Naturasil Tinea Versicolor Relief

SULFUR TOPICAL HUMAN OTC DRUG

Naturasil Tinea Versicolor Relief is an FDA drug label for the active ingredient SULFUR manufactured by Nature's Innovation, Inc. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260819.

Generic name
SULFUR
Manufacturer
Nature's Innovation, Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
10893-241
Application
N/A
Label effective
20260819

About this product

Naturasil Tinea Versicolor Relief is an FDA-registered drug product whose active ingredient is SULFUR. It is labelled by Nature's Innovation, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 10893-241, label effective 20260819. It is one of 37 FDA drug label records sharing the active ingredient SULFUR. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing SULFUR are most often described in connection with: topical relief, common tinea-prone. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients: Sulfur 6X HPUS The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

Indications & Usage

Uses: Topical Relief for Common Tinea-Prone Areas.

Dosage & Administration

Directions: Shake well. Clean and dry affected area. Apply a thin layer 2-3 times daily. Natural skin tone may take time to return. Moderate sun exposure is essential to help support re-pigmentation. Skin test before first use. Discontinue if irritation occurs.

Warnings

Warnings: For external use only. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. Keep out of reach of children. Do not use if tamper evident seal is broken. In case of ingestion, call Poison Control Center hotline immediately at 1-800-222-1222.

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How products containing SULFUR compare

FDA lists 37 drug label records with SULFUR as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — Boiron 12
— — Nature's Innovation, Inc. 5
— — J. Strickland & Co. 4
— — L'Oreal USA Products Inc 2
— — 111MedCo LLC 1

Frequently asked questions

What is Naturasil Tinea Versicolor Relief used for?
Uses: Topical Relief for Common Tinea-Prone Areas.

Who makes Naturasil Tinea Versicolor Relief?
Nature's Innovation, Inc. is the labeler of record for Naturasil Tinea Versicolor Relief. 37 FDA label records share the active ingredient SULFUR, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Naturasil Tinea Versicolor Relief come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Naturasil Tinea Versicolor Relief prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing SULFUR?
Yes. 37 FDA drug label records list SULFUR as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Naturasil Tinea Versicolor Relief been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.