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DrAny WART REMOVER Salicylic Acid 17 g/100g Liquid, 30 g — NDC 87865-0002-01 package photo

DrAny WART REMOVER Salicylic Acid 17 g/100g Liquid, 30 g

by Hong Kong Juxin Negosyo Kag Komersyo Co., Limited · 30 g in 1 BOTTLE, GLASS (87865-002-01)
NDC 87865-0002-01
🏷️ FDA NDC (as labeled) 87865-002-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Sep 17, 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

🆔 Identity & classification

FDA NDC (as labeled) 87865-002-01
Product NDC 87865-002
11-digit billing NDC 87865000201
RxCUI 312881
UNII O414PZ4LPZ
UPC 6979919520098
Application # M028
SPL Set ID 5a6b7878-060a-d528-e063-6394a90a4215
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-01
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 87865-002-01 — 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 → 87865-0002-01. 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.

🏷️ RxNorm drug class

This medicine belongs to the Salicylic acid and derivatives class.

Drug family (ATC) Salicylic acid and derivatives, Other antifungals for topical use, Antiinflammatory agents, non-steroids
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerHong Kong Juxin Negosyo Kag Komersyo Co., Limited
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code87865
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio2 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?

DrAny Wart Remover is a topical liquid containing 17% salicylic acid, marketed as an over-the-counter monograph drug. Salicylic acid is commonly used in wart-removal products to help soften and break down the layers of skin that make up a wart. This product is applied directly to the affected area on the skin.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • UNII M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • UNII 50268139XV
    A plant-derived ingredient from the fruit of Brucea javanica, a tropical tree. It is used as a flavoring or functional additive in some formulations.
  • UNII 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII 4B51SRR959
    A plant extract from cyperus rotundus (nutgrass) tubers used in traditional medicine formulations. It may function as a natural flavoring agent, preservative, or botanical filler in herbal or botanical drug products.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII R1R8QUL21Z
    A plant-derived ingredient from the woad leaf used in traditional herbal preparations. It may function as a coloring agent, flavoring component, or botanical extract in formulations.
  • UNII 8S10GFI6DX
    A plant-derived ingredient from the roots of Isatis tinctoria, also called dyer's woad. It functions as a natural colorant and may help preserve the product's stability.
  • UNII 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII 1F3X9DRV9X
    Laurocapram is a synthetic oily liquid used as a penetration enhancer and solvent in topical medicines. It helps active ingredients absorb better through the skin and improves how the medication spreads across the application area.
  • UNII 9I70D8O47I
    A plant-derived ingredient from the root of Lithospermum erythrorhizon. It may be used as a natural colorant or preservative in formulations.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • UNII KYR8BR2X6O
    Pyroxylin is a cellulose derivative made by treating plant fibers with nitric acid. It serves as a film-former and binder in medications, helping create coatings on tablets and capsules or holding ingredients together in solid dosage forms.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 9M20DT7Y5D
    A plant-derived ingredient from the roots of Phryma leptostachya. It may function as a natural flavoring, fragrance component, or botanical extract in formulations.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
  • UNII 8W8T17847W
    A nitrogen-containing chemical compound used in pharmaceuticals as a humectant to retain moisture, and sometimes as a keratolytic agent in topical formulations to help soften and remove dead skin cells.

19 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesInactive ingredients ALCOHOL, PROPYLENE GLYCOL, BUTYLENE GLYCOL, UREA, LACTIC ACID,NITROCELLULOSE, ISATIS TINCTORIA LEAF, SOPHORA FLAVESCENS ROOT, PHRYMA LEPTOSTACHYA ROOT, BRUCEA JAVANICA FRUIT, LAUROCAPRAM, LITHOSPERMUM ERYTHRORHIZON ROOT, ISATIS TINCTORIA ROOT, CYPERUS ROTUNDUS TUBER, PHENOXYETHANOL, BISABOLOL, ETHYLHEXYLGLYCERIN, BORNEOL, MENTHOL

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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
Drmitsui Wart Remover 17 g/100g 85593-0118-01 Guangzhou 20 g — — Discontinued —
Wart Remover 17 g/100g 87298-0053-01 Guangzhou 30 g — — FDA listed —
Wart Remover 17 g/100g 87325-0098-01 Yantai 30 g — — FDA listed —
Wart Remover 17 g/100g 87298-0054-01 Guangzhou 30 g — — FDA listed —
DrAny WART REMOVER 17 g/100gthis 87865-0002-01 Hong 30 g — — FDA listed —
Wart Remover 17 g/100g 87298-0056-01 Guangzhou 30 g — — FDA listed —
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

