DR.Luke Liquid Wart Remover Mask

Manufacturer
Shandong Yuyaotang Pharmaceutical Co., Ltd
Effective date
2024-09-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 00:22:15

Label at a glance#

ProductDR.Luke Liquid Wart Remover Mask
Active ingredientSALICYLIC ACID
Label structure12 sections

Dosage and administration

1. Wash the area affected by corns or warts with warm water. 2. Remove the inner plug from the bottle. Install the brush into the bottle cap, press the brush tightly, and securely tighten the cap on the bottle. 3. Apply the solution directly to the wart, corn, or callus. Use for an extended period if the wart or corn is large.

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 17%

Purpose

OTC - PURPOSE SECTION

Topical (Wart remover)

Use

INDICATIONS & USAGE SECTION

For the removal of warts, including plantar warts, flat warts, common
warts, corns, and calluses.

Warnings

WARNINGS SECTION

For external use only.

Do not use

OTC - DO NOT USE SECTION

On damaged skin, including cuts, abrasions, eczema, or sunburn.
If allergic to any of the ingredients in this product.
If you are pregnant or breastfeeding, unless directed by a doctor.
Avoid contact with eyes. If contact occurs, flush thoroughly with water.

When Using

OTC - WHEN USING SECTION

Do not swallow.
Children should use this product only under adult supervision.
Avoid prolonged exposure to air while using, as the liquid can easily
volatilize and crystallize.
Tighten the cap after each use. If seal is broken or missing.

Stop Use

OTC - STOP USE SECTION

You become pregnant or are planning to become pregnant while using this product.
Irritation or redness occurs.
Condition worsens or does not improve after regular use.
Keep out of reach of children:
If swallowed, get medical help or contact a Poison Control Center right away.

Keep Oot Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Oot Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

1. Wash the area affected by corns or warts with warm water.
2. Remove the inner plug from the bottle. Install the brush into the
bottle cap, press the brush tightly, and securely tighten the cap on the
bottle.
3. Apply the solution directly to the wart, corn, or callus.
Use for an extended period if the wart or corn is large.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Water, Brucea javanica, Coptis Chinensis, Phellodendron Amurense, Acorus Gramineus, Menthol, Lonicera Japonica, Triclosan, Borneol, Glycerin

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
312881salicylic acid 17 % Topical SolutionPSN1
312881salicylic acid 170 MG/ML Topical SolutionSCD1
312881salicylic acid 17 % Topical SolutionSY1

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
84746-004-01DR.Luke Liquid Wart Remover Mask15 mL in 1 BOTTLELIQUID151

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
84746-004DR.LUKE LIQUID WART REMOVER MASK (LIQUID WART REMOVER MASK) LIQUID [SHANDONG YUYAOTANG PHARMACEUTICAL CO., LTD]11 package rows20240930_231956dc-d0e8-8eb8-e063-6394a90a6cd7.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84746-00484746-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
231956dc-d0e9-8eb8-e063-6394a90a6cd7231956dc-d0e8-8eb8-e063-6394a90a6cd72024-09-27WarningsExact identifier
spl id: 231956dc-d0e9-8eb8-e063-6394a90a6cd7
spl set id: 231956dc-d0e8-8eb8-e063-6394a90a6cd7

Reported adverse events (FAERS/openFDA)#

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