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Dr.Johnes SKIN TAG REMOVER Salicylic Acid 170 mg/mL Solution, 9 mL — NDC 85818-0002-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Dr.Johnes SKIN TAG REMOVER Salicylic Acid 170 mg/mL Solution, 9 mL — NDC 85818-002-02 (Billing 85818-0002-02)

by Dr.Johnes LLC · 9 mL in 1 TUBE

This is a package of 9 mL of Dr.Johnes SKIN TAG REMOVER Salicylic Acid 170 mg/mL Solution from Dr.Johnes LLC, marketed since Jun 2025 and currently FDA-listed.

NDC 85818-0002-02
🏷️ FDA NDC (as labeled) 85818-002-02 billing pads the product segment with a zero
This package
Contains9 mL Pack sizes4 compare ↓
Product page 85818-0002-01 Also comes in: 7 ml 85818-002-04 8 ml 85818-002-03 10 ml 85818-002-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

NDC database record

One package, one record: these facts belong to NDC 85818-002-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85818 labeler · 002 product · 02 package
Package marketed since
Jun 2, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8581800202 7
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85818-002-02
Product NDC 85818-002
11-digit billing NDC 85818000202
RxCUI 312881
UNII O414PZ4LPZ
Application # M016
SPL Set ID b731c55e-31ee-429f-8432-fac7c5718d83
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-02
Route TOPICAL
Dosage form SOLUTION
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 312881
Why two NDCs? The FDA registers this code as 85818-002-02 — 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 → 85818-0002-02. 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: 7 ml 8 ml 10 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
85818-0002-01 85818-002-01 Main listing 10 mL in 1 TUBE 2025-06-02 — Active
85818-0002-02 You're viewing this 9 mL in 1 TUBE 2025-06-02 — Active
85818-0002-03 85818-002-03 8 mL in 1 TUBE 2025-06-02 — Active
85818-0002-04 85818-002-04 7 mL in 1 TUBE 2025-06-02 — Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 9 mL — 9 ml in 1 tube.
How does this package differ from NDC 85818-0002-04?
Both are Dr.Johnes SKIN TAG REMOVER Salicylic Acid 170 mg/mL Solution — the drug itself is identical. This page's package is the 9 mL one, while NDC 85818-0002-04 is the 7 ml package.
What NDC number is used to bill for this package of Dr.Johnes SKIN TAG 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/mLthis 85818-0002-02 Dr.Johnes 9 ml — — FDA listed —
Dr.Johnes Liquid Skin Wart Corn Remover 170 mg/mL 85818-0004-01 Dr.Johnes 20 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

🏛️
2025
On the market since
Jun 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.

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 Z60N6Q6E19
    A plant extract from sweet flag root used in traditional medicine formulations. It may serve as a flavoring agent, fragrance component, or natural additive in herbal preparations.
  • 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 CXS4LJR7EL
    Coptis chinensis root is a plant extract used as a natural flavoring and preservative agent in some medicines. It may help preserve product stability and add a bitter taste component to the formulation.
  • 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 2866QMZ434
    A plant extract from the bark of the Phellodendron chinensis tree. It's used in formulations for its potential to help preserve the medicine and support stability.
  • 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.

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

The official label also statesInactive ingredients: Menthol Coptis chinensis extract (COPTIS CHINENSIS ROOT) Phellodendron extract (PHELLODENDRON CHINENSIS BARK) Acorus gramineus extract (ACORUS GRAMINEUS ROOT) Ethanol (ALCOHOL) Water (WATER)

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 applicationM016 (OTC MONOGRAPH DRUG)
Labeler code85818
First marketedJun 2025
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 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 9 words ▾

Uses For the removal of common warts corns calluses

⏱️ Dosage and Administration 24 words ▾

Directions: Clean and dry the affected area Apply a thin layer once or twice daily Do not apply to open wounds or infected skin

⚠️ Warnings 59 words ▾

For external use only Do not use: on mucous membranes, or broken skin Do not apply to open wounds or infected skin When using this product Avoid contact with eyes Stop use and ask a doctor if excessive 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 24 words ▾

Inactive ingredients: Menthol Coptis chinensis extract (COPTIS CHINENSIS ROOT) Phellodendron extract (PHELLODENDRON CHINENSIS BARK) Acorus gramineus extract (ACORUS GRAMINEUS ROOT) Ethanol (ALCOHOL) Water (WATER)

🎯 Purpose 7 words ▾

Skin Tag, Wart, corn, and callus remover

📄 Do Not Use 18 words ▾

Do not use: on mucous membranes, or broken skin Do not apply to open wounds or infected skin

📄 When Using This Product 8 words ▾

When using this product Avoid contact with eyes

📄 Stop Use and Ask a Doctor If 10 words ▾

Stop use and ask a doctor if excessive 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.

📄 Other Information 11 words ▾

Other information: Store at room temperature Avoid heat and direct sunlight

📄 Questions or Comments 4 words ▾

Questions or comments? [email protected]

📄 Package Label / Principal Display Panel 37 words ▾

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Available in 7 mL, 8 mL, 9 mL, and 10 mL tubes. All packages look the same externally, with the only variation being fill volume. package1 of 10 ml package2 of 10 ml

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 Dr.Johnes SKIN TAG REMOVER (this brand).

Top reported reactions

Vomiting216
Pruritus205
Weight Decreased188
Condition Aggravated184
Urticaria184
Weight Increased183
Hypertension181

Reporter sex

1,853 reports

Serious outcomes

Hospitalization623
Death611
Life-threatening174
Disabling124
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 252 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 3 other package presentations of this same product, including 7 ml (85818-0002-04), 8 ml (85818-0002-03), 10 ml (85818-0002-01). 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.
← 85818-0001-01 · Dr.Johnes 85818-0004-01 · 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.