SOUTH MOON SOOTHING PAIN RELIEF MASSAGE GEL- glycerin gel

SOUTH MOON Soothing Pain Relief Massage Gel by

Drug Labeling and Warnings

SOUTH MOON Soothing Pain Relief Massage Gel by is a Otc medication manufactured, distributed, or labeled by Shantou South Moon Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ARTEMISIA ARGYI LEAF、GINGER

WHEN USING

Clean and dry skin, apply appropriate amount of this product to the affected area, massage for absorption.

PURPOSE

Relieve arthritis pain; improve joint flexibility and mobility; relieve muscle stiffness and discomfort.

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、CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE、TROLAMINE、ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON SOOTHING PAIN RELIEF MASSAGE GEL 
glycerin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84983-007
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARTEMISIA ARGYI LEAF (UNII: 2JYC99Q0WZ) (ARTEMISIA ARGYI LEAF - UNII:2JYC99Q0WZ)	ARTEMISIA ARGYI LEAF	0.01 mg  in 50 mg
GINGER (UNII: C5529G5JPQ) (GINGER - UNII:C5529G5JPQ)	GINGER	0.01 mg  in 50 mg

Inactive Ingredients
Ingredient Name	Strength
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)	0.1 mg  in 50 mg
TROLAMINE (UNII: 9O3K93S3TK)	0.1 mg  in 50 mg
ALLANTOIN (UNII: 344S277G0Z)	0.01 mg  in 50 mg
WATER (UNII: 059QF0KO0R)	45.77 mg  in 50 mg
GLYCERIN (UNII: PDC6A3C0OX)	4 mg  in 50 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84983-007-01	50 mg in 1 BOTTLE; Type 0: Not a Combination Product	04/25/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	04/25/2025

Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou South Moon Biotechnology Co., Ltd.		457126192	manufacture(84983-007)