WART REMOVER PATCHES

Manufacturer
Hengyang Chuangjiujia Trading Co., Ltd.
Effective date
2025-07-22
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 01:08:13

Label at a glance#

ProductWART REMOVER PATCHES
Active ingredientSALICYLIC ACID
Label structure10 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 10%

OTC - PURPOSE SECTION

WART REMOVER

INDICATIONS & USAGE SECTION

Clear The Skin Tag

WARNINGS SECTION

For external use only.

OTC - WHEN USING SECTION

Keep out of reach of children Avoid contact with eyes.

OTC - STOP USE SECTION

Discontinue use if signs of irritation or rash occur.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children

DOSAGE & ADMINISTRATION SECTION

Directions Of Safe Use: 1.wash affected area and dry thoroughly. 2. apply tag patch. 3. after 24hours, remove tag patch. 4. repeat procedure every 24 hours for up to 14 days for tags removal and upto 12 weeks for tags, until the problem hascleared. 5.may hot compress wart in warm water for 5 minutesto assist in removal. 6. Store unused tag patch in a cool, dry place.

INACTIVE INGREDIENT SECTION

Tea Tree Oil
Calendula
Cica Oil
Castor Oil
Argan Oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2707561salicylic acid 10 % Medicated PatchPSN4
2707561salicylic acid 0.1 MG/MG Medicated PatchSCD4
2707561salicylic acid 10 % Medicated PatchSY4

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
dea2eded-d1e7-46bb-9a3d-f8dc20de6277Product name120190408

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
84735-003-01WART REMOVER PATCHES144 in 1 BAGPATCH1444

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84735-00384735-003-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3a8182e6-590f-cd72-e063-6394a90aa03b2fa88065-4d8e-777c-e063-6394a90a43212025-07-22WarningsExact identifier
spl id: 3a8182e6-590f-cd72-e063-6394a90aa03b
spl set id: 2fa88065-4d8e-777c-e063-6394a90a4321

Reported adverse events (FAERS/openFDA)#

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