HomeNDC LookupIngredientsSalicylic Acid › 81507-0006-01
Dermeleve Scalp Psoriasis Treatment Salicylic acid 2 g/100mL Liquid — NDC 81507-0006-01 package photo

Dermeleve Scalp Psoriasis Treatment Salicylic acid 2 g/100mL Liquid

by Advanced Derm Solutions LLC · 1 BOTTLE in 1 BOX (81507-006-01) / 50 mL in 1 BOTTLE
NDC 81507-0006-01
🏷️ FDA NDC (as labeled) 81507-006-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

🆔 Identity & classification

FDA NDC (as labeled) 81507-006-01
Product NDC 81507-006
11-digit billing NDC 81507000601
NCPDP billing unit ML — per mL (volume)
RxCUI 251577
UNII O414PZ4LPZ
Application # M032
SPL Set ID f55da7a8-0a26-4925-bd3b-fade6156116d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-19
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 81507-006-01 — a 5-3-2 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the product segment → 81507-0006-01. Same drug, same package — only the format differs.
Where does this data come from?
Identifiers from the FDA openFDA NDC Directory and Structured Product Labeling; RxCUI from RxNorm (NLM); GPI from Medi-Span; GCN / HIC / AHFS / legend from First Databank.

🏷️ RxNorm drug class

This medicine belongs to the Salicylic acid and derivatives class.

Drug family (ATC) Salicylic acid and derivatives, Other antifungals for topical use, Antiinflammatory agents, non-steroids
Where does this data come from?
Therapeutic classes from RxNorm RxClass (U.S. National Library of Medicine) — Established Pharmacologic Class (FDA), ATC drug family (WHO) and mechanism of action, matched by this product’s RxCUI.

🏭 Manufacturer & labeler

LabelerAdvanced Derm Solutions LLC
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code81507
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio4 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.

🩺 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's designed to treat acne. Salicylic acid helps by loosening and removing dead skin cells that clog pores — the buildup that leads to breakouts. The multi-step system on this lab...
  • What is this salicylic acid product actually supposed to do for my skin?
  • Some mild tingling, stinging, and peeling is actually expected — that's the salicylic acid doing its job by clearing away dead skin cells. But if the burning or peeling feels exces...
  • My skin feels like it's burning and peeling. Is that normal?
📖 Read our full Salicylic Acid Topical guide →
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.

🧪 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 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 3XUS85K0RA
    Butylene glycol is a clear liquid derived from petroleum or plants that acts as a humectant, solvent, and preservative booster in medicines. It helps keep formulations stable, dissolve active ingredients, and maintain moisture in topical products.
  • UNII M4I0D6VV5M
    Calcium chloride is a salt compound that acts as a firming agent and source of calcium ions in medications. It's used in formulations to help maintain tablet structure, improve texture, or serve as a buffering agent.
  • 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 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • 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 33X04XA5AT
    Lactic acid is a naturally occurring organic acid derived from milk or plant sources. It lowers and maintains pH in formulations, helps preserve the product, and can enhance ingredient stability and absorption.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII 6DC9Q167V3
    Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
  • UNII 45P3261C7T
    Sodium carbonate is an alkaline mineral salt commonly used in medications as a buffer to help maintain pH balance and improve stability. It may also function as a disintegrant to help tablets break apart in the digestive system.
  • UNII 55X04QC32I
    A strong alkaline chemical used to adjust and maintain the pH balance of liquid medicines. It helps keep the medicine stable and ensures it stays effective during storage.
  • UNII BDG873AQZL
    Strontium nitrate is an inorganic salt compound. It may be used as a colorant or in specialized pharmaceutical formulations, though it is not commonly found in most medications.
  • 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.

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

The official label also statesAloe Barbadensis Leaf Juice, Butylene Glycol,Calcium Chloride,Caprylyl Glycol,Citric Acid,Glycerin, Lactic Acid,Phenoxyethanol,Polysorbate 80, Propylene Glycol, Sodium Carbonate, Sodium Hydroxide, Strontium Nitrate,Water, Xanthan Gum

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 DailyMedingredient 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.

