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Dr.Johnes Liquid Skin Wart Corn Remover Salicylic Acid 170 mg/mL Solution, 5 mL — NDC 85818-0004-06 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Dr.Johnes Liquid Skin Wart Corn Remover Salicylic Acid 170 mg/mL Solution, 5 mL — NDC 85818-004-06 (Billing 85818-0004-06)

by Dr.Johnes LLC · 5 mL in 1 BOTTLE, GLASS

This is a package of 5 mL of Dr.Johnes Liquid Skin Wart Corn Remover Salicylic Acid 170 mg/mL Solution from Dr.Johnes LLC, marketed since May 2026 and currently FDA-listed.

NDC 85818-0004-06
🏷️ FDA NDC (as labeled) 85818-004-06 billing pads the product segment with a zero
This package
Contains5 mL Pack sizes6 compare ↓
Product page 85818-0004-01 Also comes in: 6 ml 85818-004-05 8 ml 85818-004-04 10 ml 85818-004-03 15 ml 85818-004-02 20 ml 85818-004-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 13, 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 85818-004-06 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85818 labeler · 004 product · 06 package
Package marketed since
May 22, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8581800406 9
FDA record last changed
Aug 13, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85818-004-06
Product NDC 85818-004
11-digit billing NDC 85818000406
RxCUI 312881
UNII O414PZ4LPZ
Application # M028
SPL Set ID f9efe02a-abc9-4a2f-afb0-9d358fc35c91
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-22
Route TOPICAL
Dosage form SOLUTION
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 312881
Why two NDCs? The FDA registers this code as 85818-004-06 — 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 → 85818-0004-06. 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

📖 What it is MedlinePlus · NLM

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 ↗
📗 Our plain-language guide HelloPharmacist
  • It is used in a facial routine for acne-prone and oil-prone skin. The routine includes a cleanser, serum, toner and emulsion. Salicylic acid helps loosen and shed dead skin cells.
  • Use the cleanser morning and evening, and the serum in the morning after cleansing. Use the toner in the evening on dry skin, and the emulsion at night after cleansing. Avoid your...
  • Mild stinging, burning, itching, dryness and extra peeling can happen. If dryness or peeling bothers you, try using the serum or toner every other day. If it gets excessive, stop a...
  • It is best not to. Using another topical acne medication at the same time makes irritation and dryness more likely. If you get irritated, use only one at a time.
📖 Read our full Salicylic Acid Topical guide →

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.
Try another pack size: 6 ml 8 ml 10 ml 15 ml 20 ml
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
85818-0004-01 85818-004-01 Main listing 20 mL in 1 BOTTLE, GLASS 2026-05-22 — Active
85818-0004-02 85818-004-02 15 mL in 1 BOTTLE, GLASS 2026-05-22 — Active
85818-0004-03 85818-004-03 10 mL in 1 BOTTLE, GLASS 2026-05-22 — Active
85818-0004-04 85818-004-04 8 mL in 1 BOTTLE, GLASS 2026-05-22 — Active
85818-0004-05 85818-004-05 6 mL in 1 BOTTLE, GLASS 2026-05-22 — Active
85818-0004-06 You're viewing this 5 mL in 1 BOTTLE, GLASS 2026-05-22 — Active

