SOUTH MONTH BEE VENOM NAIL FUNGUS REPAIRING LIQUID- glycerin liquid

SOUTH MONTH Bee Venom Nail Fungus Repairing Liquid by

Drug Labeling and Warnings

SOUTH MONTH Bee Venom Nail Fungus Repairing Liquid 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、MELALEUCA ALTERNIFOLIA LEAF、TOCOPHEROL、ALOE

purpose

Eliminates various types of fungal infections; strong antimicrobial properties to eliminate fungi; stimulate tissue regeneration; promote long-term prevention of infections

use

Use a brush to take an appropriate amount of this product and apply it evenly on the nail surface and surrounding skin. Just wait a few minutes for it to dry naturally.

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.

KEEP OUT OF REACH OF CHILDREN

Please keep out of reach of children. Do not swallow.

STOP USE

Discontinue use if signs of irritation or rash occur.

DO NOT USE

Discontinue use if signs of irritation or rash occur.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

GLYCERIN

INDICATIONS & USAGE

DOSAGE & ADMINISTRATION

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MONTH BEE VENOM NAIL FUNGUS REPAIRING LIQUID 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84744-063
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MELALEUCA ALTERNIFOLIA LEAF (UNII: G43C57162K) (MELALEUCA ALTERNIFOLIA LEAF - UNII:G43C57162K)	MELALEUCA ALTERNIFOLIA LEAF	1 mg  in 10 mg
TOCOPHEROL (UNII: R0ZB2556P8) (TOCOPHEROL - UNII:R0ZB2556P8)	TOCOPHEROL	1.5 mg  in 10 mg
APIS MELLIFERA VENOM (UNII: 76013O881M) (APIS MELLIFERA VENOM - UNII:76013O881M)	APIS MELLIFERA VENOM	3 mg  in 10 mg
ALOE (UNII: V5VD430YW9) (ALOE - UNII:V5VD430YW9)	ALOE	1.5 mg  in 10 mg

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)	3 mg  in 10 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84744-063-01	10 mg in 1 BOX; Type 0: Not a Combination Product	10/24/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M014	10/24/2024

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(84744-063)