Dr. Luke Bee Venom Wart and Corn Remover

Manufacturer
DANOUS LAND FLOOW LLC
Effective date
2025-12-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:25:53

Label at a glance#

ProductDr. Luke Bee Venom Wart and Corn Remover
Active ingredientSALICYLIC ACID
Label structure2 sections

Label contents#

Full prescribing information#

Drug Facts

INFORMATION FOR PATIENTS SECTION

Drug Facts

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 17%

Purpose

OTC - PURPOSE SECTION

Wart remover

Uses

INDICATIONS & USAGE SECTION

  • for the removal of common warts (easily recognized by the rough “cauliflower-like” surface)
  • for the removal of plantar warts (on the bottom of the foot)

Warnings

WARNINGS SECTION

for external use only

Do not use

OTC - DO NOT USE SECTION

  • on irritated, infected, or reddened skin
  • on moles, birthmarks, warts with hair, or on the face
  • on genital warts, mucous membranes, or on the nose or lips
  • if you have diabetes or poor blood circulation
  • on broken skin
  • if you are allergic to bee stings/bee venom (product contains bee venom as an inactive ingredient)
  • with any other wart removal product
  • on sensitive areas such as the face, armpits, or private areas
Ask a doctor before use if you are

OTC - ASK DOCTOR SECTION

  • pregnant or breastfeeding
  • using any other topical medications on the area
When using this product

OTC - WHEN USING SECTION

  • avoid contact with eyes. If contact occurs, flush with water for 15 minutes.
  • avoid inhaling vapors. Use in a well-ventilated area.
  • transient stinging or mild irritation may occur.
  • do not touch the liquid film until it has completely dried.
Stop use and ask a doctor if

OTC - STOP USE SECTION

  • discomfort, burning, or irritation persists
  • excessive skin irritation occurs
  • the wart does not improve after 12 weeks of use
  • accidental ingestion occurs
Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

  • If swallowed, get medical help or contact a Poison Control Center right away.
  • Not for use on children under 12 years old.

Directions

DOSAGE & ADMINISTRATION SECTION

  1. Soak the wart in warm water for about 15 minutes; dry thoroughly.
  2. Using the precision brush, apply a thin layer to cover the wart. Wait until it dries to a film, then apply an extra thin layer if needed.
  3. Use twice daily. For larger or thicker warts, more frequent application may be used if needed.
  4. After 3 days of continuous use, gently remove the dried film with tweezers, then continue applying.
  5. After several days, you may also remove loosened dead skin after soaking; do not cut the wart.

Other Information

STORAGE AND HANDLING SECTION

  • Store at 20–25°C (68–77°F). Avoid heat and direct sunlight.
  • Keep bottle tightly closed to prevent evaporation.
  • Tamper evident: Do not use if safety seal is broken or missing.
  • Drying time: normally forms a protective film within 20–30 seconds. In humid or rainy weather, drying may take longer.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Bee Venom, Water, Brucea javanica, Coptis chinensis, Phellodendron amurense, Acorus calamus, Menthol, Honeysuckle, Triclosan, Borneol, Glycerin.

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PackagePackage

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codeqrco.de/behIWjpackage_under_1mb.jpg

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
87147-010-01Dr. Luke Bee Venom Wart and Corn Remover30 mL in 1 BOTTLE, WITH APPLICATORSOLUTION301

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87147-01087147-010-01

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
459e8a5a-3e5f-944b-e063-6394a90a90f4459e8a5a-3e5e-944b-e063-6394a90a90f42025-12-10WarningsExact identifier
spl id: 459e8a5a-3e5f-944b-e063-6394a90a90f4
spl set id: 459e8a5a-3e5e-944b-e063-6394a90a90f4

Reported adverse events (FAERS/openFDA)#

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