You're viewing the smallest of 6 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 5 mL — 5 ml in 1 bottle, glass.
How does this package differ from NDC 85818-0004-05?
Both are Dr.Johnes Liquid Skin Wart Corn Remover Salicylic Acid 170 mg/mL Solution — the drug itself is identical. This page's package is the 5 mL one, while NDC 85818-0004-05 is the 6 ml package.
What NDC number is used to bill for this package of Dr.Johnes Liquid Skin Wart Corn Remover Salicylic Acid 170 mg/mL Solution?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Salicylic Acid 17 g/100mL 70000-0332-01 LEADER/ 1 bottle $0.264 — Availability likely —
Salicylic Acid .17 g/9mL 46122-0362-29 AmerisourceBergen 9 ml $0.366 — Availability likely —
Salicylic Acid 17 g/100mL 70000-0329-01 LEADER/ 1 bottle $0.366 — Availability likely —
Salicylic Acid .17 g/g 00363-8217-10 Walgreen 10 g — — FDA listed —
Salicylic Acid .17 g/g 00363-9889-10 Walgreen 10 g — — FDA listed —
Wart Remover 17 g/100mL 10095-0505-06 World 1 bottle — — FDA listed —
VerruStat Wart Remover 170 mg/mL 44577-0020-15 Clinical 1 bottle — — FDA listed —
Maximum Strength Wart Remover with Salicylic Acid 17 mg/100mg 49035-0017-09 Wal-Mart 9000 mg — — FDA listed —
Salicylic Acid .17 g/g 49035-0018-09 Wal-Mart 9 g — — Discontinued —
Salicylic Acid .17 g/9mL 50804-0748-03 Perrigo 9 ml — — FDA listed —
Salicylic Acid .17 g/9.8mL 50804-0749-03 Geiss, 9.8 ml — — FDA listed —
Kingskin 17 g/100mL 55758-0409-15 Pharmadel 1 bottle — — FDA listed —
Kingskin Saca Callos 17 g/100mL 55758-0442-15 Pharmadel 1 bottle — — FDA listed —
Liquid Callus Remover 170 mg/mL 56104-0501-00 Premier 1 bottle — — FDA listed —
Salicylic Acid .17 mg/15mL 59779-0500-09 CVS 9 ml — — Discontinued —
Salicylic Acid .17 g/9.8mL 63868-0298-03 Chain 9.8 ml — — FDA listed —
Liquid Wart Remover 170 mg/mL 67091-0752-09 WinCo 1 bottle — — FDA listed —
El Mata Callos 170 mg/mL 69469-0017-05 Vitamex 15 ml — — FDA listed —
Verruguin Liquid Wart Remover 170 mg/mL 73635-5810-05 Germa 1 bottle — — Discontinued —
Quita Callos Corn and Callus Remover 170 mg/mL 73635-5811-05 Germa 1 bottle — — Discontinued —
Wart Remover Liquid 17 mg/100mg 74458-0119-06 Guangzhou 30 mg — — FDA listed —
Gemachlich ZuHause WART REMOVER 17 g/100mL 76986-0015-01 Guangdong 3 bottles — — FDA listed —
Gemachlich ZuHause WART REMOVER 17 g/100mL 76986-0018-01 Guangdong 3 bottles — — FDA listed —
BLDAXN Liquid WART REMOVER .17 g/mL 76986-0024-01 Guangdong 2 bottles — — FDA listed —
SootheSense Wart Remover Liquid .17 g/mL 76986-0028-01 Guangdong 30 ml — — FDA listed —
Liquid Corn and Callus Remover 170 mg/mL 79481-0612-01 Meijer 1 bottle — — FDA listed —
Liquid Wart Remover 170 mg/mL 79481-0614-01 Meijer 1 bottle — — FDA listed —
Salicylic Acid 170 mg/mL 79903-0286-09 Wal-Mart 9.8 ml — — FDA listed —
Salicylic Acid 170 mg/mL 81522-0727-01 FSA 1 bottle — — FDA listed —
Salicylic Acid 170 mg/mL 81522-0956-01 FSA 1 bottle — — FDA listed —
Salicylic acid 170 mg/mL 82442-0403-01 Target 1 bottle — — FDA listed —
Salicylic Acid 170 mg/mL 83324-0235-13 Chain 1 bottle — — FDA listed —
Salicylic Acid 170 mg/mL 83324-0236-31 Chain 1 bottle — — FDA listed —
Elsophie Wart Corn Remover 17 g/100mL 83818-0021-01 Shenzhen 30 ml — — FDA listed —
Wart Remover 17 g/100mL 84007-0140-01 Medhome 30 ml — — Discontinued —
OSNOIA Wart Remover 17 g/100mL 85150-0006-01 Guangzhou 15 ml — — FDA listed —
uikeaft Wart and Corn Remover 17 g/100mL 85150-0009-01 Guangzhou 15 ml — — FDA listed —
Bighero Liquid Wart Corn Callus Remover 17 g/100mL 85248-0015-01 Jiangxi 30 ml — — FDA listed —
BITANK Liquid WART CORN CALLUS REMOVER 17 g/100mL 85248-0016-01 Jiangxi 30 ml — — FDA listed —
Ojiog Wart Corn Remover 17 g/100mL 85248-0023-01 Jiangxi 30 ml — — FDA listed —
Alveora CORN WART REMOVER 17 g/100mL 85248-0034-01 Jiangxi 30 ml — — FDA listed —
BEIJIXI Liquid WART CORN REMOVER 17 g/100mL 85248-0038-01 Jiangxi 30 ml — — FDA listed —
Cndanting Wart Remover 17 g/100mL 85248-0039-01 Jiangxi 30 ml — — Discontinued —
Decennalia WART CORN REMOVER 17 g/100mL 85248-0041-01 Jiangxi 30 ml — — Discontinued —
Sanuscode Wart Remover 17 g/100mL 85248-0050-01 Jiangxi 30 ml — — FDA listed —
