LIQUID WART CORN CALLUS REMOVER- angelica dahurica root liquid

liquid Wart Corn Callus Remover by

Drug Labeling and Warnings

liquid Wart Corn Callus Remover by is a Otc medication manufactured, distributed, or labeled by Guangzhou Mizi Biotechnology Co., LTD.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ANGELICA DAHURICA ROOT 2%
ASIATIC ACID 0.5%

PURPOSE

wart removal

INDICATIONS & USAGE

Liquid Wart Corn & Callus Remover

WARNINGS

For external use only.

DO NOT USE

1.Do not use on irritated skin or on any area that is infected or reddened.
2.lf you are allergic to any of the ingredients in this product.
3.On moles, birthmarks, warts with hairs growing from them,genital warts or warts on the face or mucous membranes

WHEN USING

When using this product, avoid contact with eyes. lf product gets into the eye,flush with water for 15 minutes
Cap bottle tightly and store at room temperature away from heat.

STOP USE

STOP USE AND SEE A DOCTOR IF:
You become pregnant, or are planning to become pregnant, while using the product.
if discomfort persists.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. lf swallowed, get medical help or contact Poison Control Center right away

DOSAGE & ADMINISTRATION

1.Soak for 5 minutes in warm water.
2.Insert the brush in the bottle
3.Apply the liquid to the desired area.
4.Apply it 2 times daily to enjoy your clean skin.

INACTIVE INGREDIENT

Aqua, Benzoic Acid, Propylene Glycol, Alcohol Denat, Acetic Acid

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIQUID WART CORN CALLUS REMOVER 
angelica dahurica root liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 84896-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ANGELICA DAHURICA ROOT (UNII: 1V63N2S972) (ANGELICA DAHURICA ROOT - UNII:1V63N2S972)	ANGELICA DAHURICA ROOT	0.02 g  in 1 mL
ASIATIC ACID (UNII: 9PA5A687X5) (ASIATIC ACID - UNII:9PA5A687X5)	ASIATIC ACID	0.005 g  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ACETIC ACID (UNII: Q40Q9N063P)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
AQUA (UNII: 059QF0KO0R)
BENZOIC ACID (UNII: 8SKN0B0MIM)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 84896-002-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	11/27/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		11/27/2025

Labeler - Guangzhou Mizi Biotechnology Co., LTD. (418001649)

Establishment
Name	Address	ID/FEI	Business Operations
Guangzhou Mizi Biotechnology Co., LTD.		418001649	manufacture(84896-002)