SOUTH MOON BEE VENOM TREATMENT SERUM- glycerin liquid

SOUTH MOON Bee Venom Treatment Serum by

Drug Labeling and Warnings

SOUTH MOON Bee Venom Treatment Serum by is a Otc medication manufactured, distributed, or labeled by Guangdong Ouhoe Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENTS

APIS MELLIFERA VENOM，
TEA TREE OIL,
ALOE VERA LEAF,
TOCOPHEROL

PURPOSE

Repair damaged and discolorednails;improve cracked and cracked nailshelps keep away fungal naildiseases.

USE

Take anappropriate amount of this product and apply it evenly on the nails and periungual skin, wait for 2-3 minutesbefore it is completely absorbed

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.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

TOCOPHEROL

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON BEE VENOM TREATMENT SERUM 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	9 mg  in 30 mg
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	4.5 mg  in 30 mg
ALOE VERA LEAF (UNII: ZY81Z83H0X) (ALOE VERA LEAF - UNII:ZY81Z83H0X)	ALOE VERA LEAF	4.5 mg  in 30 mg
TEA TREE OIL (UNII: VIF565UC2G) (TEA TREE OIL - UNII:VIF565UC2G)	TEA TREE OIL	3 mg  in 30 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	9 mg  in 30 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-011-01	30 mg in 1 BOX; Type 0: Not a Combination Product	10/17/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	10/17/2024

Labeler - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Registrant - Guangdong Ouhoe Biotechnology Co., Ltd. (843651433)

Establishment
Name	Address	ID/FEI	Business Operations
Guangdong Ouhoe Biotechnology Co., Ltd.		843651433	manufacture(84744-011)