ADVANCED WART REMOVER- salicylic acid liquid

ADVANCED WART REMOVER by

Drug Labeling and Warnings

ADVANCED WART REMOVER by is a Otc medication manufactured, distributed, or labeled by Guangzhou ChuanMa International Trading Co.,Ltd.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active ingredientSalicylic acid 896
Purpose
Wart and corn remover

PURPOSE

Uses For The removal of skin tags, corns, calluses, plantar warts, flat warts, common warts (less than 5 mmin size).

WARNINGS

Warnings @For external use only @ Keep away fromheat or flame

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children, lfswallowed, get me.dical help or contact a Poison Control Center right a-Way.

DOSAGE & ADMINISTRATION

Directions @Wash the affected area @Soak the wartin warm water for 5 minutes and dry it thoroughlyApply one drop at a time with the applicator to cov.er the skin tag completely @ Allow to dry, use self-ad.hesive cushioning pads to cover the wart if desired@Repeat this process once or twice daily as needed,for up to 12 weeks, until the wart is removed (Note:For externat use, and can not be applied to healthy skin)

INACTIVE INGREDIENT

Inactive ingredients Brucea javanica, Radix Angelica,Lithospermum, Sophora, Antiseptic substance

INDICATIONS & USAGE

Wash the affected area Soak the wartin warm water for 5 minutes and dry it thoroughly

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ADVANCED WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85593-115
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	8 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ANGELICA SINENSIS ROOT (UNII: B66F4574UG)
LITHOSPERMUM ERYTHRORHIZON ROOT (UNII: 9I70D8O47I)
BRUCEA JAVANICA WHOLE (UNII: Z4CCI5NZ66)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85593-115-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/22/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	10/22/2025

Labeler - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)

Registrant - Guangzhou ChuanMa International Trading Co.,Ltd. (510247477)