HOUKEA BUNIONS CORRECTION PATCH- glycerin patch

HOUKEA Bunions Correction Patch by

Drug Labeling and Warnings

HOUKEA Bunions Correction Patch 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 Ingredient(s)

APIS MELLIFERA VENOM、TEA TREE OIL、TOCOPHEROL、ALOE VERA LEAF

Purpose

Relieves bunions by preventing joint flexion; dissolves fluid accumulation in joints and restores toe health; repairs tissue and restores toe mobility

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.

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.

Use

Peel off the adhesive backing and wrap the patch around your thumb, adhering securely to the joint.

INACTIVE INGREDIENT

GLYCERIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA BUNIONS CORRECTION PATCH 
glycerin patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-084
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	2.5 g  in 10 g
TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G)	TEA TREE OIL	2 g  in 10 g
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	1.5 g  in 10 g
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	1 g  in 10 g

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	3 g  in 10 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-084-01	10 g in 1 BOX; Type 1: Convenience Kit of Co-Package	10/23/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	10/23/2024

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(84660-084)