💲 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
PanOxyl Clarifying Exfoliant 2 g/100mL 00316-0296-04 Crown 118 ml FDA listed
Hero Pore Release Blackhead Clearing 20 mg/mL 10237-0001-00 Church 100 ml FDA listed
Sulfur 8 Anti-Dandruff Braid 20 mg/mL 12022-0021-00 J. 356 ml FDA listed
Sulfur 8 Fresh Anti-Dandruff 20 mg/mL 12022-0028-00 J. 355 ml FDA listed
Kiehls Since 1851 Dermatologist Solutions Truly Targeted Acne Clearing Solution 20 mg/mL 49967-0055-01 L'Oreal 1 bottle FDA listed
Thayers Since 1847 Natural Remedies Double Action Acne Serum 20 mg/mL 49967-0062-01 L'Oreal 1 bottle FDA listed
Thayers Since 1847 Natural Remedies Blemish Clearing Witch Hazel Aloe Vera Formula Toner 20 mg/mL 49967-0523-01 L'Oreal 355 ml FDA listed
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 51150-0995-01 SICOS 1 bottle FDA listed
Dr. Gross AB Acne Daily Breakout 20 mg/mL 51326-0179-01 Topiderm, 1 bottle FDA listed
Clear Proof Blemish Control Toner Acne Medication 2 g/100mL 51531-6743-05 Mary 1 bottle FDA listed
Anti-Everything Face Serum 2 g/100mL 54111-0180-01 Bentley 1 bottle FDA listed
Emuaid 2 g/100mL 55926-0029-01 Speer 30 ml FDA listed
Exuviance Daily Acne Peel 20 mg/mL 58414-0017-02 NeoStrata 1 bottle FDA listed
Atrix Clarifying Toner 20 mg/mL 59088-0444-08 PureTek 118 ml FDA listed
Acne Warrior Clearing Astringent 2 g/100mL 61197-0121-00 Pacifica 236 ml FDA listed
Clenziderm Pore Therapy Acne Treatment 20 mg/mL 62032-0612-04 Obagi 148 ml FDA listed
Acne Oil Control Primer 20 mg/g 62742-4211-02 Allure 1 tube FDA listed
Shea Moisture 2 g/100mL 64942-2355-02 Conopco 1 bottle FDA listed
Jack Black Bump Fix 20 g/1000g 66738-0022-01 Jack 183 g FDA listed
Pharma Clear Spot Treatment 2 g/100mL 67879-0104-51 PHARMAGEL 1 tube FDA listed
AGE Bright Clearing Serum 20 mg/mL 68479-0184-00 Dermalogica, 3 ml FDA listed
Breakout Clearing Booster 2 mg/100mL 68479-0772-00 Dermalogica, 2 ml FDA listed
Breakout Clearing Booster 2 g/100mL 68479-0773-02 Dermalogica, 1 bottle FDA listed
Neutrogena Clear Pore Oil-Eliminating Astringent 20 mg/mL 69968-0028-08 Kenvue 236 ml FDA listed
Clean and Clear Essentials Deep Cleaning Astringent 20 mg/mL 69968-0209-08 Kenvue 240 ml FDA listed
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0521-08 Kenvue 237 ml FDA listed
Clean and Clear Essentials Acne Toner 20 mg/mL 69968-0820-08 Kenvue 240 ml FDA listed
Neutrogena Oil Free Acne Stress Control Triple Action Toner 20 mg/mL 69968-0925-08 Kenvue 236 ml FDA listed
Acne Spot Treatment 20 mg/mL 70060-1505-01 CosMedical 9 ml FDA listed
e.l.f Plz Clarify Facial Oil 2 g/100mL 70412-0401-01 Zhejiang 30 ml FDA listed
Exfo Tonic Acne Treatment 2 g/100mL 70764-0104-51 CONTROL 1 bottle FDA listed
L BRI Pure n Natural Deep Clean Toner 20 mg/mL 71238-0218-00 L'BRI 188 ml FDA listed
Viaderma Clear Acne Treatment 20 mg/mL 71262-0017-15 VIADERMA 1 bottle FDA listed
Detox Drops Acne Toner 2 g/100mL 71499-0523-01 KENDO 1 bottle FDA listed
FHF Day Breakthru 2 g/100g 72788-0142-11 Summer 1 bottle FDA listed
Dr Throwers Oily Skin Facial Astringent 2 g/100g 72839-0611-02 Derma 57 g FDA listed
Pore Refining Toner 2 g/100g 72957-0013-01 Private 195 g FDA listed
Sunday Riley Peacekeeper Acne Treatment Serum 20 mg/mL 73001-0505-01 Sunday 1 pouch FDA listed
Naturium Salicylic Acid Serum 2% 20 mg/mL 76354-0122-01 e.l.f. 1 bottle FDA listed
e.l.f. PLZ Clarify Facial Oil 20 mg/mL 76354-0419-01 e.l.f. 1 bottle FDA listed
The Inkey List 360 Acne Clearing Serum 20 mg/mL 81136-0028-01 Brand 1 bottle FDA listed
Mara Clear Skin Mineral Milk Acne Treatment 20 mg/mL 81461-0002-00 Mara 30 ml FDA listed
Dermeleve Scalp Psoriasis Treatment 2 g/100mLthis 81507-0006-01 Advanced 1 bottle FDA listed
Peach and Lily Peaches Slices Acne Exfoliating toner 20 mg/mL 81515-0501-01 Peach 120 ml FDA listed
Skinlycious Glow Exfoliant 2 g/100mL 81574-0001-01 Skinlycious 28 ml FDA listed
CeraVe Developed with Dermatologists BHA Exfoliating Toner Acne Treatment 20 mg/mL 82046-0291-01 L'Oreal 237 ml FDA listed
Lancome Paris Clarifique BX-Interceptor Topical Acne Clearing Treatment 20 mg/mL 82046-0955-01 LOreal 1 bottle FDA listed
Clarifying Toner 2 g/100mL 83286-0012-01 Drmtlgy, 189 ml FDA listed
Bubble Super Clear Blemish Prevention Serum 20 mg/mL 83509-0001-01 BUBBLE 1 bottle FDA listed
Doing The Work Salicylic Acid Acne Treatment 20 mg/mL 84234-0001-00 Personal 1 bottle FDA listed
Personal Day Doing the Work Daily Exfoliating Treatment 20 mg/mL 84234-0002-00 Personal 1 bottle FDA listed
Perricone MD Acne Relief Gentle Exfoliating Toner Salicylic Acid Acne Treatment 2 g/100mL 84448-0602-18 THG 1 bottle FDA listed
AHA BHA Blemish Control and Exfoliating Serum 2 g/100mL 85439-0101-01 Banuskin, 30 ml FDA listed
PHOFAY Salicylic Acid Acne Treatment Essence 20 mg/mL 87080-0001-00 Hangzhou 1 bottle FDA listed
Home Health Psoriasis Medicated Scalp and Body Wash 2 g/100mL 76020-0300-08 Home 236 ml FDA listed
PAPATUI Acne Fighting Facial Cleanser 2 g/100mL 83850-0210-00 PAPATUI, 237 ml FDA listed
Tula Skincare Keep It Clear Acne Foam Cleanser 2 g/100mL 84126-0237-18 The 1 bottle FDA listed
Stridex XL Face and Body Pads 2 g/100mL 10157-2114-01 Blistex 1 jar FDA listed
Proactiv CLEAR ZONE BODY PADS 2 g/100mL 11410-0056-00 Alchemee, 75 applicators FDA listed
Acne Defense Face Wash 2 g/100mL 61197-0120-00 Pacifica 172 ml FDA listed
Biore Witch Hazel Pore Clarifying Cleanser 2 g/100mL 10596-0188-67 Kao 200 ml FDA listed
Acne Warrior Body Wash 2 g/100mL 61197-0123-34 Pacifica 355 ml FDA listed
Max Complexion Correction Pads 2 g/100mL 54031-0501-22 PETER 60 patches FDA listed
Pharma Clear Acne Treatment 2 g/100mL 67879-0102-51 PHARMAGEL 1 tube FDA listed
YOUR Anti-Acne Body Wash 2 g/100mL 84229-0018-01 Skin 300 ml FDA listed
Quick Action 2 g/100mL 49035-0934-83 Walmart 200 ml FDA listed
Proactiv Acne Body Wash 2 g/100mL 11410-0074-00 Alchemee, 1 tube FDA listed
Stridex Maximum 2 g/100mL 10157-1006-01 Blistex 1 jar 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
Mar 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.

