Home › NDC Lookup › Ingredients › Skin Wart Remover Liquid › 85636-0030-01
Skin Wart Remover Liquid 40 g/100mL Liquid, 20 mL — NDC 85636-0030-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Skin Wart Remover Liquid 40 g/100mL Liquid, 20 mL — NDC 85636-030-01 (Billing 85636-0030-01) · Product 85636-030

by Shenzhen Earth Surface Trading Co., Ltd. · 20 mL in 1 BOTTLE (85636-030-01)

NDC 85636-030-01 (billing 85636-0030-01) is a package of 20 mL of Skin Wart Remover Liquid 40 g/100mL Liquid from Shenzhen Earth Surface Trading Co., Ltd., marketed since Apr 2026 and currently FDA-listed. It is the main listing for product NDC 85636-030, its only package size.

NDC 85636-0030-01
🏷️ FDA NDC (as labeled) 85636-030-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85636-030-01
Product NDC 85636-030
11-digit billing NDC 85636003001
RxCUI 2741040
UNII O414PZ4LPZ
Application # M028
SPL Set ID 5888ba63-1948-f6e6-e063-6394a90a0414
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-30
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers for NDC 85636-030-01
  • RxCUI (RxNorm): 2741040
  • 11-digit billing NDC: 85636003001
Why two NDCs? The FDA registers this code as 85636-030-01 — 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 → 85636-0030-01. 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.

Clinical

📖 About the active ingredient: Salicylic Acid MedlinePlus · NLM
General information about the ingredient itself — the description of this specific product follows below.

Topical salicylic acid is used to help clear and prevent pimples and skin blemishes in people who have acne. Topical salicylic acid is also used to treat skin conditions that involve scaling or overgrowth of skin cells such as psoriasis (a skin disease in which red, scaly patches form on some areas of the body), ichthyoses (inborn conditions that cause skin dryness and scaling), dandruff, corns, calluses, and warts on the hands or feet. Topical salicylic acid should not be used to treat genital warts, warts on the face, warts with hair growing from them, warts in the nose or mouth, moles, or b...

Read the full MedlinePlus article ↗
🧪 What is this product?

This is a topical liquid product containing salicylic acid, marketed as an over-the-counter wart remover under FDA's OTC monograph rule. Salicylic acid is a keratolytic agent typically used to soften and break down the thickened skin that makes up warts. The liquid form is applied directly to the skin surface where warts occur. This product type does not require individual FDA approval before marketing, as it follows established guidelines for OTC wart-removal drugs.

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.

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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
85636-0030-01 85636-030-01 You're viewing this Main listing 20 mL in 1 BOTTLE (85636-030-01) Sample 2026-04-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Skin Wart Remover Liquid 40 g/100mL 85636-0020-01 Shenzhen 20 ml — — FDA listed —
Skin Wart Remover Liquid 40 g/100mLthis 85636-0030-01 Shenzhen 20 ml — — FDA listed —
Skin Wart Remover Liquid 40 g/100mL 85636-0034-01 Shenzhen 20 ml — — 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
Apr 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.

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 V1IA3S3CUS
    A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
  • UNII 6OM09RPY36
    A plant extract from hawthorn leaves and flowers used in herbal and dietary supplement formulations. It serves as an active botanical ingredient to support the product's intended herbal benefits rather than as a structural or preservation component.
  • UNII U6PQI719P3
    A plant-derived ingredient from hibiscus bark, used as a natural binder and thickener to help hold tablet or capsule ingredients together and improve the product's texture and consistency.
  • UNII 4465L2WS4Y
    A plant extract from Japanese honeysuckle flowers used as a natural flavoring and fragrance ingredient in medicines. It may also help preserve the product and add pleasant taste or aroma.
  • UNII 2S713A4VP3
    A plant-derived resin from the podophyllum plant root. It acts as a binder and thickening agent to help hold tablet or capsule ingredients together and give the medicine its solid form.
  • 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 80N0P0DD9J
    A plant-derived ingredient from Stellera chamaejasme used in traditional medicine formulations. It may serve as a natural extract or botanical component in the preparation.

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

The official label also statesCnidium monnieri, Podophyllum,Hawthorn, Stellera chamaejasm, Sophora flavescens, Earthy hibiscus bark, Honeysuckle

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.

Manufacturer & labeler

LabelerShenzhen Earth Surface Trading Co., Ltd.
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code85636
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio31 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.

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 49 words ▾

Uses Uses · for the removal of common and plantar warts · the common wart is easily recognized by the rough”cauliflower-like” appearance of the surface · 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 6 words ▾

DOSAGE &ADMINISTRATION SECTION DOSAGE &ADMINISTRATION SECTION

⚠️ Warnings 16 words ▾

Warnings For external use only. keep away from fire and flame. only use on affected area.

🧪 Active Ingredient 5 words ▾

ACTIVE INGREDIENT Salicylic acid 40%

🧪 Inactive Ingredients 13 words ▾

Inactive ingredients Cnidium monnieri, Podophyllum,Hawthorn, Stellera chamaejasm, Sophora flavescens, Earthy hibiscus bark, Honeysuckle

🎯 Purpose 3 words ▾

Purpose wart remover

📋 Description 70 words ▾

Directions Of Safe Use: ● wash the affected area ● may soak the tag in warm water for 5 minutes ● dry area thoroughly ● using the applicator(brush swab), apply one drop at a time to sufficiently cover each tag ● allow it to fully absorb a nd let dry ● repeat this procedure once or twice daily as needed (until the tag falling off) for up to 12 weeks

📄 Ask a Doctor Before Use If 35 words ▾

Stop use and ask a doctor: · if discomfort persists.·if you have diabetes or poor blood circulation.Keep out of reach of children. lf swallowed, get medical help or contact a Poison Control Center right away.

📄 When Using This Product 43 words ▾

When using this product : · avoid contact with eyes. If the product gets into the eye,flush with water for 15 minutes · avoid inhaling vapors · cap the bottle tightly ·out of direct sunlight and store at room temperature away from heat

📄 Keep Out of Reach of Children 12 words ▾

Keep Out Of Reach Of Children Keep Out Of Reach Of Children

📄 Package Label / Principal Display Panel 4 words ▾

label PACKAGE LABEL label01

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 85636-030-01, 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: 85636-0030-01, written without dashes as 85636003001. 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 85636-0030-01, the first segment (85636) is the labeler code FDA assigned to Shenzhen Earth Surface Trading Co., Ltd.; the middle segment (0030) 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 Shenzhen Earth Surface Trading Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Shenzhen Earth Surface Trading Co., Ltd. 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.
← 85636-0029-01 · Shenzhen 85636-0031-01 · Shenzhen →
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.