TOENAIL FUNGUS TREATMENT- terbinafine liquid

Toenail Fungus Treatment by

Drug Labeling and Warnings

Toenail Fungus Treatment by is a Otc medication manufactured, distributed, or labeled by Shenzhen Wankelai E-commerce Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Terbinafine 1%

PURPOSE

Antifungal

INDICATIONS & USAGE

For the effective treatment of nail fungus, discoloration, thickening, splitting,
crumbling and brittleness.

WARNINGS

For external use only.

DO NOT USE

If on children under 2 years of age unless directed by a doctor.

WHEN USING

·Avoid contact with eyes.

STOP USE

Irritation occurs or if there is no improvement within 4 weeks.

KEEP OUT OF REACH OF CHILDREN

If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Apply the product twice a day, in the morning and at night.
Soak nails in warm water to soften, then gently file affected nails.
Clean the affected area with soap and water and dry thoroughly.
Directly to affected nail
Allow a few minutes to dry after each.
Use daily for 4-6 weeks, depending on the condition of the area needing repair.

INACTIVE INGREDIENT

ALCOHOL,DIMETHICONE,CETOSTEARYL ALCOHOL,TEA TREE OIL,PROPYLENE GLYCOL,TOCOPHEROL,SAFFLOWER OIL,WATER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

TOENAIL FUNGUS TREATMENT 
terbinafine liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87413-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TERBINAFINE (UNII: G7RIW8S0XP) (TERBINAFINE - UNII:G7RIW8S0XP)	TERBINAFINE	0.01 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
SAFFLOWER OIL (UNII: 65UEH262IS)
ALCOHOL (UNII: 3K9958V90M)
TOCOPHEROL (UNII: R0ZB2556P8)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
DIMETHICONE 1000 (UNII: MCU2324216)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87413-002-01	10 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/24/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M005	03/24/2026

Labeler - Shenzhen Wankelai E-commerce Co., Ltd. (624221031)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhen Wankelai E-commerce Co., Ltd.		624221031	manufacture(87413-002)