FDA Label for Fungal Nail Treatment
View Indications, Usage & Precautions
Fungal Nail Treatment Product Label
The following document was submitted to the FDA by the labeler of this product Guangzhou Yixin Cross-border E-commerce 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.
Active Ingredients
Eucalyptus Globulus Whole 1%
Purpose
Anti-funga
Uses
For the effective treatment of nail fungus, discoloration, thickening, splitting, crumbling and brittleness
Warnings
For external use only.
Dosage And Administration
For initial use, soak the affected nail in warm water to soften it. Gently fle thenail to make it thinner and remove dirt, being cautiousnot to harm the nail bed.
Apply full layers of nail solution with brush onto affected areas on, around, and under nails. A light tingle or burn is normal for the first 10 minutes until the product is absorbed into the skin.
Apply the product twice a day, in the morning and at night.
Visible results will be seen in as little as 7 days, continue regular usage to prevent fungus regrowth.
Do Not Use
Children under 2 years of age
pregnant or if there is any allergic reaction to this produce
When Using Section
Avoid contact with eyes
Stop Use
lrritation occurs or discomfort persists
Keep Out Of Reach Of Children.
lf product gets into eyes, flush with water for 15 minutes.
lf swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredients
Peppermint oil, SAFFLOWER OIL, NOTOGINSENG RADIX
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