HOUKEA FOOT BATH BEADS- glycerin liquid

HOUKEA Foot Bath Beads by

Drug Labeling and Warnings

HOUKEA Foot Bath Beads 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)

LITHOSPERMUM ERYTHRORHIZON ROOT、MENTHA PIPERITA LEAF、 TOCOPHEROL

Purpose

Promote metabolism and blood circulation; relieve varicose veins; lift and tighten skin; accelerate fat decomposition

Use

Take out one ofthe products and put it into a container suitable for foot soaking, and add warm water of 40-50 degrees. After the product is completely dissolved, soak your feet in it and let it stand for 15-30 minutes. After soaking, dry your feet.

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.

SAFE HANDLING WARNING

Store in a cool and dry place.

INACTIVE INGREDIENT

GLYCERIN、ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA FOOT BATH BEADS 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-102
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	1 mg  in 10 mg
LITHOSPERMUM ERYTHRORHIZON ROOT (UNII: 9I70D8O47I) (LITHOSPERMUM ERYTHRORHIZON ROOT - UNII:9I70D8O47I)	LITHOSPERMUM ERYTHRORHIZON ROOT	2 mg  in 10 mg
MENTHA PIPERITA LEAF (UNII: A389O33LX6) (MENTHA PIPERITA LEAF - UNII:A389O33LX6)	MENTHA PIPERITA LEAF	1 mg  in 10 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	4 mg  in 10 mg
ALLANTOIN (UNII: 344S277G0Z)	2 mg  in 10 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-102-01	10 mg in 1 BOX; Type 1: Convenience Kit of Co-Package	11/01/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	11/01/2024

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(84660-102)