Naturasil Scabies Relief

SULFUR, THUJA OCCINDENTALIS TOPICAL HUMAN OTC DRUG

Naturasil Scabies Relief is an FDA drug label for the active ingredient SULFUR, THUJA OCCINDENTALIS manufactured by Natures 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 20201022.

Generic name
SULFUR, THUJA OCCINDENTALIS
Manufacturer
Natures Innovation, Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
10893-640
Application
N/A
Label effective
20201022

About this product

Naturasil Scabies Relief is an FDA-registered drug product whose active ingredient is SULFUR, THUJA OCCINDENTALIS. It is labelled by Natures Innovation, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 10893-640, label effective 20201022. 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, THUJA OCCINDENTALIS are most often described in connection with: symptomatic homeopathic, topical treatment, common parasitic, skin conditions. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredients: Sulfur 1X HPUS, Thuja Occindentalis 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: Symptomatic homeopathic topical treatment of common parasitic skin conditions and scabies.

Dosage & Administration

Directions: Use soap at least 2 times per day, for 4-10 days. Drying of skin may occur. Some individuals may be sensitive to essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Warnings

Warnings: For external use only. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. If contact with eyes or mucous membranes occurs, rinse thoroughly with water. Keep out of reach of children. In case of ingestion, call Poison Control Center hotline immediately at 1-800-222-1222

Frequently asked questions

What is Naturasil Scabies Relief used for?
Uses: Symptomatic homeopathic topical treatment of common parasitic skin conditions and scabies.

Who makes Naturasil Scabies Relief?
Natures Innovation, Inc. is the labeler of record for Naturasil Scabies Relief.

What form does Naturasil Scabies 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 Scabies 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.

Has Naturasil Scabies 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.