BEE VENOM TREATMENT spray

Bee Venom Treatment by

Drug Labeling and Warnings

Bee Venom Treatment 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 Extract

Inactive ingredient

Melittin Apamin,Adolapin Aque, Salicylic Acid，Melaleluca Alternifolia Leaf oil.

Purpose section

The TagRecedeTreatment Spray is thesolution harness the potentproperties of bee venom to effectivelytarget various skin imperfections,including skin tags, moles, warts, andspots.infused with active compoundsextracted from bee venom, thisadvanced formula to break down andgently removing unwanted growths.

Warning

To avoid danger of suffocation,keepthis bag away from babies andchildren,Do not use this bag in cribs,beds, carriages,or play pens. THlS BAG IS NOT A TOY.

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. Start by thoroughly cleansing theskin area.

2. Press 1-2 pumps of thespray and distribute it evenly on theskin.

3. Gently massage in circularmotions with your hands to helpabsorption.

Dosage

take an appropriateamount,Use 2-3 times a week

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEE VENOM TREATMENT 
bee venom treatment spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-064
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 mL

Inactive Ingredients
Ingredient Name	Strength
MELITTIN (UNII: 24VT8NVE75)
SALICYLIC ACID (UNII: O414PZ4LPZ)
TEA TREE OIL (UNII: VIF565UC2G)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-064-01	20 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	10/25/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/25/2024

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

Establishment
Name	Address	ID/FEI	Business Operations
Dongguan Haiyi Technology Co.,Ltd.		722030807	manufacture(84732-064)