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Totclear Wart Remover Patches Salicylic Acid 400 mg/g Patch, 144 patches — NDC 87725-0006-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Totclear Wart Remover Patches Salicylic Acid 400 mg/g Patch, 144 patches — NDC 87725-006-01 (Billing 87725-0006-01)

by GOOD BRIDGE LLC · 144 PATCH in 1 BOX / 1 g in 1 PATCH

This is a package of 144 patches of Totclear Wart Remover Patches Salicylic Acid 400 mg/g Patch from GOOD BRIDGE LLC, marketed since Aug 2026 and currently FDA-listed. It is this product's only package size.

NDC 87725-0006-01
🏷️ FDA NDC (as labeled) 87725-006-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Sep 3, 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

NDC database record

One package, one record: these facts belong to NDC 87725-006-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87725 labeler · 006 product · 01 package
Package marketed since
Aug 17, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8772500601 3
FDA record last changed
Sep 3, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87725-006-01
Product NDC 87725-006
11-digit billing NDC 87725000601
RxCUI 240559
UNII O414PZ4LPZ
Application # M028
SPL Set ID ff9fc31d-af19-4a37-8499-624f34fab4be
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-17
Route TOPICAL
Dosage form PATCH
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 240559
Why two NDCs? The FDA registers this code as 87725-006-01 — 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 → 87725-0006-01. 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?

TotClear Wart Remover Patches is an over-the-counter topical patch containing salicylic acid. This product is marketed under FDA's monograph rules for wart removers. Salicylic acid is commonly used in wart removal products because it functions to soften and break down the outer layers of skin where warts form. The patch is applied directly to the skin over the affected area.

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 eachPer 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
87725-0006-01 You're viewing this Main listing 144 PATCH in 1 BOX / 1 g in 1 PATCH 2026-08-17 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Wart Removers 400 mg/g 79481-0620-01 Meijer 18 patches — — FDA listed —
Medicated Corn Removers 400 mg/g 79481-1613-01 Meijer 9 patches — — FDA listed —
Medicated Corn Removers 400 mg/g 55319-0476-09 Family 4 pouches — — FDA listed —
Medicated Callus Removers 400 mg/g 79481-0609-01 Meijer 4 patches — — FDA listed —
Wart Remover 400 mg/g 51316-0757-18 CVS 18 patches — — FDA listed —
Premier Solutions Wart Removers 400 mg/g 56104-0911-01 Premier 18 patches — — FDA listed —
Plantar Wart Remover 400 mg/g 59779-0138-24 CVS 24 patches — — FDA listed —
Gel Corn Remover 400 mg/g 59640-0802-01 HEB 6 patches — — FDA listed —
Corn Removers 400 mg/g 67091-0750-09 WinCo 9 patches — — FDA listed —
Medicated Callus Removers Extra Thick 400 mg/g 79481-0611-01 Meijer 4 patches — — FDA listed —
Medicated Plantar Wart Remover 400 mg/g 79481-0619-01 Meijer 24 patches — — FDA listed —
Medicated Callus Removers 400 mg/g 56104-0913-01 Premier 4 patches — — FDA listed —
Totclear Wart Remover Patches 400 mg/gthis 87725-0006-01 GOOD 144 patches — — 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
Aug 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 7EV65EAW6H
    Lanolin is a waxy substance derived from sheep's wool. It's used in medicines as an emollient and skin-conditioning agent to soften formulations and improve spreadability in topical products like creams and ointments.
  • UNII 89NA02M4RX
    Pectin is a natural fiber extracted from fruit and plants. It's used in medicines as a thickener, binder, and gelling agent to create the right texture and help the product hold together.
  • UNII 88S87KL877
    Rosin is a sticky resin extracted from pine trees. It's used in medicines as a binder and adhesive to help hold tablet ingredients together and improve how the medicine sticks to surfaces.
  • UNII 2ZA36H0S2V
    Beeswax is a natural wax produced by honeybees. In medicines, it works as a coating agent and thickener to control how fast the drug dissolves and improve the product's texture and appearance.
  • UNII SOI2LOH54Z
    Zinc oxide is a white mineral powder used in medicines as a protective barrier agent and color additive. It helps shield skin in topical products and may also serve as a filler or opacifying ingredient.

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

The official label also statesInactive Ingredients: Beeswax Pectin Lanolin Rosin Zinc Oxide

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

LabelerGOOD BRIDGE LLC
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code87725
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from GOOD BRIDGE LLC labeler code 87725

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 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 57 words ▾

Uses: For the removal of common warts. For the removal of plantar warts on the bottom of the foot. 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, it's tenderness, and the intteruption of the footprint pattern.

⏱️ Dosage and Administration 44 words ▾

Direction: Wash the affected area. May soak the wart in warm water for 5 minutes. Dry the area thoroughly. Cut plaster to fit wart. Apply medicated plaster. Reapeat this procedure every 48 hours as needed (until wart is removed) for up to 12 weeks.

⚠️ Warnings 59 words ▾

For external use only. Do not use this product on irritated skin, or any area that is infected or reddened, if you are diabetic, or if you have poor blood circulation. Do not use on moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes. if discomfort persist, see your doctor.

🧪 Active Ingredient 3 words ▾

Salicylic Acid 40%

🧪 Inactive Ingredients 8 words ▾

Inactive Ingredients: Beeswax Pectin Lanolin Rosin Zinc Oxide

🎯 Purpose 2 words ▾

Wart Remover

📄 Do Not Use 49 words ▾

Do not use this product on irritated skin, or any area that is infected or reddened, if you are diabetic, or if you have poor blood circulation. Do not use on moles, birthmarks, warts with hair growing from them, genital warts or warts on the face or mucous membranes.

📄 Stop Use and Ask a Doctor If 6 words ▾

if discomfort persist, see your doctor.

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children.

📄 Other Information 12 words ▾

Other Information: Store at room temperature. Keep out of reach of children.

📄 Questions or Comments 7 words ▾

Questions or comments? Contact us at: [email protected]

📄 Package Label / Principal Display Panel 9 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL TOTCLEAR WART REMOVER PATCHES package

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

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.

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 form printed on the packaging and shown on DailyMed is the one the FDA registered. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero and the dashes are dropped. The Identity section at the top of this page lists each form of this code.
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 GOOD BRIDGE LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
GOOD BRIDGE 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.
← 87725-0005-01 · GOOD 87725-0007-01 · GOOD →
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.