Naturasil Scabies

Naturasil Scabies 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 20210114.

Generic: SULFUR

Manufacturer: Nature's Innovation, Inc.

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 10893-420

Application:

Effective: 20210114

Active Ingredients: Drug Facts Active Ingredients: Sulfur 1X 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 treatment of scabies

Dosage & Administration

Directions: Cleanse skin thoroughly before applying. Cover the affected area with cream one time per day. If excessive drying of the skin or rash occurs, reduce the application of product or discontinue use. To speed relief, we recommend to use Naturasil Sulfur Lavender Soap. Some individuals may be senstive to sulfur or essential oils. Skin test for tolerability. If irritation or reaction occurs, discontinue use.

Contraindications

Not available.

Warnings

Warnings: For external use only. Ask a doctor before use if pregnant or nursing. Avoid using near eyes, mouth or mucous membranes. If eye contact occurs, rinse thoroughly with water and consult a doctor. 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.

Adverse Reactions

Not available.

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