FDA.reportPublic FDA data

South Moon Bee Venom Psoriasis Treatment

Manufacturer
Guangdong Ouhoe Biotechnology Co., Ltd.
Effective date
2024-10-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:25:30

Label at a glance#

ProductSouth Moon Bee Venom Psoriasis Treatment
Active ingredientAPIS MELLIFERA VENOM, MENTHA PIPERITA LEAF
Label structure10 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

Active Ingredient(s)

OTC - ACTIVE INGREDIENT SECTION

APIS MELLIFERA VENOM，MENTHA PIPERITA LEAF

Purpose

OTC - PURPOSE SECTION

Quickly relieve psoriasis symptoms

Use

OTC - WHEN USING SECTION

Relieve skin itching; relieve skin；discomfort caused by psoriasis;inhibit skin inflammation

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、 ALLANTOIN、 TOCOPHEROL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84744-010-01South Moon Bee Venom Psoriasis Treatment20 g in 1 BOXSPRAY201

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84744-010SOUTH MOON BEE VENOM PSORIASIS TREATMENT (APIS MELLIFERA VENOM) SPRAY [GUANGDONG OUHOE BIOTECHNOLOGY CO., LTD.]11 package rows20241017_058fd5b4-9aa0-4043-a429-5fc88bef6bf3.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
84744-01084744-010-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
APIS MELLIFERA VENOM76013O881MACTIB
MENTHA PIPERITA LEAFA389O33LX6ACTIM
GLYCERINPDC6A3C0OXIACT
ALLANTOIN344S277G0ZIACT
TOCOPHEROLR0ZB2556P8IACT

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
89e9b5b7-d37e-4614-a3d8-23115b65828e058fd5b4-9aa0-4043-a429-5fc88bef6bf32024-10-16WarningsExact identifier
spl id: 89e9b5b7-d37e-4614-a3d8-23115b65828e
spl set id: 058fd5b4-9aa0-4043-a429-5fc88bef6bf3

Reported adverse events (FAERS/openFDA)#

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