SOUTH MOON MELITTIN JOINT SOOTHING GEL gel

SOUTH MOON Melittin Joint Soothing Gel by

Drug Labeling and Warnings

SOUTH MOON Melittin Joint Soothing Gel by is a Otc medication manufactured, distributed, or labeled by Dongguan Haiyi Technology Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

BEE VENOM

GLUCOSAMINE

Inactive ingredient

AQUA,CURCUMIN,EICOSAPENTAENOIC ACID,CHOLE-CALCIFEROL

Purpose section

1.Solve various joint problems

2.passed the USA FDAapproved

3.Effectively relieves arthritis pain

4.Does not contain anyharmful ingredients.

Warning

Please keep out of reachof children. Do notswallow.Please clean yourhands before use to ensurethe best results from theproduct. Discontinue useif signs of irritation or rashoccur. Store in a cool and dry place.

stop use

This product may cause allergic reactions in asmall number of people.
lf youexperience any discomfort,please stop using it immediately.

not use

Not suitable for use by children, pregnantor breast feeding people.

OUT OF CHILDREN

KEEP THE PRODUCT OUT OF REACH OF CHILDREN to

HOW TO USE

1. Clean and dry the skin onthe joints.

2. Take an appropriateamount of gel and apply itevenly on the joints.

3. Gently massage withhands in circular motionuntil absorbed.

4. Daily use can get betterresults.

Dosage

take an appropriateamount,Use 2-3 times a week

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON MELITTIN JOINT SOOTHING GEL 
south moon melittin joint soothing gel gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-055
Route of Administration	CUTANEOUS

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	1 mg  in 20 g
GLUCOSAMINE (UNII: N08U5BOQ1K) (GLUCOSAMINE - UNII:N08U5BOQ1K)	GLUCOSAMINE	1 mg  in 20 g

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
CURCUMIN (UNII: IT942ZTH98)
CHOLECALCIFEROL (UNII: 1C6V77QF41)
ICOSAPENT (UNII: AAN7QOV9EA)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-055-01	20 g in 1 TUBE; Type 0: Not a Combination Product	10/21/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/21/2024

Labeler - Dongguan Haiyi Technology Co.,Ltd. (722030807)

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-055)