Home › NDC Lookup › Ingredients › Salicylic Acid › 87295-0001-01
🧴image loading
(from DailyMed)

Wart Remover-SALICYLIC ACID 17 g/100mL Liquid — NDC 87295-0001-1 (Billing 87295-0001-01)

by Ecommerce Digital Sales LLC · 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR

This is a package of Wart Remover-SALICYLIC ACID 17 g/100mL Liquid from Ecommerce Digital Sales LLC, no longer marketed (first marketed Feb 2026), no longer in the FDA NDC Directory. It is the main listing for this product, which comes in 2 package sizes.

NDC 87295-0001-01
🏷️ FDA NDC (as labeled) 87295-0001-1 billing pads the package segment with a zero
This package
Contains30 mL in 1 bottle, with applicator Pack sizes2 compare ↓
Main listing for product 87295-0001 · Also comes in: 2 bottles 87295-0001-2
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 2, 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 87295-0001-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87295 labeler · 0001 product · 1 package
Package marketed since
Feb 23, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0860009669307
FDA record last changed
Jul 2, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Jul 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87295-0001-1
Product NDC 87295-0001
11-digit billing NDC 87295000101
RxCUI 312881
UNII O414PZ4LPZ
UPC 0860009669307
Application # M028
SPL Set ID f51666ff-5ee5-4dc9-9b05-b52f54be8a21
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Jul 2026)
Marketing start 2026-02-23
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 312881
Why two NDCs? The FDA registers this code as 87295-0001-1 — a 5-4-1 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 package segment → 87295-0001-01. 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

📗 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: 2 bottles
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
87295-0001-01 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR 2026-02-23 — Discontinued by firm
87295-0001-02 87295-0001-2 2 BOTTLE, WITH APPLICATOR in 1 CARTON / 30 mL in 1 BOTTLE, WITH APPLICATOR 2026-02-23 — Discontinued by firm

Pack size FAQ

What quantity is in this package?
This package is listed by the FDA — 1 bottle, with applicator in 1 carton / 30 ml in 1 bottle, with applicator.
What NDC number is used to bill for this package of Wart Remover-SALICYLIC ACID 17 g/100mL Liquid?
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/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/100mLthis 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 —
GlyCylic 17 g/100mL 49406-0009-15 The 1 bottle — — FDA listed —
Pureskin wart remover 17 g/100mL 87217-0002-01 BENLONG 1 bottle — — 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
Feb 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerEcommerce Digital Sales LLC
FDA applicationM028 (OTC MONOGRAPH DRUG)
Labeler code87295
First marketedFeb 2026
Product typeHuman Otc Drug
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 44 words ▾

USES: For the removal of common warts and plantar warts. The common wart is easily recognized by the rough ''cauliflower-like'' appearance of surface The planter wart is recognized by its location only on the bottom of foot, its tenderness, & interruption of footprint pattern

⏱️ Dosage and Administration 60 words ▾

DIRECTIONS Wash affected area (may soak wart in warm water for 5 minutes) Dry area thoroughly Using the applicator, apply a small amount of the product to sufficiently cover each wart & let it dry Use once or twice daily as needed until wart is removed Wart removal may take upto 12 weeks Children under 2 years: ask a doctor

⚠️ Warnings 5 words ▾

WARNING: For external use only.

🧪 Active Ingredient 4 words ▾

Active Ingredient Salicylic Acid.......17%

🧪 Inactive Ingredients 7 words ▾

INACTIVE INGREDIENT Water, Gycerin, Polyethylene Glycol, Borneol

🎯 Purpose 3 words ▾

PURPOSE: Wart Remover

📄 Do Not Use 40 words ▾

DO NOT USE: On irritated skin or any area that is infected If you are diabetic or have poor blood circulation On birthmarks, moles, warts with hair growing from them, genital warts, warts on face, or warts on mucus membranes

📄 When Using This Product 33 words ▾

WHEN USING THIS PRODUCT: Avoid contact with eyes and mucus membrans if burning,discomfort or irritation occurs, stop use & ask a doctor Cap bottle tightly after use Flammble-keep away from heat and flame

📄 Stop Use and Ask a Doctor If 20 words ▾

STOP USE AND ASK A DOCTOR IF: Discomfort persists Excessive irritation occurs You do not see improvement within 12 weeks

📄 Keep Out of Reach of Children 17 words ▾

KEEP OUT OF REACH OF CHILDREN: If swallowed, get medical help or contact a Poison Control Center

📄 Other Information 33 words ▾

OTHER INFORMATION: Store at 20-25 °C (68-77 °F) Keep cap tightly closed;avoid contact with fabrics surfaces Protect from freezing and excessive heat Tamper evident: do not use if seal is broken or missing

📄 Questions or Comments 3 words ▾

QUESTIONS ? 1-800-534-1894

📄 Package Label / Principal Display Panel 16 words ▾

NDC 87295-0001-1 skin tag remover 1 Pack outlined

NDC 87295-0001-2 skin tag remover 2 Pack outlined

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

Death632
Disabling147
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 18,985 111
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 No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
Inactive ingredients (structured) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 2 bottles (87295-0001-02). 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?
Ecommerce Digital Sales 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.
← 87290-0004-04 · Saltair 87296-0001-01 · Shanghai →
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.