FDA.reportPublic FDA data

Maximum Strength Wart Remover Patches

Manufacturer
Henan Toudaorong Biotechnology Co., Ltd.
Effective date
2025-11-23
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:17:46

Label at a glance#

ProductMaximum Strength Wart Remover Patches
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredient

Salicylic acid 30%
Purpose Wart remove

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.

OTC - PURPOSE SECTION

For the removal of common warts and plantar warts.Common warts arerough, cauliflower-like growths often on fingers/hands. Plantar wartsoccur on the soles of feet.

WARNINGS SECTION

Warnings

Do not use on face, genital warts, moles with hair, or irritated/reddened skin

INACTIVE INGREDIENT SECTION

Inactive ingredients Cellulose Gum, Propylene Glycol, Cyclodextrin, MelaleucaAlternifolia (Tea Tree) Leaf Oil, Centella Asiatica Extract, Polvisobutene.Hvdroxvethylcelulose,Disodium Phosphate, polysorbate 60
0图

INDICATIONS & USAGE SECTION

on irritated skin or any area that is infected or reddened"

on moles, birthmarks, warts with hair growing from them, genital warts, or wartson the face or mucous membranes,

DOSAGE & ADMINISTRATION SECTION

Directions

wash afected areadry area thoroughly apply the patch directly over the wart or tagrepeat this procedure every 48 hours as needed, until the wart or tag is removedf崧or up to 12 weeks"Apply the procedure every 48 hours, up to 12 weeks, until the wart isremoved.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

85136-011-0185136-011-01

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2727377salicylic acid 30 % Medicated PatchPSN1
2727377salicylic acid 0.3 MG/MG Medicated PatchSCD1
2727377salicylic acid 30 % 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
85136-011-01Maximum Strength Wart Remover Patches144 in 1 BOXPATCH1441
85136-011-01Maximum Strength Wart Remover Patches10 mg in 1 PATCHPATCH101

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
85136-01185136-011-01

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
POLYSORBATE 60CAL22UVI4MIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
HYDROXYETHYL CELLULOSE (140 CPS AT 5%)8136Y38GY5IACT
CELLULOSE GUMK679OBS311IACT
SALICYLIC ACIDO414PZ4LPZACTIB
CENTELLA ASIATICA7M867G6T1UIACT
DISODIUM PHOSPHATE22ADO53M6FIACT
CYCLODEXTRIN7E6SK9QDT8IACT
MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OILVIF565UC2GIACT
POLYISOBUTYLENE (1000 MW)5XB3A63Y52IACT

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
44448797-51a9-321e-e063-6394a90ab71344448797-51a8-321e-e063-6394a90ab7132025-11-23WarningsExact identifier
spl id: 44448797-51a9-321e-e063-6394a90ab713
spl set id: 44448797-51a8-321e-e063-6394a90ab713

Reported adverse events (FAERS/openFDA)#

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