Sunmark Benzoin Compound Tincture

Sunmark Benzoin Compound Tincture is an FDA drug label for the active ingredient BENZOIN RESIN manufactured by Strategic Sourcing Services 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 20231219.

Generic: BENZOIN RESIN

Manufacturer: Strategic Sourcing Services LLC

Product Type: HUMAN OTC DRUG

Route: TOPICAL

Dosage Form:

NDC: 49348-138

Application: M022

Effective: 20231219

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