BEE VENOM TREATMENT CREAM cream

BEE VENOM TREATMENT Cream by

Drug Labeling and Warnings

BEE VENOM TREATMENT Cream 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

Inactive ingredient

Cypress Leaf Extract /5 Percent salicylic acid / Borneol/Mint / Tea tree oil

Purpose section

1. Natural & safe ingredients

2. lmmediate action & relaxation

3. Gently nourishes skin
4. For all mature skin types

5. Rebuild skin confidence andimprove quality of life,

Warning

1. Please use according to the instructions

2. if it accidentally gets into your eyes, please rinse with waterimmediately.
3. lf there are any abnormalities on your skin, please stop using it.

4. Please keep out of reach of children. Prevent children fromaccidentally swallowing, and pregnant women should use withcaution.

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

Step 1: Clean and dry skin
Step 2: Open the cap and applyto the affectedarea with your handsor a cotton swab
Step 3: Gently massage until absorbed

DOSAGE

As fast as 3 days to fall off

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

BEE VENOM TREATMENT CREAM 
bee venom treatment cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84732-065
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 100 g

Inactive Ingredients
Ingredient Name	Strength
TEA TREE OIL (UNII: VIF565UC2G)
CUPRESSUS SEMPERVIRENS LEAF (UNII: T3G9Z77187)
SALICYLIC ACID (UNII: O414PZ4LPZ)
MINT (UNII: FV98Z8GITP)
BORNEOL (UNII: M89NIB437X)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84732-065-01	30 g in 1 BOTTLE; 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(84732-065)