SOUTH MOON Soothing Pain Relief Massage Gel

Manufacturer
Shantou South Moon Biotechnology Co., Ltd.
Effective date
2025-11-27
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:18:23

Label at a glance#

ProductSOUTH MOON Soothing Pain Relief Massage Gel
Active ingredientARTEMISIA ARGYI LEAF, GINGER
Label structure10 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ARTEMISIA ARGYI LEAF、GINGER

OTC - WHEN USING SECTION

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

OTC - PURPOSE SECTION

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

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Please keep out of reach of children. Do not swallow.

WARNINGS SECTION

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 SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

WATER、GLYCERIN、CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE、TROLAMINE、ALLANTOIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GINGER Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128SO-B04-0195-02SO-B04-0195-02(1).jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84983-007-01SOUTH MOON Soothing Pain Relief Massage Gel50 mg in 1 BOTTLEGEL502

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84983-00784983-007-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
449ef0fa-25ae-9611-e063-6394a90a6dbb33965722-8969-cca3-e063-6394a90a3c612025-11-27WarningsExact identifier
spl id: 449ef0fa-25ae-9611-e063-6394a90a6dbb
spl set id: 33965722-8969-cca3-e063-6394a90a3c61

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.