WART REMOVER

Manufacturer: Guangdong Jiaoyu Biotechnology Co., Ltd
Effective date: 2026-08-10
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: daily-update
Hydrated at: 2026-08-12 01:01:13

Label at a glance#

ProductWART REMOVER

Active ingredientSALICYLIC ACID

Label structure8 sections

Label contents#

Full prescribing information#

WARNINGS SECTION

Keep out of reach of children after use

INACTIVE INGREDIENT SECTION

WATER
GLYCERIN

INDICATIONS & USAGE SECTION

1.For external application only

2.Wash the affected areas;Soak the wart in warm water for 5 minutes and dry thoroughly

Apply one drop at a time to cover the affected area completely and allow to dry; Repeat once or twice daily as needed for up to12 weeks

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of children's reach at all times

OTC - PURPOSE SECTION

WART REMOVER

DOSAGE & ADMINISTRATION SECTION

Salicylic Acid 17% w/w

RECENT MAJOR CHANGES SECTION

Salicylic Acid 17% w/w

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1 1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

WART REMOVER
SALICYLIC ACID
WATER

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
87722-067	87722-067-03

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
SALICYLIC ACID	O414PZ4LPZ	ACTIB
WATER	059QF0KO0R	IACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
WART REMOVER	SALICYLIC ACID	Guangdong Jiaoyu Biotechnology Co., Ltd	58b3cc68-bbde-ef94-e063-6394a90a37bb	2026-08-10	Warnings	Exact identifier ndc (package): 87722-067-03 ndc (product): 87722-067 ndc11 (package): 87722006703 spl id: 58b3c830-9d08-ec43-e063-6394a90a75eb spl set id: 58b3cc68-bbde-ef94-e063-6394a90a37bb

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.