SOUTH MOON BEE VENOM CREAM- glycerin cream

SOUTH MOON Bee Venom Cream by

Drug Labeling and Warnings

SOUTH MOON Bee Venom Cream by is a Otc medication manufactured, distributed, or labeled by Shantou South Moon Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

BEE VENOM

WHEN USING

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.

PURPOSE

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.

DO NOT USE

Discontinue use if signs of irritation or rash occur.

STOP USE

Discontinue use if signs of irritation or rash occur.

KEEP OUT OF REACH OF CHILDREN

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

WARNINGS

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

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA
MINERAL OIL
GLYCERIN
GLYCERYL STEARATE
CARBOMER
ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON BEE VENOM CREAM 
glycerin cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84983-006
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	0.006 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	0.9 mg  in 30 mg
MINERAL OIL (UNII: T5L8T28FGP)	3 mg  in 30 mg
CARBOMER (UNII: 0A5MM307FC)	0.06 mg  in 30 mg
GLYCERYL STEARATE (UNII: 230OU9XXE4)	0.6 mg  in 30 mg
AQUA (UNII: 059QF0KO0R)	25.428 mg  in 30 mg
ALLANTOIN (UNII: 344S277G0Z)	0.006 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84983-006-01	30 mg in 1 BOX; Type 0: Not a Combination Product	04/14/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	04/14/2025

Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou South Moon Biotechnology Co., Ltd.		457126192	manufacture(84983-006)