SOUTH MOON Corn Removal Plaster

Manufacturer
Guangdong Ximonth Technology Co., Ltd.
Effective date
2024-11-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:34:03

Label at a glance#

ProductSOUTH MOON Corn Removal Plaster
Active ingredientGLYCYRRHIZA GLABRA, SAFFLOWER, ALOE VERA LEAF, SOPHORA FLAVESCENS ROOT
Label structure9 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

SOPHORA FLAVESCENS ROOT、SAFFLOWER、GLYCYRRHIZA GLABRA、ALOE VERA LEAF

Use

OTC - WHEN USING SECTION

1.Cleanse and dry the affected area.
2.Apply the cream to the surrounding skin Cream.
3.Apply it 2 times Daily.

Warnings

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.

Do not use

OTC - DO NOT USE SECTION

Discontinue use if signs of irritation or rash occur.

Stop Use

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

GLYCERIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
GLYCYRRHIZA GLABRA Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84660-062-01SOUTH MOON Corn Removal Plaster16 g in 1 BOXPLASTER161

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84660-062SOUTH MOON CORN REMOVAL PLASTER (GLYCERIN) PLASTER [GUANGDONG XIMONTH TECHNOLOGY CO., LTD.]11 package rows20241106_25e9c088-5a77-c761-e063-6394a90ab8a2.zip

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84660-06284660-062-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 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
25e9c088-5a78-c761-e063-6394a90ab8a225e9c088-5a77-c761-e063-6394a90ab8a22024-11-02WarningsExact identifier
spl id: 25e9c088-5a78-c761-e063-6394a90ab8a2
spl set id: 25e9c088-5a77-c761-e063-6394a90ab8a2

Reported adverse events (FAERS/openFDA)#

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