7 DAYS NAIL FUNGUS TREATMENT- sodium sulfide liquid

7 Days Nail Fungus Treatment by

Drug Labeling and Warnings

7 Days Nail Fungus 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)

Purpose

Restores damage nail & cuticle

Use

1.File the area affected by the nail to enhance the permeability of the essence.2.Clean the surface with a dry swab /cloth.3.Apply the essence to the entire surface of the infected nail.4.Apply the cream twice a day (morning and evening) for at least 4 weeks.

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.

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.

STORAGE AND HANDLING

Avoid freezing and excessive heat above 40C (104F) ）

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

7 DAYS NAIL FUNGUS TREATMENT 
sodium sulfide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-004
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SUNFLOWER OIL (UNII: 3W1JG795YI) (SUNFLOWER OIL - UNII:3W1JG795YI)	SUNFLOWER OIL	3 mg  in 30 mg
SODIUM SULFIDE (UNII: YGR27ZW0Y7) (SULFIDE ION - UNII:G15I91XETI)	SODIUM SULFIDE	7.5 mg  in 30 mg
HYDROGENATED JOJOBA OIL (UNII: 7F674YQ5SO) (HYDROGENATED JOJOBA OIL - UNII:7F674YQ5SO)	HYDROGENATED JOJOBA OIL	6 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	4.5 mg  in 30 mg
WATER (UNII: 059QF0KO0R)	9 mL  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-004-01	30 mg in 1 BOX; Type 0: Not a Combination Product	08/28/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/28/2024

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(84660-004)