SOUTH MOON WART REMOVER- glycerin liquid

SOUTH MOON Wart Remover by

Drug Labeling and Warnings

SOUTH MOON Wart Remover by is a Otc medication manufactured, distributed, or labeled by Shantou South Moon Biotechnology Co., Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

CENTELLA ASIATICA TRITERPENOIDS、HAMAMELIS VIRGINIANA LEAF WATER、ALOE BARBADENSIS LEAF

WHEN USING

1. Clean skin thoroughly and dry first

2. Take an appropriate amount of this product and apply it on the skin where warts grow.

PURPOSE

1. Easily remove skin tags, painlessly remove skin warts and moles, and quickly restore smooth skin.

2. The formula is mild and suitable for all types of skin, making it safer to use.

3. Use tea tree oil and saffron plant ingredients to protect and care for the skin.

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. Do not swallow.

STORAGE AND HANDLING

Store in a cool and dry place.

INACTIVE INGREDIENT

AQUA、GLYCERIN

DOSAGE & ADMINISTRATION

1. Clean skin thoroughly and dry first

2. Take an appropriate amount of this product and apply it on the skin where warts grow.

INDICATIONS & USAGE

Take an appropriate amount of this product and apply it on the skin where warts grow.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SOUTH MOON WART REMOVER 
glycerin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84983-013
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J) (CENTELLA ASIATICA TRITERPENOIDS - UNII:4YS74Q4G4J)	CENTELLA ASIATICA TRITERPENOIDS	0.01 mg  in 10 mg
HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER (UNII: 8FP93ED6H2) (HAMAMELIS VIRGINIANA LEAF WATER - UNII:8FP93ED6H2)	HAMAMELIS VIRGINIANA (WITCH HAZEL) LEAF WATER	0.002 mg  in 10 mg
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X) (ALOE BARBADENSIS LEAF - UNII:ZY81Z83H0X)	ALOE BARBADENSIS LEAF	0.002 mg  in 10 mg

Inactive Ingredients
Ingredient Name	Strength
AQUA (UNII: 059QF0KO0R)	9.486 mg  in 10 mg
GLYCERIN (UNII: PDC6A3C0OX)	0.5 mg  in 10 mg

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84983-013-01	10 mg in 1 BOTTLE; Type 0: Not a Combination Product	09/17/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/17/2025

Labeler - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Registrant - Shantou South Moon Biotechnology Co., Ltd. (457126192)

Establishment
Name	Address	ID/FEI	Business Operations
Shantou South Moon Biotechnology Co., Ltd.		457126192	manufacture(84983-013)