulgaris*

Indications

INDICATIONS & USAGE SECTION

For the treatment of ringworm (tinea corporis).

Directions

DOSAGE & ADMINISTRATION SECTION

Clean the affected area and dry thoroughly. Apply a thin layer of the product over affected area and rub gently into the skin 3 times daily or as directed by a doctor. Supervise children in the use of this product. If condition persists longer than 4 weeks, consult a doctor.

Warnings

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Avoid contact with the eyes; in the event of contact, flush with water and seek advice from medical personnel.

OTC - STOP USE SECTION

If irritation occurs or if there is no improvement within 4 weeks, discontinue use and consult a doctor.

OTC - WHEN USING 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. Do not use for diaper rash.

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#: 51393-7599-1

GUARANTEED

FORCES OF NATURE®

Ringworm
CONTROL

Safe and Effective
Ringworm Treatment

  • Rejuvenates Damaged Skin
  • Provides Fast Acting Results
  • Penetrates Deep into the Skin

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

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
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FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51393-7599-1Ringworm Control11 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS113
51393-7599-2Ringworm Control33 mL in 1 BOTTLE, DISPENSINGSOLUTION/ DROPS333

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51393-7599RINGWORM CONTROL (THUJA OCCIDENTALIS LEAF, SILICON DIOXIDE, AND SODIUM CHLORIDE) SOLUTION/ DROPS [FORCES OF NATURE]3Legacy NDC, 2 package rows20200429_9186f981-c071-4e91-8d36-b749434f74dc.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Silicon DioxideACTIVE INGREDIENTETJ7Z6XBU41
Sodium ChlorideACTIVE INGREDIENT451W47IQ8X1
Thuja Occidentalis LeafACTIVE INGREDIENT0T0DQN87861
Silicon DioxideACTIVE MOIETYETJ7Z6XBU41
Sodium CationACTIVE MOIETYLYR4M0NH371
Thuja Occidentalis LeafACTIVE MOIETY0T0DQN87861

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
51393-759951393-7599-1, 51393-7599-2

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 · Source PDF

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
202dceee-2418-4c93-86a1-8d9d5bd3196e9186f981-c071-4e91-8d36-b749434f74dc2020-04-28WarningsExact identifier
spl id: 202dceee-2418-4c93-86a1-8d9d5bd3196e
spl set id: 9186f981-c071-4e91-8d36-b749434f74dc

Reported adverse events (FAERS/openFDA)#

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