XIMONTH BEE VENOM REPAIR- glycerin liquid

XIMONTH Bee Venom Repair by

Drug Labeling and Warnings

XIMONTH Bee Venom Repair 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

APIS MELLIFERA VENOM

WHEN USING

1. Clean and dry skin

2. Spray directly on the affected area with the spray

3. Gently massage until absorbed

PURPOSE

1. Can quickly and safely remove all kinds of skin tags and warts without pain and scars.

2. It can lighten spots, lighten uneven skin tone, repair damaged skin, and make your skin softer and fairer.

3. The gentle and safe formula brings gentle care and peace of mind to your skin.

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.

STOP USE

Discontinue use if signs of irritation or rash occur.

DO NOT 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

AQUA、ACETIC ACID、GLYCERIN、TRIAZOCARBONIC ACID

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

XIMONTH BEE VENOM REPAIR 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84989-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	0.004 mg  in 20 mg

Inactive Ingredients
Ingredient Name	Strength
AQUA (UNII: 059QF0KO0R)	18.396 mg  in 20 mg
TRIAZOLAM (UNII: 1HM943223R)	0.2 mg  in 20 mg
GLYCERIN (UNII: PDC6A3C0OX)	0.4 mg  in 20 mg
ACETIC ACID (UNII: Q40Q9N063P)	1 mg  in 20 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84989-006-01	20 mg in 1 BOX; Type 0: Not a Combination Product	06/19/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	06/19/2025

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(84989-006)