XIMONTH FOOT SANITIZER- glycerin liquid

XIMONTH Foot Sanitizer by

Drug Labeling and Warnings

XIMONTH Foot Sanitizer by is a Otc medication manufactured, distributed, or labeled by Shantou Ximonth Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

CAMELLIA SINENSIS SEED OIL、ALOE BARBADENSIS EXTRACT

PURPOSE

1. Contains tea tree oil, which can eradicate fungi and relieve foot fungal problems.

2. Use in multiple scenarios, can be used on feet, socks and shoes.

3. It can strengthen and protect the skin for a long time and prevent reinfection.

4. It uses mild ingredients and will not cause damage to the skin.

WHEN USING

1. Completely clean and dry foot skin

2. Take an appropriate amount of this product and spray it on your feet, shoes or socks

3. Wait 2-3 minutes for your feet to fully absorb it.

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

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

INACTIVE INGREDIENT

AQUA、GLYCERIN、UREA、COLLOIDAL SILVER

INDICATIONS & USAGE

1. Completely clean and dry foot skin

2. Take an appropriate amount of this product and spray it on your feet, shoes or socks

3. Wait 2-3 minutes for your feet to fully absorb it.

DOSAGE & ADMINISTRATION

1. Completely clean and dry foot skin

2. Take an appropriate amount of this product and spray it on your feet, shoes or socks

3. Wait 2-3 minutes for your feet to fully absorb it.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH FOOT SANITIZER 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84989-019
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMELLIA SINENSIS SEED OIL (UNII: O5R6DK2M9K) (CAMELLIA SINENSIS SEED OIL - UNII:O5R6DK2M9K)	CAMELLIA SINENSIS SEED OIL	0.02 mg  in 100 mg
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) (ALOE BARBADENSIS LEAF - UNII:ZY81Z83H0X)	ALOE BARBADENSIS LEAF	0.02 mg  in 100 mg

Inactive Ingredients
Ingredient Name	Strength
UREA (UNII: 8W8T17847W)	5 mg  in 100 mg
COLLOIDAL SILVER (UNII: 3M4G523W1G)	0.5 mg  in 100 mg
AQUA (UNII: 059QF0KO0R)	90.46 mg  in 100 mg
GLYCERIN (UNII: PDC6A3C0OX)	4 mg  in 100 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84989-019-01	100 mg in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/30/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	03/30/2026

Labeler - Shantou Ximonth Biotechnology Co., Ltd. (457811606)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ximonth Biotechnology Co., Ltd.		457811606	manufacture(84989-019)