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VerruStat Wart Remover SALICYLIC ACID 170 mg/mL Liquid — NDC 44577-0020-15 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

VerruStat Wart Remover SALICYLIC ACID 170 mg/mL Liquid — NDC 44577-020-15 (Billing 44577-0020-15)

by Clinical Therapeutic Solutions · 1 BOTTLE, WITH APPLICATOR in 1 BOX / 15 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of VerruStat Wart Remover SALICYLIC ACID 170 mg/mL Liquid from Clinical Therapeutic Solutions, marketed since Oct 2013 and currently FDA-listed. It is this product's only package size.

NDC 44577-0020-15
🏷️ FDA NDC (as labeled) 44577-020-15 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed 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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 44577-020-15
Product NDC 44577-020
11-digit billing NDC 44577002015
RxCUI 312881, 1439918
UNII O414PZ4LPZ
Application # M028
SPL Set ID 16607d6e-6a5f-4b03-b38c-3610aef9b165
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-10-16
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 312881
Why two NDCs? The FDA registers this code as 44577-020-15 — 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 → 44577-0020-15. 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.
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
44577-0020-15 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 BOX / 15 mL in 1 BOTTLE, WITH APPLICATOR 2017-02-06 — Active

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/mLthis 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/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

🏛️
2013
On the market since
Oct 2013
📍
2026
Currently FDA-listed
13 years 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.

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

  • 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 464P5N1905
    Butyl acetate is a clear liquid solvent derived from acetic acid and butanol. In medications, it's used primarily in coatings and varnishes to help dissolve and apply protective or delayed-release layers on tablets and capsules.
  • UNII 9H4PO4Z4FT
    A sulfur-containing organic compound used as a solvent and penetration enhancer in medicines. It helps dissolve active ingredients and improve their absorption through skin or mucous membranes.
  • UNII 76845O8NMZ
    Ethyl acetate is a clear, colorless liquid solvent derived from acetic acid and ethanol. In medicines, it dissolves active ingredients, carries them into the product formulation, and helps control how quickly the drug releases and works in your body.
  • UNII ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII KYR8BR2X6O
    Pyroxylin is a cellulose derivative made by treating plant fibers with nitric acid. It serves as a film-former and binder in medications, helping create coatings on tablets and capsules or holding ingredients together in solid dosage forms.
  • UNII 1D1K0N0VVC
    A fat-soluble form of vitamin A used as a colorant and nutritional fortification ingredient. It gives products a yellow or orange tint and increases vitamin A content in the formula.

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

The official label also statesButyl Acetate, Ethyl Acetate, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Nitrocellulose, Retinyl Palmitate, SD-Alcohol 40B

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

LabelerClinical Therapeutic Solutions
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code44577
First marketedOct 2013
Product typeHuman Otc Drug
Portfolio9 products on file
The labeler markets the product; the application holder owns the FDA approval. They’re often the same company but can differ (e.g. a repackager or an authorized generic). A mailing address / phone appears here when the manufacturer includes it in the product’s FDA label (not all do).
Where does this data come from?
Labeler, application holder and registered establishment from the FDA openFDA NDC Directory and Drugs@FDA; address/contact from the product’s FDA label.

FDA label — Drug Facts FDA SPL

The complete FDA label for this product — the official Drug Facts labeling, verbatim, section by section. Jump with a chip, search within the label, or expand everything.
🎯 Indications and Usage ⏱️ Dosage and Administration ⚠️ Warnings 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 33 words ▾

Uses: For the removal of common and plantar warts. The common wart has a rough 'cauliflower-like' appearance. The plantar wart exists only on the bottom of the foot and interrupts the footprint pattern.

⏱️ Dosage and Administration 40 words ▾

Directions wash or soak the affected area and dry thoroughly apply wart remover liquid, with enclosed applicator reapply subsequent applications over existing application repeat the procedure once or twice daily, until wart is completely removed, for up to 12 weeks

⚠️ Warnings 94 words ▾

Warnings For external use only. Do not use this product on irritated skin, on any area that is infected or reddened, if you are a diabetic, or if you have poor blood circulation. If discomfort persists, see your doctor.

Do not use on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes. Flammable. Keep away from fire or flame.

Cap bottle tightly and store at room temperature away from heat. If product gets into the eye, flush with water for 15 minutes. Avoid inhaling vapors.

📦 Storage and Handling 16 words ▾

Other Information Store between 20 degrees to 30 degrees C (68 degrees to 86 degrees F)

🧪 Active Ingredient 5 words ▾

Active Ingredient Salicylic Acid 17%

🧪 Inactive Ingredients 15 words ▾

Other Ingredients Butyl Acetate, Ethyl Acetate, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Nitrocellulose, Retinyl Palmitate, SD-Alcohol 40B

🎯 Purpose 3 words ▾

Purpose wart treatment

📄 Package Label / Principal Display Panel 8 words ▾

VerruStat Liquid Wart Remover 15ml (44577-020-15) VerruStatLiquidBottle VerruStatLiquidBox

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

Reporter sex

52,595 reports

Serious outcomes

Hospitalization800
Life-threatening214
Disabling147
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 1,272 111
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 Clinical Therapeutic Solutions. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Clinical Therapeutic Solutions 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.
← 44577-0002-01 · Clinical 44577-0128-00 · Clinical →
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.