FDA Label for Ezbiort Toenail Fungus Treatment Pen
View Indications, Usage & Precautions
Ezbiort Toenail Fungus Treatment Pen Product Label
The following document was submitted to the FDA by the labeler of this product Shenzhen Joyuflsh Technology Co.,ltd.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Otc - Active Ingredient
Tolnaftate 1%
UNDECYLENIC ACID 25%
Otc - Purpose
Anti-fungal and Nail Renewal
Indications & Usage
For the effective treatment of nail fungus-including discoloration, thickening, spliting, crumbling, and britleness
Warnings
For external use only.
Otc - Do Not Use
Children under 2 years of age.
Pregnant or if there is any allergic reaction to this produce.
Otc - When Using
Avoid contact with eyes. lf in eyes, rinse thoroughly with water.
Otc - Stop Use
lrritation occurs or discomfort persists
Otc - Keep Out Of Reach Of Children
lf accidental ingestion occurs, seek medical attention immediately and contact a Poison Control Center.
Dosage & Administration
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 Ingredient
ALCOHOL
POLYETHYLENE GLYCOL
PROPYLENE GLYCOL
DIMETHICONE
C12-15 ALKYL LACTATE
ETHYLHEXYLGLYCERIN
GLYCERIN
LAUROCAPRAM
SOPHORA FLAVESCENS ROOT
TOCOPHEROL
PHENOXYETHANOL
WATER
Package Label.Principal Display Panel
* Please review the disclaimer below.
