Active Ingredients
Eucalyptus Globulus Whole 1%
Fungal Nail Treatment Liquid
FDA Label NDC 84778-075
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Yixin Cross-border E-commerce Co., Ltd. for the product Fungal Nail Treatment (NDC 84778-075). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredients, purpose, uses, warnings, dosage and administration, do not use, when using section, stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
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
Principal Display Panel
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