XIMONTH NAIL REPAIRS PATCHES- glycerin patch

XIMONTH Nail Repairs Patches by

Drug Labeling and Warnings

XIMONTH Nail Repairs Patches 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

SOPHORA ANGUSTIFOLIA ROOT EXTRACT、ALOE BARBADENSIS EXTRACT

PURPOSE

1. A variety of moisturizing ingredients are absorbed into nails and skin through the patch, deeply nourishing, hydrating brittle nails, and reducing the appearance of thick and discolored nails.

2. Replenish nails with necessary moisture and nutrients, quickly reduce brittle manicure overnight, and restore manicure to show its natural, healthy appearance.

3. Hygienic material support, soft and strong, can provide gentle repair to nails.

4. The packaging is compact and easy to use. The patch design is suitable for carrying when going out and can be used anytime and anywhere.

WHEN USING

WARNINGS

Keep out of reach of children.Avoid contact with eyes.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

Keep out of reach of children.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA、GLYCERIN、ALLANTOIN

INDICATIONS & USAGE

1. Wash and dry affected nails before going to bed

2. Open the package, take out the patch and tear off the back film

3. Place the patch on the nail and remove it after about 6-8 hours

DOSAGE & ADMINISTRATION

1. Wash and dry affected nails before going to bed

2. Open the package, take out the patch and tear off the back film

3. Place the patch on the nail and remove it after about 6-8 hours

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH NAIL REPAIRS PATCHES 
glycerin patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84989-015
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) (ALOE BARBADENSIS LEAF - UNII:ZY81Z83H0X)	ALOE BARBADENSIS LEAF	0.012 mg  in 60 mg
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K) (SOPHORA FLAVESCENS ROOT - UNII:IYR6K8KQ5K)	SOPHORA FLAVESCENS ROOT	0.012 mg  in 60 mg

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	0.06 mg  in 60 mg
GLYCERIN (UNII: PDC6A3C0OX)	3 mg  in 60 mg
AQUA (UNII: 059QF0KO0R)	56.916 mg  in 60 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84989-015-01	60 mg in 1 BOX; Type 0: Not a Combination Product	01/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	01/09/2026

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

Establishment
Name	Address	ID/FEI	Business Operations
Shantou Ximonth Biotechnology Co., Ltd.		457811606	manufacture(84989-015)