FDA.reportPublic FDA data

Naturasil

Manufacturer
Nature's Innovation, Inc.
Effective date
2011-10-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:50:31

Label at a glance#

ProductNaturasil Athletes Foot
Active ingredientSULFUR
Label structure9 sections

Indications and uses

Uses : Symptomatic treatment of athletes foot ( tinea pedis ).

Dosage and administration

Directions: Thoroughly wash and dry affected area. Apply a few drops of product 2-3 times per day to the affected area for 4-7 days or until infection has subsided. To speed healing, we recommend Naturasil Sulfur-Lavender Multi-Purpose Medicated soap. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Drug Facts

Active Ingredients:                
Sulfur 6X HPUS                           

DESCRIPTION SECTION

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

Uses

INDICATIONS & USAGE SECTION

Uses: Symptomatic treatment of athletes foot (tinea pedis).

Warnings

WARNINGS SECTION

Warnings: For external use only.

OTC - ASK DOCTOR SECTION

Ask a doctor before use if pregnant or nursing.

OTHER SAFETY INFORMATION

Avoid using near eyes, mouth or mucous membranes.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OTC - DO NOT USE SECTION

Do not use if tamper evident seal is broken.

OTHER SAFETY INFORMATION

In case of ingestion call Poison Control Center hotline immediately at 1-800-222-1222.

Directions

DOSAGE & ADMINISTRATION SECTION

Directions:Thoroughly wash and dry affected area. Apply a few drops of product 2-3 times per day to the affected area for 4-7 days or until infection has subsided. To speed healing, we recommend Naturasil Sulfur-Lavender Multi-Purpose Medicated soap. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Cymbopogon Citratus Leaf Oil, Eucalyptus Leaf Oil, Jojoba Seed Oil, Lavender Oil, Melaleuca Alternifolia Leaf Oil, Patchouli Leaf Oil.

Questions

OTC - QUESTIONS SECTION

Questions? Comments? www.naturasil.com 866.371.2499 Mfd. by:
Nature's Innovation, Inc. 2723 Brickton North Dr., Buford, GA 30518

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100% Natural Plant Extracts

Naturasil

30 ml (1.014 fl.oz.)

Topical Liquid

Homeopathic Medicine

Athletes Foot

Image Athletes Foot 30 mlImage Athletes Foot 30 ml

Animal Testing

OTHER SAFETY INFORMATION

Not tested on animals.

OTC - PURPOSE SECTION

Purpose

Fungus Growth Relief

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10893-625-302020-02-04C16284748780-19d75b9d0-3ed4-f424-e053-dadaa90a57ceAthlete's Foot 30ml Labeling
10893-625-302020-01-31C16284748780-19d75b9d0-3ed4-f424-e053-dadaa90a57ceAthlete's Foot 30ml Labeling

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU702
SULFURACTIVE MOIETY70FD1KFU702
EUCALYPTUS OILINACTIVE INGREDIENT2R04ONI6622
JOJOBA OILINACTIVE INGREDIENT724GKU717M2
LAVENDER OILINACTIVE INGREDIENTZBP1YXW0H82
PATCHOULI OILINACTIVE INGREDIENTF3IN55X5PO2
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G2
WEST INDIAN LEMONGRASS OILINACTIVE INGREDIENT5BIA40E9ED2

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10893-62510893-625-30

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70ACTIB
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
EUCALYPTUS OIL2R04ONI662IACT
JOJOBA OIL724GKU717MIACT
LAVENDER OILZBP1YXW0H8IACT
TEA TREE OILVIF565UC2GIACT
PATCHOULI OILF3IN55X5POIACT

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
LAVENDER OILLAVENDER OILZBP1YXW0H8INHALANT / NASALNAExact identifier — unii candidate
2 equally ranked IID candidates
EUCALYPTUS OILEUCALYPTUS OIL2R04ONI662SYRUP / ORALNAExact identifier — unii candidate
LAVENDER OILLAVENDER OILZBP1YXW0H8GEL / TOPICAL0.1 %w/wExact 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
46881a1a-2197-49e6-a5d5-fbb6fffe88e62e996837-9c63-48e1-a4b7-d6e1d895f5922011-10-01WarningsExact identifier
spl id: 46881a1a-2197-49e6-a5d5-fbb6fffe88e6
spl set id: 2e996837-9c63-48e1-a4b7-d6e1d895f592

Reported adverse events (FAERS/openFDA)#

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