SOUTH MOON Bee Venom 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 01:18:23

Label at a glance#

ProductSOUTH MOON Bee Venom Cream
Active ingredientAPIS MELLIFERA VENOM
Label structure10 sections

Storage and handling

Store in a cool and dry place.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

BEE VENOM

OTC - WHEN USING SECTION

1. Clean skin and keep it dry

2. Take an appropriate amount of this product and apply it evenly on the affected joint skin.

3. Massage gently for complete absorption.

OTC - PURPOSE SECTION

1. Efficiently relieve joint discomfort and restore your joints to a healthy state.

2. Helps reduce swelling, restore joint vitality, and improve mobility.

3. The ingredients are mild, not irritating to the skin, and suitable for all types of skin.

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

AQUA
MINERAL OIL
GLYCERIN
GLYCERYL STEARATE
CARBOMER
ALLANTOIN

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeCode 128SOB04-A019-30-YE11(1).jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84983-006-01SOUTH MOON Bee Venom Cream30 mg in 1 BOXCREAM302

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
84983-00684983-006-01

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
449ef816-40f6-60be-e063-6294a90a97fa32ba0ec7-735b-bcb0-e063-6294a90aad8c2025-11-27WarningsExact identifier
spl id: 449ef816-40f6-60be-e063-6294a90a97fa
spl set id: 32ba0ec7-735b-bcb0-e063-6294a90aad8c

Reported adverse events (FAERS/openFDA)#

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