Naturasil

Manufacturer: Nature's Innovation, Inc.
Effective date: 2021-01-14
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-01 22:56:34

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.

Contacts and useful links#

PhonePoison Help1-800-222-1222

PhoneLabel contact866.371.2499

Websitewww.naturasil.com

www.naturasil.com

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

Animal Testing

OTHER SAFETY INFORMATION

Not tested on animals.

OTC - PURPOSE SECTION

Purpose

Fungus Growth Relief

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100% Natural Plant Extracts

Naturasil

ml (fl.oz.)

Topical Liquid

Homeopathic Medicine

Athletes Foot

15 mL Label

30 mL Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
SULFUR	ACTIVE INGREDIENT	70FD1KFU70	1
SULFUR	ACTIVE MOIETY	70FD1KFU70	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	1
JOJOBA OIL	INACTIVE INGREDIENT	724GKU717M	1
LAVENDER OIL	INACTIVE INGREDIENT	ZBP1YXW0H8	1
PATCHOULI OIL	INACTIVE INGREDIENT	F3IN55X5PO	1
TEA TREE OIL	INACTIVE INGREDIENT	VIF565UC2G	1
WEST INDIAN LEMONGRASS OIL	INACTIVE INGREDIENT	5BIA40E9ED	1

Products#

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

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

Naturasil Athletes Foot
Sulfur
WEST INDIAN LEMONGRASS OIL
EUCALYPTUS OIL
JOJOBA OIL
LAVENDER OIL
TEA TREE OIL
PATCHOULI OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
10893-260	10893-260-15, 10893-260-30

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
Name	UNII	Kind
SULFUR	70FD1KFU70	ACTIB
WEST INDIAN LEMONGRASS OIL	5BIA40E9ED	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
JOJOBA OIL	724GKU717M	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
TEA TREE OIL	VIF565UC2G	IACT
PATCHOULI OIL	F3IN55X5PO	IACT

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 ingredient	IID ingredient	UNII	Dosage form / route	Potency	Match
EUCALYPTUS OIL	EUCALYPTUS OIL	2R04ONI662	SYRUP / ORAL	NA	Exact identifier — unii candidate
LAVENDER OIL	LAVENDER OIL	ZBP1YXW0H8	GEL / TOPICAL	0.1 %w/w	Exact identifier — unii candidate 2 equally ranked IID candidates
LAVENDER OIL	LAVENDER OIL	ZBP1YXW0H8	INHALANT / NASAL	NA	Exact 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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
db17acae-592a-44a7-863e-2ff341ec724b			cacb2f70-0e5b-427a-bacb-cd40c9e7ffa2	2024-07-26	Warnings	Exact identifier spl set id: cacb2f70-0e5b-427a-bacb-cd40c9e7ffa2

Reported adverse events (FAERS/openFDA)#

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