SOUTH MOON Magnesium Soothing Cream

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 01:18:29

Label at a glance#

ProductSOUTH MOON Magnesium Soothing Cream
Active ingredientLAVENDER OIL, MENTHA SUAVEOLENS LEAF, ALOE VERA LEAF
Label structure12 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

MENTHA SUAVEOLENS LEAF、LAVENDER OIL、ALOE VERA LEAF

OTC - PURPOSE SECTION

1. Deeply moisturize the skin, replenish the skin's moisture barrier and prevent moisture loss.

2. Enhance the skin's water-locking ability, repair and nourish the skin at night, so that the skin can be fully hydrated and moisturized during the rest period.

3. Enhance the hydration of the skin, keep the skin moist and plump for a long time, improve dryness and roughness, and make the skin look healthier and shiny.

OTC - WHEN USING SECTION

Relieve nerve pain and promote blood circulation; deeply nourish the skin and improve dry skin; enhance skin vitality and provide a relaxing experience.

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.

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.

STORAGE AND HANDLING SECTION

Store in a cool and dry place.

INACTIVE INGREDIENT SECTION

WATER、GLYCERIN、MINERAL OIL、GLYCERYL MONOSTEARATE、1,2-HEXANEDIOL、CARBOMER HOMOPOLYMER TYPE A 、TROLAMINE、ALLANTOIN、MAGNESIUM CHLORIDE

INDICATIONS & USAGE SECTION

Relieve nerve pain and promote blood circulation; deeply nourish the skin and improve dry skin; enhance skin vitality and provide a relaxing experience.

DOSAGE & ADMINISTRATION SECTION

Relieve nerve pain and promote blood circulation; deeply nourish the skin and improve dry skin; enhance skin vitality and provide a relaxing experience.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128SO-A06-0068-01SO-A06-0068-01.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84983-018-01SOUTH MOON Magnesium Soothing Cream120 mg in 1 BOTTLE, PLASTICCREAM1202

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84983-01884983-018-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
449f03f4-fa2b-68a1-e063-6294a90a68db42d737a1-5ea3-4801-e063-6294a90af1af2025-11-27WarningsExact identifier
spl id: 449f03f4-fa2b-68a1-e063-6294a90a68db
spl set id: 42d737a1-5ea3-4801-e063-6294a90af1af

Reported adverse events (FAERS/openFDA)#

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