EELHOE FUNGAL NAIL TREATMENT- allantoin liquid

EELHOE Fungal Nail Treatment by

Drug Labeling and Warnings

EELHOE Fungal Nail Treatment by is a Otc medication manufactured, distributed, or labeled by Guangdong Ximonth Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL、ALLANTOIN、TOCOPHEROL、ALOE VERA LEAF EXTRACT

Purpose

Repair Nail

Warnings

Please keep out of reach of children.Do not swallow.Please clean your hands before use to ensure the best results from the product.Discontinue use if signs of irritation or rash occur.Store in a cool and dry place.

Use

1.Clean and drythe affected toes and fingers thoroughly.
2.Gently file thick-ened part of the fungal nail with a nail file until it's flat or becomes thinner.
3.Apply a thin layer of liquid using the nail brush onto the affected area.
4.Repeat this process twice a day for 1-2 weeks or until the infection is gone.

STORAGE AND HANDLING

Avoid freezing and excessive heat above 40C (104F) ）
Store in a cool and dry place.

Do not use

Discontinue use if signs of irritation or rash occur.

STOP USE

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

INACTIVE INGREDIENT

AQUA

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EELHOE FUNGAL NAIL TREATMENT 
allantoin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-037
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G)	TEA TREE OIL	7.5 mg  in 30 mg
ALLANTOIN (UNII: 344S277G0Z) (ALLANTOIN - UNII:344S277G0Z)	ALLANTOIN	6 mg  in 30 mg
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	3 mg  in 30 mg
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	4.5 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	9 mL  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-037-01	30 mg in 1 BOX; Type 0: Not a Combination Product	09/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/27/2024

Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)

Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ximonth Technology Co., Ltd.		699436264	manufacture(84660-037)