FDA.reportPublic FDA data

85593-127-01 AOUGK SALICYLIC ACID WART REMOVER GEL

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2026-09-11
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-09-15 03:02:27

Label at a glance#

ProductAOUGK SALICYLIC ACID WART REMOVER
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic Acid 17% w/w Purpose Wart remover

OTC - PURPOSE SECTION

Uses
·for the removal of common warts

·for the removal of plantar warts

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

WARNINGS SECTION

Warnings

For external use only.
Do not use on children under 2 years of age unless directed by a doctor

DOSAGE & ADMINISTRATION SECTION

Wash the affected area.

Soak thewart in warm water for 5 minutes

ifneededDry the skin thoroughlyGently squeeze the tube and applyone drop to fully cover the wart.Let the gel dry and form a clearprotective film·

Repeat 1-2 times daily until thewartis removed

INDICATIONS & USAGE SECTION

When using this product*avoid contact with eyesIf contact occurs flush thoroughwith water
Stop use and ask doctor if
irritation develops·condition worsens

INACTIVE INGREDIENT SECTION

Inactive ingredients

Alcohol, Castor Oil, HydroxypropylCellulose, Camphor, Polysorbate80, Lactic Acid

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85593-127-0185593-127-01

Products#

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

DailyMed product names page 1 of 1 · 8 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-12785593-127-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
POLYSORBATE 806OZP39ZG8HIACT
HYDROXYPROPYL CELLULOSE, UNSPECIFIED9XZ8H6N6OHIACT
LACTIC ACID33X04XA5ATIACT
CAMPHOR (SYNTHETIC)5TJD82A1ETIACT
CASTOR OILD5340Y2I9GIACT
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-09-05daily-update2026-09-08 02:02:07

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
5ac88b51-b46d-5cc6-e063-6394a90af9e55ac88b51-b46c-5cc6-e063-6394a90af9e52026-09-05WarningsExact identifier
spl set id: 5ac88b51-b46c-5cc6-e063-6394a90af9e5

Reported adverse events (FAERS/openFDA)#

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