XIMONTH LIQUID WART CORN CALLUS REMOVER- glycerin liquid

XIMONTH Liquid Wart Corn Callus Remover by

Drug Labeling and Warnings

XIMONTH Liquid Wart Corn Callus Remover 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

GINGER、MELALEUCA ALTERNIFOLIA LEAF

WHEN USING

Clean and dry the skin, apply appropriate amount of this product evenly on the affected skin with warts, corns and calluses, and gently massage until absorbed.

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.

PURPOSE

Removes plantar warts, common warts, corns and calluses on the feet, toes or fingers; reduces inflammation and fights bacteria; soothes skin discomfort; speeds up skin recovery; keeps skin healthy

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

Store in a cool and dry place.

INACTIVE INGREDIENT

WATER、GLYCERIN、ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH LIQUID WART CORN CALLUS REMOVER 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84989-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (MELALEUCA ALTERNIFOLIA LEAF - UNII:G43C57162K)	MELALEUCA ALTERNIFOLIA LEAF	0.006 mg  in 30 mg
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	0.006 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)	27.582 mg  in 30 mg
ALLANTOIN (UNII: 344S277G0Z)	0.006 mg  in 30 mg
GLYCERIN (UNII: PDC6A3C0OX)	2.4 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84989-007-01	30 mg in 1 BOTTLE; Type 0: Not a Combination Product	07/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	07/17/2025

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

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

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ximonth Biotechnology Co., Ltd.		457811606	manufacture(84989-007)