EZBIORT Toenail Fungus Treatment Pen
83766-107 EZBIORT Toenail Fungus Treatment Pen
3dcdb0c4-e0ec-dfee-e063-6294a90a0bda
HUMAN OTC DRUG LABEL
Sep 2, 2025
Shenzhen Joyuflsh Technology Co.,Ltd.
DUNS: 603012375
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Tolnaftate, UNDECYLENIC ACID
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
Product Classification
Product Specifications
INGREDIENTS (14)
Drug Labeling Information
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
INDICATIONS & USAGE SECTION
For the effective treatment of nail fungus-including discoloration, thickening, spliting, crumbling, and britleness
OTC - ACTIVE INGREDIENT SECTION
Tolnaftate 1%
UNDECYLENIC ACID 25%
OTC - PURPOSE SECTION
Anti-fungal and Nail Renewal
WARNINGS SECTION
For external use only.
OTC - DO NOT USE SECTION
Children under 2 years of age.
Pregnant or if there is any allergic reaction to this produce.
DOSAGE & ADMINISTRATION SECTION
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.
OTC - WHEN USING SECTION
Avoid contact with eyes. lf in eyes, rinse thoroughly with water.
OTC - STOP USE SECTION
lrritation occurs or discomfort persists
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
lf accidental ingestion occurs, seek medical attention immediately and contact a Poison Control Center.
INACTIVE INGREDIENT SECTION
ALCOHOL
POLYETHYLENE GLYCOL
PROPYLENE GLYCOL
DIMETHICONE
C12-15 ALKYL LACTATE
ETHYLHEXYLGLYCERIN
GLYCERIN
LAUROCAPRAM
SOPHORA FLAVESCENS ROOT
TOCOPHEROL
PHENOXYETHANOL
WATER