HOUKEA PREMIUM HERBAL COMFREY- glycerin cream

HOUKEA Premium Herbal Comfrey by

Drug Labeling and Warnings

HOUKEA Premium Herbal Comfrey 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

LITHOSPERMUM ERYTHRORHIZON ROOT,ARNICA MONTANA FLOWER

PURPOSE

Relieve joint and bone pain; restore joint health and vitality; strengthen blood circulation; improve skin inflammatory response.

USES

Apply appropriate amount to painful joints and muscles and massage gently to promote absorption.

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、ALLANTOIN、GLUCOSAMINE

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

HOUKEA PREMIUM HERBAL COMFREY 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-092
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	5 g  in 50 g
LITHOSPERMUM ERYTHRORHIZON ROOT (UNII: 9I70D8O47I) (LITHOSPERMUM ERYTHRORHIZON ROOT - UNII:9I70D8O47I)	LITHOSPERMUM ERYTHRORHIZON ROOT	15 g  in 50 g

Inactive Ingredients
Ingredient Name	Strength
GLUCOSAMINE (UNII: N08U5BOQ1K)	15 g  in 50 g
GLYCERIN (UNII: PDC6A3C0OX)	7.5 g  in 50 g
ALLANTOIN (UNII: 344S277G0Z)	7.5 g  in 50 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-092-01	50 g in 1 BOX; Type 0: Not a Combination Product	10/29/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	10/29/2024

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(84660-092)