ZRIZL WART REMOVER- salicylic acid liquid

ZRIZL wart Remover by

Drug Labeling and Warnings

ZRIZL 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

Salicylic acid 8% w/w

PURPOSE

Uses For The removai ol s corns, calluses, piantar warts, filat warts, comman warts (less than 5 mmin stze)

WARNINGS

Warnings o For exernal use only ，Keep away fromheat or flame

KEEP OUT OF REACH OF CHILDREN

Keep out of reach ofchildren, lfswallowed, get medical help or contact a Poison controt center right a-way

DOSAGE & ADMINISTRATION

Wash the affected area ， Soak the.wartsin warm water for 5 minutes aind dryit thoroughly Apply one drop at a time with the applicator to cov.er the warts completely o Allow to dry, use self adhesive cushloning pads to cover the warts if deslred@Repeat this pracess once or twice dally as neededfor up to 12 weeks, until the warts is removed (Nte.For external use, and can not be applied to healthy skin)

INACTIVE INGREDIENT

ALCOHOL
SOPHORA FLAVESCENS ROOT
LITHOSPERMUM INCISUM WHOLEANGELICA DAHURICA VAR. FORMOSANA WHOLEBRUCEA JAVANICA WHOLE

INDICATIONS & USAGE

keep out of eyes, ear ;and mouth if product gets in eyes, flush with waterfor 15 minutes

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ZRIZL WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 85593-015
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
ALCOHOL (UNII: 3K9958V90M)
ANGELICA DAHURICA VAR. FORMOSANA WHOLE (UNII: 247A107296)
LITHOSPERMUM INCISUM WHOLE (UNII: 0WMC2EKY2U)
SOPHORA FLAVESCENS ROOT (UNII: IYR6K8KQ5K)
BRUCEA JAVANICA WHOLE (UNII: Z4CCI5NZ66)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 85593-015-01	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/15/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M028	09/15/2025

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

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