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Dr. Luke Bee Venom Wart and Corn Remover salicylic acid topical solution 170 mg/1000mL Solution, 30 mL

by DANOUS LAND FLOOW LLC · 30 mL in 1 BOTTLE, WITH APPLICATOR (87147-010-01)
NDC 87147-0010-01
🏷️ FDA NDC (as labeled) 87147-010-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

🆔 Identity & classification

FDA NDC (as labeled) 87147-010-01
Product NDC 87147-010
11-digit billing NDC 87147001001
UNII O414PZ4LPZ
Application # M028
SPL Set ID 459e8a5a-3e5e-944b-e063-6394a90a90f4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-12-10
Route TOPICAL
Dosage form SOLUTION
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 87147-010-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 87147-0010-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏭 Manufacturer & labeler

LabelerDANOUS LAND FLOOW LLC
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code87147
First marketedDec 2025
Product typeHuman Otc Drug
Portfolio5 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

🩺 Clinical

🧪 What is this product?

This is a topical solution marketed as Dr. Luke Bee Venom Wart and Corn Remover containing salicylic acid as the active ingredient. Salicylic acid is typically used in over-the-counter wart and corn removers to help soften and break down thickened skin. This product is an OTC monograph drug, meaning it is marketed under FDA's established rules for this category of skin-removal products rather than as an individually reviewed application. The solution is applied directly to affected skin areas.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

🧪 Inactive Ingredients / Excipients

Inactive ingredients, also called excipients, are components of the drug product other than the active ingredient. They may include fillers, dyes, coatings, preservatives, flavors, or other formulation ingredients.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Dr. Luke Bee Venom Wart and Corn Remover 170 mg/1000mLthis 87147-0010-01 DANOUS 30 ml — — Discontinued —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

⏳ Availability & generic status

🏛️
2025
On the market since
Dec 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87147-0010-01 You're viewing this 30 mL in 1 BOTTLE, WITH APPLICATOR (87147-010-01) 2025-12-10 Inactivated by FDA

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is available.
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 87147-010-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 87147-0010-01, written without dashes as 87147001001. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 87147-0010-01, the first segment (87147) is the labeler code FDA assigned to DANOUS LAND FLOOW LLC; the middle segment (0010) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Who lists this product with the FDA?
DANOUS LAND FLOOW LLC is the labeler of record for this NDC — the company under whose FDA-assigned code the package is listed. The labeler may be the manufacturer itself or a distributor marketing the product under its own code.
Do I need a prescription for this product?
This NDC is listed with FDA as an over-the-counter product, so it does not require a prescription. Follow the package directions, and ask your pharmacist if you are unsure whether it is right for you.
This page identifies an FDA-listed package (the NDC) and reports public regulatory and pricing data about the listing. It is reference information, not a medical recommendation — talk to your pharmacist or prescriber about your own medication.
Where does this data come from?
Listing facts (marketing category, packager status, marketing dates) from the FDA openFDA NDC Directory; label availability from DailyMed; pricing coverage from CMS NADAC; equivalence scope from the FDA Orange Book.

📄 FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 💬 Information for Patients
🎯 Indications and Usage 26 words ▾

Uses 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)

⏱️ Dosage and Administration 89 words ▾

Directions Soak the wart in warm water for about 15 minutes; dry thoroughly. 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.

Use twice daily. For larger or thicker warts, more frequent application may be used if needed. After 3 days of continuous use, gently remove the dried film with tweezers, then continue applying.

After several days, you may also remove loosened dead skin after soaking; do not cut the wart.

⚠️ Warnings 198 words ▾

Warnings for external use only Do not use 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 pregnant or breastfeeding using any other topical medications on the area When using this product 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 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.

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

📦 Storage and Handling 49 words ▾

Other Information 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.

🧪 Active Ingredient 5 words ▾

Active ingredient Salicylic Acid 17%

🧪 Inactive Ingredients 18 words ▾

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

🎯 Purpose 3 words ▾

Purpose Wart remover

💬 Information for Patients ~2 min read ▾

Drug Facts Drug Facts Active ingredient Salicylic Acid 17% Purpose Wart remover Uses 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 for external use only Do not use 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 pregnant or breastfeeding using any other topical medications on the area When using this product 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 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.

If swallowed, get medical help or contact a Poison Control Center right away. Not for use on children under 12 years old. Directions Soak the wart in warm water for about 15 minutes; dry thoroughly.

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. Use twice daily.

For larger or thicker warts, more frequent application may be used if needed. After 3 days of continuous use, gently remove the dried film with tweezers, then continue applying. After several days, you may also remove loosened dead skin after soaking; do not cut the wart.

Other Information 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 Bee Venom, Water, Brucea javanica, Coptis chinensis, Phellodendron amurense, Acorus calamus, Menthol, Honeysuckle, Triclosan, Borneol, Glycerin. Questions www.drlukehealthcare.com Email [email protected]

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87147-0006-01 · DANOUS 87148-0881-00 · Nimex →
For educational and professional reference only — not medical advice. Pricing reflects published NADAC and CMS ASP (free public data) and may differ from your acquisition cost; always verify before billing or dispensing.