📊 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

52,595 reports
Male · 27%
Female · 73%
Unknown · 0%

Serious outcomes

Hospitalization800
Death632
Disabling147
Reports over time (by year) — tap or hover for the count & year
2020 2022 2024 2026 18,985 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
81507-0006-01 You're viewing this 1 BOTTLE in 1 BOX (81507-006-01) / 50 mL in 1 BOTTLE 2026-03-19 Active

🧭 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 FDA registers it as 81507-006-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 81507-0006-01, written without dashes as 81507000601. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 81507-0006-01, the first segment (81507) is the labeler code FDA assigned to Advanced Derm Solutions LLC; the middle segment (0006) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Advanced Derm Solutions LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Advanced Derm Solutions 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.

📄 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 21 words

Uses • For relief of the symptoms of psoriasis • Controls scalp itch, irritation, redness, flaking, and scaling associated with psoriasis

⏱️ Dosage and Administration 47 words

Directions Use a dropper to apply to the affected areas of the scalp one to four times daily or as directed by a doctor Massage into the scalp and leave on for at least 30 minutes for the best results. If applying after shampooing, towel-dry hair first

⚠️ Warnings 77 words

Warnings For external use only When using this product Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water If condition worsens or does not improve after regular use of this product as directed, consult a doctor. If the condition covers a large area of the body, consult your doctor before using this product. 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 2%

🧪 Inactive Ingredients 24 words

Inactive ingredients Aloe Barbadensis Leaf Juice, Butylene Glycol,Calcium Chloride,Caprylyl Glycol,Citric Acid,Glycerin, Lactic Acid,Phenoxyethanol,Polysorbate 80, Propylene Glycol, Sodium Carbonate, Sodium Hydroxide, Strontium Nitrate,Water, Xanthan Gum

🎯 Purpose 2 words

Purpose Psoriasis

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