Bee Venmo Pain Cream by Shenzhenshishengyakeji Co., Ltd.

Bee Venmo Pain Cream by

Drug Labeling and Warnings

Bee Venmo Pain Cream by is a Otc medication manufactured, distributed, or labeled by Shenzhenshishengyakeji Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

BEE VENMO PAIN CREAM- bee venmo pain cream ointment 
Shenzhenshishengyakeji Co., Ltd.

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Bee Venom Extract：7.5 mg in 30 g
Arnica Chamissonis Flower Extract：4.5 mg in 30 g
Glucosamine：4.5 mg in 30 g
Menaquinone-7：4.5 mg in 30 g
Dimethyl Sulfone：4.5 mg in 30 g

soothe joints swelling,and reduce pain and discomfort.

Conditon worse or doesnot improve after regular use as directed

1.Clean and dry the affected area of skin.
2.Take an appropriate amount of cream and apply lt eyenly on the skin.
3.Massage gently with your hands in circular motions for absorption.
4.Use it 2-3 times a day for batter results.

Please clean your hands before use to ensure the best results from the product.

Please keep out of reach of chldren.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 niace.

soothe joints swelling,and reduce pain and discomfort.

Please keep out of reach of children.

Sodium Butyroyl/Formoyl Chondroitin Sulfate:4.5 mg in 30 g

BEE VENMO PAIN CREAM 
bee venmo pain cream ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84752-016
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) (DIMETHYL SULFONE - UNII:9H4PO4Z4FT)	DIMETHYL SULFONE	4.5 mg  in 30 g
MENAQUINONE-7 (UNII: 8427BML8NY) (MENAQUINONE-7 - UNII:8427BML8NY)	MENAQUINONE-7	4.5 mg  in 30 g
ARNICA CHAMISSONIS FLOWER EXTRACT (UNII: 88WK5I8R3L) (ARNICA CHAMISSONIS FLOWER EXTRACT - UNII:88WK5I8R3L)	ARNICA CHAMISSONIS FLOWER EXTRACT	4.5 mg  in 30 g
GLUCOSAMINE (UNII: N08U5BOQ1K) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE	4.5 mg  in 30 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM BUTYROYL/FORMOYL HYALURONATE (UNII: F63GOY24UQ)	4.5 mg  in 30 g

Product Characteristics
Color	green	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84752-016-01	30 g in 1 CANISTER; Type 0: Not a Combination Product	10/27/2024	12/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M020	10/27/2024	12/31/2024

Labeler - Shenzhenshishengyakeji Co., Ltd. (619715687)

Registrant - Shenzhenshishengyakeji Co., Ltd. (619715687)

Establishment
Name	Address	ID/FEI	Business Operations
Shenzhenshishengyakeji Co., Ltd.		619715687	label(84752-016)

Revised: 10/2024

Document Id: 256f4182-ace4-c6d2-e063-6394a90a4807

34390-5

Set id: 256f4182-ace3-c6d2-e063-6394a90a4807

Version: 1

Effective Time: 20241027