Healmusz Skin Tag Remover 17 g/100mL 85248-0062-01 Jiangxi 15 ml — — FDA listed —
Healmusz Wart Remover 17 g/100mL 85248-0064-01 Jiangxi 30 ml — — FDA listed —
SYLVIRENE Liquid Wart Corn Callus Remover 17 g/100mL 85248-0069-01 Jiangxi 30 ml — — FDA listed —
Reinreude Wart Remover 17 g/100mL 85248-0074-01 Jiangxi 30 ml — — FDA listed —
Codecure Wart Remover 17 g/100mL 85248-0078-01 Jiangxi 4 ml — — FDA listed —
Healsure Wart Moles Remover 17 g/100mL 85248-0080-01 Jiangxi 4 ml — — FDA listed —
RushCure Wart Removal Serum 17 g/100mL 85248-0085-01 Jiangxi 15 ml — — FDA listed —
OURUI ONE WART COMPLETE Care Kit WART REMOVER 17 g/100mL 85248-0087-01 Jiangxi 30 ml — — FDA listed —
PUVIDA WART REMOVAL System 17 g/100mL 85248-0091-01 Jiangxi 2.5 ml — — FDA listed —
PUVIDA Liquid WART CORN REMOVER 17 g/100mL 85248-0092-01 Jiangxi 30 ml — — FDA listed —
Flobow TAG WART REMOVER 17 g/100mL 85248-0097-01 Jiangxi 30 ml — — FDA listed —
SERYNTH Liquid WART CORN REMOVER 17 g/100mL 85248-0102-01 Jiangxi 30 ml — — FDA listed —
DERMFREE WART REMOVAL System 17 g/100mL 85248-0118-01 Jiangxi 2.5 ml — — FDA listed —
DERMFREE Liquid Wart Corn Callus Remover 17 g/100mL 85248-0120-01 Jiangxi 30 ml — — FDA listed —
WELLREME Wart Remover 17 g/100mL 85248-0129-01 Jiangxi 30 ml — — FDA listed —
SERYNTH WART REMOVAL System 17 g/100mL 85248-0134-01 Jiangxi 2.5 ml — — FDA listed —
Anixike Wart Corn Remover Pen 17 g/100mL 85248-0141-01 Jiangxi 4 ml — — FDA listed —
FOLUPIA Liquid WART CORN REMOVER 17 g/100mL 85248-0149-01 Jiangxi 30 ml — — FDA listed —
AmazingLink Liquid WART CORN REMOVER 17 g/100mL 85248-0188-01 Jiangxi 30 ml — — FDA listed —
Medyi Liquid WART CORN REMOVER 17 g/100mL 85248-0207-01 Jiangxi 30 ml — — FDA listed —
Naikeing Tag Wart Remover 17 g/100mL 85248-0233-01 Jiangxi 30 ml — — FDA listed —
Joymeey WART CORN Liquid 17 g/100mL 85248-0235-01 Jiangxi 30 ml — — FDA listed —
TACRUITF 17% Salicylic acid Wart Remover Serum 17 g/100mL 85304-0010-01 Guangzhou 2 bottles — — FDA listed —
BEHATMH 17% Salicylic acid Wart Remover Serum Pen 17 g/100mL 85304-0015-01 Guangzhou 3 bottles — — FDA listed —
Goodnites Wart Remover 17 g/100mL 85578-0001-01 Zhengzhou 1 bottle — — FDA listed —
Goodnites Skin tag and wart remover 17 g/100mL 85578-0006-01 Zhengzhou 30 ml — — FDA listed —
BPLXKUR Wart Remover 17 g/100mL 85578-0008-01 Zhengzhou 1 bottle — — FDA listed —
Drmitsui Wart Remover 17 g/100g 85593-0118-01 Guangzhou 20 g — — Discontinued —
WART CORN Liquid REMOVER Mask .17 g/mL 85779-0004-01 Guangdong 1 bottle — — FDA listed —
BURRRER Wart Remover 17 g/100mL 85795-0001-01 Shenzhen 30 ml — — FDA listed —
CIDUAM Wart Corn Remover 17 g/100mL 85795-0003-01 Shenzhen 30 ml — — FDA listed —
Dr. Johne SKIN TAG REMOVER 170 mg/mL 85818-0001-01 Dr.Johnes 10 ml — — FDA listed —
Dr.Johnes SKIN TAG REMOVER 170 mg/mL 85818-0002-01 Dr.Johnes 10 ml — — FDA listed —
Dr.Johnes Liquid Skin Wart Corn Remover 170 mg/mLthis 85818-0004-06 Dr.Johnes 5 ml — — FDA listed —
Wart Remover 17 g/100mL 85825-0003-01 Shenzhen 30 ml — — Discontinued —
Wart Remover 17 g/100mL 85834-0002-01 Shenzhen 30 ml — — Discontinued —
Skin Tag Wart And Corn Remover 17 g/100g 87096-0001-01 Zhenping 50 g — — FDA listed —
Subleef SKIN WART CORN REMOVER 17 g/100mL 87152-0005-01 Putian 30 ml — — FDA listed —
Wart Remover 17 g/100mL 87255-0003-01 Shenzhen 15 ml — — FDA listed —
Wart Remover-SALICYLIC ACID 17 g/100mL 87295-0001-01 Ecommerce 1 bottle — — Discontinued —
BYT BANGYTONG Salicylic acid wart removal solution 17 g/100mL 87382-0156-01 Shenzhen 30 ml — — FDA listed —
Wartremoverliquid 17 g/100mL 87492-0004-01 Shenzhen 1 bottle — — FDA listed —
Liquid WART CORN REMOVER .17 g/mL 87683-0001-01 Jiangxi 1 bottle — — FDA listed —
TOTCLEAR Wart and Spot Eraser 170 mg/mL 87725-0002-01 GOOD 15 ml — — FDA listed —
Liquid Corn and Callus 170 mg/mL 46122-0838-72 AmerisourceBergen 9.8 ml — — FDA listed —
Totclear Skin Wart Corn Remover 170 mg/mL 87725-0007-01 GOOD 20 ml — — FDA listed —
Tagrid Liquid Skin Wart Corn Remover 17% Salicylic Acid 170 mg/mL 85384-0026-01 Tagrid 30 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
May 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.

