FDA.reportPublic FDA data

Naturasil

Manufacturer
Nature's Innovation, Inc.
Effective date
2011-10-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:50:32

Label at a glance#

ProductNaturasil Scabies
Active ingredientSULFUR
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION


DrugFacts

Active Ingredients:

Sulfur 6X HPUS

DESCRIPTION SECTION

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

OTC - PURPOSE SECTION

Purpose

Scabies Symptom Relief

INDICATIONS & USAGE SECTION

Uses: Symptomatic treatment scabies.

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.

DOSAGE & ADMINISTRATION SECTION

Directions:  Add 10-20 drops to bath water. Soak for 20 minutes, air dry. May be used for spot treatment. To speed relief, we recommend to use Naturasil Sulfur Lavender Soap. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

Cymbopogon Citratus Leaf Oil,

Melaleuca Alternifolia Leaf Oil.

OTC - QUESTIONS SECTION

Questions? Comments?

www.naturasil.com 1-866-371-2499

Mfd. by: Nature's Innovation, Inc.,

2723 Brickton North Dr., Buford, GA 30518

Not tested on animals.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

100% Natural Plant Extracts

Naturasil

10ml (.34 fl. oz.)

Topical Liquid

Homeopathic Medicine

Scabies

Image of Scabies Topical Liquid 10 ml
Image of Scabies Topical Liquid 10 ml

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10893-335-102020-02-04C16284748780-19d75b9cf-d994-f424-e053-dadaa90a57ceScabies Topical Liquid 10 ml Label
10893-335-102020-01-31C16284748780-19d75b9cf-d994-f424-e053-dadaa90a57ceScabies Topical Liquid 10 ml Label

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SULFURACTIVE INGREDIENT70FD1KFU701
SULFURACTIVE MOIETY70FD1KFU701
TEA TREE OILINACTIVE INGREDIENTVIF565UC2G1
WEST INDIAN LEMONGRASS OILINACTIVE INGREDIENT5BIA40E9ED1

Products#

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

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10893-33510893-335-10

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Name, UNII, Kind table
NameUNIIKind
SULFUR70FD1KFU70ACTIB
WEST INDIAN LEMONGRASS OIL5BIA40E9EDIACT
TEA TREE OILVIF565UC2GIACT

Source Document#

Source XML

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
740ab809-0ebc-430e-ba4d-c6a1e4c1e5f998aa5772-4e39-428d-a6f4-d8fb7be7ec3d2011-10-01WarningsExact identifier
spl id: 740ab809-0ebc-430e-ba4d-c6a1e4c1e5f9
spl set id: 98aa5772-4e39-428d-a6f4-d8fb7be7ec3d

Reported adverse events (FAERS/openFDA)#

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