DRAWZONE Toenail Fungus Treatment Pen

Tolnaftate, UNDECYLENIC ACID · Liquid · Topical

Over the counter

Active ingredient

Tolnaftate 1% UNDECYLENIC ACID 25%

Purpose

Anti-fungal and Nail Renewal

Uses

For the effective treatment of nail fungus-including discoloration, thickening, spliting, crumbling, and britleness

Warnings

For external use only.

Do not use

Children under 2 years of age. Pregnant or if there is any allergic reaction to this produce.

When using this product

Avoid contact with eyes. lf in eyes, rinse thoroughly with water.

Stop use and ask a doctor

lrritation occurs or discomfort persists

Keep out of reach of children

lf accidental ingestion occurs, seek medical attention immediately and contact a Poison Control Center.

Directions

1.Wash and dry your nails thoroughly before applying the product. Remove the cap that covers the brush. 2.Twist the end of the pen clockwise to dispense the liquid onto the brush. 3.Apply the liquid three times to the areas requiring treatment, ensuring complete coverage of all affected parts. 4.Use 2 times daily for 2-4 weeks, depending on the condition being treated.

Inactive ingredients

ALCOHOL POLYETHYLENE GLYCOL PROPYLENE GLYCOL DIMETHICONE C12-15 ALKYL LACTATE ETHYLHEXYLGLYCERIN GLYCERIN LAUROCAPRAM SOPHORA FLAVESCENS ROOT TOCOPHEROL PHENOXYETHANOL WATER

Label text from the FDA structured product label by Shenzhen Joyuflsh Technology Co.,Ltd. (revised Sep 5, 2025). Long sections are shortened; the complete label is on DailyMed.

Active ingredients

DRAWZONE Toenail Fungus Treatment Pen NDC products (1)

NDCStrength & formLabelerType
83766-107Undecylenic Acid 25 g/100mL; Tolnaftate 1 g/100mL
Liquid
Shenzhen Joyuflsh Technology Co.,Ltd.OTC MONOGRAPH DRUG

Frequently asked questions

What is DRAWZONE Toenail Fungus Treatment Pen used for?

For the effective treatment of nail fungus-including discoloration, thickening, spliting, crumbling, and britleness

Who makes DRAWZONE Toenail Fungus Treatment Pen?

DRAWZONE Toenail Fungus Treatment Pen is listed by 1 labeler in the FDA NDC directory, including Shenzhen Joyuflsh Technology Co.,Ltd..