🧪 Avoiding an ingredient? See Salicylic Acid Topical inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

  • UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII 76013O881M
    A protein extract from honeybee venom. Used in some medicines as an active immunizing agent to desensitize people to bee stings, rather than as a traditional inactive filler.
  • UNII P0M7O4Y7YD
    A plant extract from calendula flowers, traditionally used in formulations. It typically serves as a botanical ingredient that may provide color, fragrance, or skin-conditioning properties to topical products.
  • UNII 00YIU5438U
    Caprylyl glycol is a clear liquid derived from coconut oil. In medicines, it acts as a humectant to retain moisture, a preservative booster to prevent microbial growth, and a solvent to help dissolve or mix other ingredients.
  • UNII 6810070TYD
    Centella asiatica leaf is a plant extract used in medicines as a skin-conditioning agent and natural ingredient. It may help soften or soothe the product's texture and is included for its traditional botanical properties in topical or oral formulations.
  • UNII QI7G114Y98
    Echinacea purpurea is a dried plant extract from the purple coneflower. It's included in some formulations as a botanical ingredient to support the product's intended benefits, though it serves no structural role like binding or coating.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 834K0WOS5G
    A natural fat extracted from sunflower seeds. It acts as an emulsifier and lubricant in medicines, helping mix ingredients that don't normally blend together and allowing the product to flow smoothly during manufacturing.
  • 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 TI9T76XD44
    A natural flavoring derived from orange fruit peel. It adds orange taste and aroma to the medicine, making it more pleasant to take, while also providing natural color.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 6Y8XYV2NOF
    A waxy substance made by honeybees from plant resins and pollen. In medicines, it acts as a binder and coating agent to hold ingredients together and protect the product.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • UNII 856YO1Z64F
    Turmeric is a natural spice derived from the turmeric plant root. It serves as a colorant in medicines, giving products a yellow or golden appearance, and may also provide mild flavoring.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesInactive Ingredients: Water (Aqua) Aloe Barbadensis Leaf Juice Glycerin Citrus Aurantium Dulcis (Orange) Peel Extract Menthol Propolis Extract Bee Venom Echinacea Purpurea Extract Tea Tree Oil Calendula Officinalis Extract Gotu Kola Extract Turmeric Extract (Curcuma Longa) Caprylyl Glycol Sodium Benzoate Potassium Sorbate Xanthan Gum Lecithin

