HOUKEA BEE VENOM MOLE WART REMOVER- glycerin spray

HOUKEA Bee Venom Mole Wart Remover by

Drug Labeling and Warnings

HOUKEA Bee Venom Mole Wart Remover 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 INGREDIENTS

APIS MELLIFERA VENOM,MENTHA PIPERITA LEAF,TOCOPHEROL

PURPOSE

Painlessly remove skin warts and moles; quickly remove skin tags and restore skin smoothness; remove various types of warts and improve skin texture.

USES

Spray an appropriate amount of this product evenly on the warts or moles and wait for it to be 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.

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

GLYCERIN、SALICYLIC ACID

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA BEE VENOM MOLE WART REMOVER 
glycerin spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-104
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHA PIPERITA LEAF (UNII: A389O33LX6) (MENTHA PIPERITA LEAF - UNII:A389O33LX6)	MENTHA PIPERITA LEAF	3 mg  in 30 mg
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	9 mg  in 30 mg
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	4.5 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	9 mg  in 30 mg
SALICYLIC ACID (UNII: O414PZ4LPZ)	4.5 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-104-01	30 mg in 1 BOX; Type 0: Not a Combination Product	11/02/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	11/02/2024

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(84660-104)