FDA.reportPublic FDA data

SKIN TAG REMOVER

Manufacturer
Guangzhou ChuanMa International Trading Co.,Ltd.
Effective date
2025-11-14
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:16:05

Label at a glance#

ProductSKIN TAG REMOVER
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic acid

OTC - PURPOSE SECTION

for the removal of warts and tags

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children, lf swallowed, get medical help or contact aPoison Control Center(1-800-222-1222)right away.

WARNINGS SECTION

For external use only

DOSAGE & ADMINISTRATION SECTION

apply the patch directly over the wart or tag

repeat this procedure every 48 hours as needed, until the wart or tag is removedfor up to 12 weeks

INDICATIONS & USAGE SECTION

wash affected areadry area thoroughlyapply the patch directly over the wart or tagrepeat this procedure every 48 hours as needed, until the wart or tag is removed,for up to 12 weeks

INACTIVE INGREDIENT SECTION

Inactive ingredients Cellulose Gum, Propylene Glycol, Cyclodextrin, MelaleucaAlternifolia (Tea Tree) Leaf Oil, Centella Asiatica Extract, Polyisobutene,Hydroxyethylcellulose, Disodium Phosphate, polysorbate 60

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labelinglabeling

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2688287salicylic acid 15 % Medicated PatchPSN1
2688287salicylic acid 0.15 MG/MG Medicated PatchSCD1
2688287salicylic acid 15 % Medicated PatchSY1

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
85593-120-01SKIN TAG REMOVER144 in 1 BOXPATCH1441
85593-120-01SKIN TAG REMOVER1 g in 1 PATCHPATCH11

Products#

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

DailyMed product names page 1 of 1 · 11 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85593-12085593-120-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
SALICYLIC ACIDO414PZ4LPZACTIB
DISODIUM PHOSPHATE22ADO53M6FIACT
CYCLODEXTRIN7E6SK9QDT8IACT
CENTELLA ASIATICA7M867G6T1UIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
CELLULOSE GUMK679OBS311IACT
HYDROXYETHYLCELLULOSET4V6TWG28DIACT
POLYISOBUTYLENE (1300 MW)241BN7J12YIACT
POLYSORBATE 60CAL22UVI4MIACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT

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
55a3e380-d4b1-3eaa-e063-6294a90a104b438a5d21-4461-84df-e063-6294a90aa66c2026-07-02WarningsExact identifier
spl set id: 438a5d21-4461-84df-e063-6294a90aa66c

Reported adverse events (FAERS/openFDA)#

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