Benzoin Tincture

Benzoin Tincture is an FDA drug label for the active ingredient BENZOIN RESIN manufactured by Pharma Nobis, LLC 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 20231226.

Generic: BENZOIN RESIN

Manufacturer: Pharma Nobis, LLC

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 82645-924

Application: M022

Effective: 20231226

Active Ingredients: Active Ingredient Benzoin

Indications & Usage

Use Forms a coating over wound for protecting recurring canker sores

Dosage & Administration

Directions Adults and children 6 months of age and older: Dry the affected area, with cotton swab, apply undiluted to the affected area not more often than every 2 hours. Children under 6 months of age: Consult a dentiest or doctor.

Contraindications

Not available.

Warnings

Warnings For external use only. Do not swallow. Do not exceed recommended dosage.

Adverse Reactions