🏛️
2026
On the market since
Sep 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

📊 Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Salicylic Acid (matched by generic name) — the program that covers self-administered drugs. 2 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Salicylic Acid. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$11.2K
Claims incl. refills
43
Beneficiaries
35
Spend / beneficiary
$319.01
Spend / claim
$259.66
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

🔬 Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Salicylic Acid — the ingredient across all brands.

Top reported reactions

Dry Skin12,766
Erythema12,318
Acne11,763
Skin Burning Sensation11,557
Skin Irritation7,730
Skin Exfoliation5,759
Rash4,766

Reporter sex

52,595 reports

Serious outcomes

Death632
Life-threatening214
Disabling147
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 18,985 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
87865-0002-01 You're viewing this 30 g in 1 BOTTLE, GLASS (87865-002-01) 2026-09-01 Active

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
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 ✓ Available
Inactive ingredients (structured) ✓ 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.
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 87865-002-01, 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: 87865-0002-01, written without dashes as 87865000201. 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 87865-0002-01, the first segment (87865) is the labeler code FDA assigned to Hong Kong Juxin Negosyo Kag Komersyo Co., Limited; the middle segment (0002) 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.
Is this package still being marketed?
Yes, per the latest FDA NDC Directory data on this page: this package is listed as actively marketed, with no marketing end date reported by Hong Kong Juxin Negosyo Kag Komersyo Co., Limited. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Hong Kong Juxin Negosyo Kag Komersyo Co., Limited 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📋 Description
🎯 Indications and Usage 62 words ▾

Uses Uses ● for the removal of common warts ● the common wart is easily recognized by the rough “cauliflower-like” appearance of the surface ● for the removal of plantar warts on the bottom of the foot ● the plantar wart is recognized by its location only on the bottom of the foot, its tenderness, and the interruption of the footprint pattern

⏱️ Dosage and Administration 57 words ▾

Directions Directions ● wash affected area ● may soak wart in warm water for 5 minutes ● dry area thoroughly ● apply a small amount at a time with applicator to sufficiently cover each wart ● let dry ● repeat this procedure once or twice daily as needed until wart is removed for up to 12 weeks

⚠️ Warnings 83 words ▾

Warnings Warnings For external use only. Flammable: Keep away from fire or flame. Do not use ● on irritated skin or on any area that is infected or reddened ● if you have diabetes or poor blood circulation ● on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes When using this product ● avoid contact with eyes. If product gets into the eye, flush with water for 15 minutes ● avoid inhaling vapors

🧪 Active Ingredient 5 words ▾

Active Ingredient Salicylic Acid 17%

🧪 Inactive Ingredients 39 words ▾

Inactive Ingredients Inactive ingredients ALCOHOL, PROPYLENE GLYCOL, BUTYLENE GLYCOL, UREA, LACTIC ACID,NITROCELLULOSE, ISATIS TINCTORIA LEAF, SOPHORA FLAVESCENS ROOT, PHRYMA LEPTOSTACHYA ROOT, BRUCEA JAVANICA FRUIT, LAUROCAPRAM, LITHOSPERMUM ERYTHRORHIZON ROOT, ISATIS TINCTORIA ROOT, CYPERUS ROTUNDUS TUBER, PHENOXYETHANOL, BISABOLOL, ETHYLHEXYLGLYCERIN, BORNEOL, MENTHOL

🎯 Purpose 3 words ▾

Purpose Wart Remover

📋 Description 57 words ▾

Easy to use For Common and Plantar Warts Manufacturer: Nanyang Bangtai Biotechnology Co., Ltd. Address: No. 98, Zhangying Village, Huishuwan Street, Pushan Town, Wolong District, Nanyang City, Henan Province Manufactured for: HONG KONG JUXIN NEGOSYO KAG KOMERSYO CO., LIMITED Address: Rm 251 3/F JOIN-IN HANG SING CTR 2-16 KWAI FUNG CRESCENT Kwai Chung, New Territories Hong Kong

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87865-0001-01 · Hong 87866-0001-01 · Yangzhou →
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.