SOUTH MOON PROPOLIS PROFESSIONAL TREATMENT GEL- allantoin gel

SOUTH MOON Propolis Professional Treatment Gel by

Drug Labeling and Warnings

SOUTH MOON Propolis Professional Treatment Gel by is a Otc medication manufactured, distributed, or labeled by Guangdong Ximonth Technology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient(s)

GLUCOSE、CURCUMIN、EICOSAPENTAENOIC ACID、CHOLECALCIFEROL

Purpose

1.His product contains a variety of active ingredients to promote blood circulation, relieve arthritis pain,and eliminate joint inflammation.
2.Liminate cysts and edema,promote joint tissue repair,improve joint elasticity and mobility.
3.The texture is refreshing and non-greasy, easy to be absorbed by the skin. Deep penetration to solve various joint problems.
4.Convenient to use, long-lasting effect, safe and does not hurt the skin.

Use

1.Clean the skin and dry it.
2.Take an appropriate amount of this product and apply it evenly on the joint skin discomfort.
3.Gently massage until fully absorbed(It is recommended to use 2-3 times a day to achieve better results)

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.

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.

STORAGE AND HANDLING

Avoid freezing and excessive heat above 40C (104F) ）
Store in a cool and dry place.

INACTIVE INGREDIENT

ALLANTOIN

DOSAGE & ADMINISTRATION

INDICATIONS & USAGE

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON PROPOLIS PROFESSIONAL TREATMENT GEL 
allantoin gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84660-034
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK) (ANHYDROUS DEXTROSE - UNII:5SL0G7R0OK)	ANHYDROUS DEXTROSE	5 g  in 20 g
CURCUMIN (UNII: IT942ZTH98) (CURCUMIN - UNII:IT942ZTH98)	CURCUMIN	4 g  in 20 g
ICOSAPENT (UNII: AAN7QOV9EA) (ICOSAPENT - UNII:AAN7QOV9EA)	ICOSAPENT	3 g  in 20 g
CHOLECALCIFEROL (UNII: 1C6V77QF41) (CHOLECALCIFEROL - UNII:1C6V77QF41)	CHOLECALCIFEROL	2 g  in 20 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)	6 g  in 20 g

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84660-034-01	20 g in 1 BOX; Type 0: Not a Combination Product	09/27/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/27/2024

Labeler - Guangdong Ximonth Technology Co., Ltd. (699436264)

Registrant - Guangdong Ximonth Technology Co., Ltd. (699436264)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ximonth Technology Co., Ltd.		699436264	manufacture(84660-034)