DR.Luke Liquid Wart Remover Mask

Manufacturer
Dr.luke Healthcare LLC
Effective date
2022-12-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:43:37

Label at a glance#

ProductDR.Luke Liquid Wart Remover Mask
Active ingredientSALICYLIC ACID
Label structure13 sections

Indications and uses

To remove warts such as plantar wart, flat wart, common wart and corns,calluses

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 1.0%

USES

INDICATIONS & USAGE SECTION

To remove warts such as plantar wart, flat wart, common wart and corns,calluses

WARNINGS

WARNINGS SECTION

For external use only, don't contact with eyes or swallow.
Children should use it under the supervision of adults.
Keep out of reach of children.
The liquid can get easily volatilized & crystallized, tighten the cap after use.
Avoid long-term contact with air while using.

OTC - WHEN USING SECTION

For external use only, don't contact with eyes or swallow.
Children should use it under the supervision of adults.
Keep out of reach of children.
The liquid can get easily volatilized & crystallized, tighten the cap after use.
Avoid long-term contact with air while using.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

DO NOT USE

OTC - DO NOT USE SECTION

.On damaged skin(cuts, abrasions, eczema, sunburn).
If you are allergic to any of the ingredients in this product.
. If you are pregnant or breastfeeding.

STOP USE AND SEE A DOCTOR IF

OTC - STOP USE SECTION

You become pregnant, or are planning to become pregnant, while using the product.

DIRECTION

DOSAGE & ADMINISTRATION SECTION

1.Wash the corns or warts with warm water
2. Take out the inner plug from the bottle, install the brush into the bottle cap. press the brush tightly; and tighten the cap on the bottle.
3. Dry the skin, then open the cap, dip the liquid with the brush and apply it on the wart or corn, after the liquid dries and forms to be a mask, apply the liquid again. Apply it in the day and night, and twice in each time.
4. Applying it for 2 weeks until the skin recovers to a healthy situation.

NOTICE :

OTHER SAFETY INFORMATION

*If warts or com are big, you should use it for a longer time.
*If swallowed, get medical help or contact a poison control center right away.

OTHER INGREDIENTS

INACTIVE INGREDIENT SECTION

Prunus Mume(sieb.), Sophora flavescens, Crocus Sativus L. Cnidium Monnieri(L) Cuss, Kochia scoparia(L)Schrad, cortex dictamni, Gleditsia sinensis Lam., Borneol, etc.

QUESTIONS?

OTC - QUESTIONS SECTION

drlukehealthcare.com

Email: Info@drlukehealthcare.com

OTC - PURPOSE SECTION

TOPICAL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

83176-001-01 15mL

83176-001-0183176-001-01

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83176-001-012024-11-21C16284748780-11030e365-5225-111a-e063-dadaa90a10e283176-001 DR.Luke Liquid Wart Remover Mask
83176-001-012024-01-30C16284748780-11030e365-5225-111a-e063-dadaa90a10e283176-001 DR.Luke Liquid Wart Remover Mask

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
83176-00183176-001-01

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
27645be9-357b-96ee-e063-6394a90a743af06c76ee-3277-434c-e053-2995a90a6f3c2024-11-20WarningsExact identifier
spl set id: f06c76ee-3277-434c-e053-2995a90a6f3c

Reported adverse events (FAERS/openFDA)#

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