HOUKEA WART CORN CARE LIQUID- glycerin liquid

HOUKEA Wart Corn Care Liquid by

Drug Labeling and Warnings

HOUKEA Wart Corn Care Liquid by is a Otc medication manufactured, distributed, or labeled by Guangzhou Houkea Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

APIS MELLIFERA VENOM、MENTHA PIPERITA LEAF

WHEN USING

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

PURPOSE

Exfoliates; removes warts; soothes skin discomfort; reduces skin irritation and redness; restores skin smoothness

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.

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.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

WATER、GLYCERIN、HYDROXYETHYL CELLULOSE、ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA WART CORN CARE LIQUID 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84984-004
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
MENTHA PIPERITA LEAF (UNII: A389O33LX6) (MENTHA PIPERITA LEAF - UNII:A389O33LX6)	MENTHA PIPERITA LEAF	0.004 mg  in 20 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	1.6 mg  in 20 mg
HYDROXYMETHYL CELLULOSE (UNII: 273FM27VK1)	0.1 mg  in 20 mg
ALLANTOIN (UNII: 344S277G0Z)	0.004 mg  in 20 mg
WATER (UNII: 059QF0KO0R)	18.288 mg  in 20 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84984-004-01	20 mg in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		04/12/2025

Labeler - Guangzhou Houkea Biotechnology Co., Ltd. (456717258)

Registrant - Guangzhou Houkea Biotechnology Co., Ltd. (456717258)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Houkea Biotechnology Co., Ltd.		456717258	manufacture(84984-004)