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

LabelerDr.Johnes LLC
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code85818
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio7 products on file

More NDCs from Dr.Johnes LLC labeler code 85818

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 23 words ▾

Uses: Plantar Warts Common Warts Flat Warts Corns in Big Toes Corns in Heels Corns on Feet Corns on Hands Any Other Spot

⏱️ Dosage and Administration 63 words ▾

Directions: Wash and dry the affected area. Apply a small amount directly to the wart, corn or callus. Allow the liquid to dry and form a protective film. Repeat as directed until removed. For best results, use consistently as part of your daily care routine. The liquid formula dries into a protective film to help keep treatment in place. Use only as directed.

⚠️ Warnings 65 words ▾

For external use only Do not use: Face Genital warts Moles Birthmarks Open wounds Irritated skin Infected skin Mucous membranes Ask a doctor before use if you have diabetes or poor blood circulation. Stop use and ask a doctor if discomfort, burning, redness or irritation occurs. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active ingredient: Salicylic Acid 17%

🧪 Inactive Ingredients 45 words ▾

Inactive Ingredients: Water (Aqua) Aloe Barbadensis Leaf Juice Glycerin Citrus Aurantium Dulcis (Orange) Peel Extract Menthol Propolis Extract Bee Venom Echinacea Purpurea Extract Tea Tree Oil Calendula Officinalis Extract Gotu Kola Extract Turmeric Extract (Curcuma Longa) Caprylyl Glycol Sodium Benzoate Potassium Sorbate Xanthan Gum Lecithin

🎯 Purpose 2 words ▾

Wart Remover

📄 Do Not Use 16 words ▾

Do not use: Face Genital warts Moles Birthmarks Open wounds Irritated skin Infected skin Mucous membranes

📄 When Using This Product 13 words ▾

Ask a doctor before use if you have diabetes or poor blood circulation.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if discomfort, burning, redness or irritation occurs.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📄 Questions or Comments 4 words ▾

Questions or comments? [email protected]

📄 Package Label / Principal Display Panel 28 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL package of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid package of Dr. Johnes® Liquid Skin Wart Corn Remover 17% Salicylic Acid

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.

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

Age at onset

Neonate7
Infant1
Child16
Adolescent30
Adult334
Elderly131

Reporter sex

0 reports

Serious outcomes

Hospitalization799
Disabling147
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 9,183 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.

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 Dr.Johnes LLC. 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 5 other package presentations of this same product, including 6 ml (85818-0004-05), 8 ml (85818-0004-04), 10 ml (85818-0004-03). 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?
Dr.Johnes 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.
← 85818-0002-01 · Dr.Johnes 85818-0005-01 · Dr.Johnes →
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.