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Corn remover pads 40 g/1001 Paste, 42-count — NDC 85056-0002-09 package photo

Corn remover pads 40 g/1001 Paste, 42-count

by Henan Shouerkang Health Industry Co., Ltd · 42 PASTE in 1 BOX (85056-002-09)
NDC 85056-0002-09
🏷️ FDA NDC (as labeled) 85056-002-09 billing pads the product segment with a zero
This package
Contains42-count Pack sizes10 compare ↓
Also comes in: 6 pastes 85056-0002-01 12 pastes 85056-0002-02 18 pastes 85056-0002-03 20 pastes 85056-0002-04 24 pastes 85056-0002-05 30 pastes 85056-0002-06 36 pastes 85056-0002-07 40 pastes 85056-0002-08 60 pastes 85056-0002-10
OTC On market Non-controlled
🗂️ 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

🆔 Identity & classification

FDA NDC (as labeled) 85056-002-09
Product NDC 85056-002
11-digit billing NDC 85056000209
UNII O414PZ4LPZ
Application # 505G(a)(3)
SPL Set ID 2e617119-531d-af7b-e063-6294a90a8ca6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-02-18
Route CUTANEOUS
Dosage form PASTE
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 85056-002-09 — 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 → 85056-0002-09. 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

LabelerHenan Shouerkang Health Industry Co., Ltd
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code85056
First marketedFeb 2025
Product typeHuman Otc Drug
Portfolio3 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 an over-the-counter topical paste containing salicylic acid, marketed as a corn remover. Salicylic acid is a keratolytic agent, meaning it typically functions to soften and break down thickened, hardened skin. This product is applied directly to the skin surface and is classified as an OTC monograph drug, which means it is marketed under established FDA guidelines for its category rather than as an individually approved application.

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 UBL01213LI
    An antioxidant is a chemical substance that prevents oxygen from damaging other ingredients in the medicine during storage. It helps keep the medication stable and effective throughout its shelf life.
  • UNII I9O0E3H2ZE
    Paraffin is a waxy, petroleum-derived substance used as a coating, lubricant, and hardening agent in tablets and capsules. It helps protect the medicine from moisture and gives pills a smooth finish.
  • UNII 4T6H12BN9U
    Petrolatum is a purified mineral oil-based jelly derived from petroleum. In medicines, it acts as an emollient, lubricant, and moisture barrier to soften skin, reduce friction, and help prevent water loss from formulations.
  • UNII 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.

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

The official label also statesVaseline, Antioxidant, Hard paraffin, Titanium dioxide

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 gPer 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.
Try another pack size: 6 pastes 12 pastes 18 pastes 20 pastes 24 pastes 30 pastes 36 pastes 40 pastes 60 pastes
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
Corn remover pads 40 g/1001this 85056-0002-09 Henan 42 pastes — — 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

🏛️
2025
On the market since
Feb 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
85056-0002-01 6 PASTE in 1 BOX (85056-002-01) 2025-02-18 Active
85056-0002-02 12 PASTE in 1 BOX (85056-002-02) 2025-02-18 Active
85056-0002-03 18 PASTE in 1 BOX (85056-002-03) 2025-02-18 Active
85056-0002-04 20 PASTE in 1 BOX (85056-002-04) 2025-02-18 Active
85056-0002-05 24 PASTE in 1 BOX (85056-002-05) 2025-02-18 Active
85056-0002-06 30 PASTE in 1 BOX (85056-002-06) 2025-02-18 Active
85056-0002-07 36 PASTE in 1 BOX (85056-002-07) 2025-02-18 Active
85056-0002-08 40 PASTE in 1 BOX (85056-002-08) 2025-02-18 Active
85056-0002-09 You're viewing this 42 PASTE in 1 BOX (85056-002-09) 2025-02-18 Active
85056-0002-10 60 PASTE in 1 BOX (85056-002-10) 2025-02-18 Active

You're viewing one of 10 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 85056-0002-09?
NDC 85056-0002-09 is a 42-count package — 42 paste in 1 box.
What is the difference between NDC 85056-0002-09 and NDC 85056-0002-01?
Both are Corn remover pads 40 g/1001 Paste — the drug itself is identical. NDC 85056-0002-09 is the 42-count package, while NDC 85056-0002-01 is the 6 pastes package.
What NDC number is used to bill for this package of Corn remover pads 40 g/1001 Paste?
Bill NDC 85056-0002-09 — the 11-digit billing format is 85056000209. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 85056-002-09, 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: 85056-0002-09, written without dashes as 85056000209. 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 85056-0002-09, the first segment (85056) is the labeler code FDA assigned to Henan Shouerkang Health Industry Co., Ltd; the middle segment (0002) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) 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 Henan Shouerkang Health Industry Co., Ltd. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 9 other package presentations of this same product, including 6 pastes (85056-0002-01), 12 pastes (85056-0002-02), 18 pastes (85056-0002-03). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Henan Shouerkang Health Industry 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.

📄 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
🎯 Indications and Usage 8 words ▾

Use Uses:for softening and removing corns and calluses

⏱️ Dosage and Administration 130 words ▾

Directions 1.May soak corn/callus in warm water for 5 minutes to assist in removal before apply the patch. 2.Clean and dry affected area thoroughly, then apply the patch directly to the corn/callus, ensuring the medication core does not touch surrounding healthy skin. If corn/callus is small than medicatied core,remove and trim the core to fit precisely before apply.

For extra protection, apply a thin layer of Vaseline or a similar protective cream around the corn/callus. 3. Secure the patch in place using additional bandage ifnecessary to prevent any movement during wear.

4.Replace the patch with a fresh one every 12 to 24 hours as needed, adhering to the recommended time frame for optimal efficacy. 5.Continue this application regimen until the corn/callus is fully resolved,repeating steps 1 through 4 as necessary.

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 7 words ▾

Other information store between 58°F to 85°F

🧪 Active Ingredient 5 words ▾

Active Ingredient(s) Salicylic acid 40%

🧪 Inactive Ingredients 8 words ▾

Inactive ingredients Vaseline, Antioxidant, Hard paraffin, Titanium dioxide

🎯 Purpose 5 words ▾

Purpose corn and callus remover

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85056-0001-02 · Henan 85056-0003-01 · Henan →
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.