FUNGAL NAIL TREATMENT liquid

Fungal Nail Treatment by

Drug Labeling and Warnings

Fungal Nail Treatment by is a Otc medication manufactured, distributed, or labeled by Guangzhou Yixin Cross-border E-commerce Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

FUNGAL NAIL TREATMENT 
fungal nail treatment liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84778-075
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
EUCALYPTUS GLOBULUS WHOLE (UNII: SI1P2XF3M3) (EUCALYPTUS GLOBULUS WHOLE - UNII:SI1P2XF3M3)	EUCALYPTUS GLOBULUS WHOLE	1 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
PEPPERMINT OIL (UNII: AV092KU4JH)
PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)
SAFFLOWER OIL (UNII: 65UEH262IS)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84778-075-01	15 g in 1 BOTTLE; Type 0: Not a Combination Product	06/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M029	06/14/2025

Labeler - Guangzhou Yixin Cross-border E-commerce Co., Ltd. (455800881)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Yixin Cross-border E-commerce Co., Ltd.		455800881	manufacture(84778-075) , label(84778-075)