SOUTH MOON HERBAL JOINT PAIN BALM- glycerin cream

SOUTH MOON Herbal Joint Pain Balm by

Drug Labeling and Warnings

SOUTH MOON Herbal Joint Pain Balm by is a Otc medication manufactured, distributed, or labeled by Guangdong Ouhoe Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

LITHOSPERMUM ERYTHRORHIZON ROOT,ARNICA MONTANA FLOWER,ARTEMISIA VULGARIS ROOT

purpose

Relieve pain in finger joints;relieve discomfort in toe joints;reduce numbness and swelling, and enhance joint flexibility.

uses

Apply appropriate amount to painful ioints 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

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON HERBAL JOINT PAIN BALM 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-071
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LITHOSPERMUM ERYTHRORHIZON ROOT (UNII: 9I70D8O47I) (LITHOSPERMUM ERYTHRORHIZON ROOT - UNII:9I70D8O47I)	LITHOSPERMUM ERYTHRORHIZON ROOT	9 g  in 30 g
ARTEMISIA VULGARIS ROOT (UNII: 32MP823R8S) (ARTEMISIA VULGARIS ROOT - UNII:32MP823R8S)	ARTEMISIA VULGARIS ROOT	4.5 g  in 30 g
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) (ARNICA MONTANA FLOWER - UNII:OZ0E5Y15PZ)	ARNICA MONTANA FLOWER	3 g  in 30 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	9 g  in 30 g
GLYCERIN (UNII: PDC6A3C0OX)	4.5 g  in 30 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-071-01	30 g 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 Ouhoe Biotechnology Co., Ltd. (843651433)

Registrant - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ouhoe Biotechnology Co., Ltd.		843651433	manufacture(84744-071)