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RoyceDerm Psoriasis Scalp .Shampoo. Salicylic Acid 3% 3 g/100g Shampoo, 250 g — NDC 85424-0030-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

RoyceDerm Psoriasis Scalp .Shampoo. Salicylic Acid 3% 3 g/100g Shampoo, 250 g — NDC 85424-030-01 (Billing 85424-0030-01)

by RoyceDerm LLC · 250 g in 1 CARTON

This is a package of 250 g of RoyceDerm Psoriasis Scalp .Shampoo. Salicylic Acid 3% 3 g/100g Shampoo from RoyceDerm LLC, marketed since Aug 2026 and currently FDA-listed. It is this product's only package size.

NDC 85424-0030-01
🏷️ FDA NDC (as labeled) 85424-030-01 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 Sep 17, 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 85424-030-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85424 labeler · 030 product · 01 package
Package marketed since
Aug 28, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8542403001 8
FDA record last changed
Sep 17, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85424-030-01
Product NDC 85424-030
11-digit billing NDC 85424003001
RxCUI 205023
UNII O414PZ4LPZ
Application # M032
SPL Set ID 5743f813-57f7-f544-e063-6294a90ad3b8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-08-28
Route TOPICAL
Dosage form SHAMPOO
Substance SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 205023
Why two NDCs? The FDA registers this code as 85424-030-01 — 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 → 85424-0030-01. 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

🧪 What is this product?

RoyceDerm Psoriasis Scalp Shampoo is a topical shampoo marketed as an over-the-counter monograph drug containing 3% salicylic acid. Salicylic acid is commonly used in scalp and skin products to help soften and remove buildup of dead skin cells. This shampoo is typically used as a cleansing product for the scalp in people with psoriasis or similar scaling conditions.

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 gPer 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
85424-0030-01 You're viewing this Main listing 250 g in 1 CARTON 2026-08-28 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
RoyceDerm Seborrheic Dermatitis and Psoriasis Treatment cream 3 g/100g 85424-0014-01 RoyceDerm 100 g — — FDA listed —
RoyceDerm Seborrheic Dermatitis and Psoriasis Treatment cream 3 g/100g 85424-0017-01 RoyceDerm 100 g — — FDA listed —
RoyceDerm Psoriasis Scalp .Shampoo. 3 g/100gthis 85424-0030-01 RoyceDerm 250 g — — 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
Aug 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.

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

  • UNII TR046Y3K1G
    A liquid alcohol derived from petroleum or plant sources. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII 2JYC99Q0WZ
    A plant extract from Artemisia argyi, commonly known as mugwort. It may be used as a flavoring agent, fragrance, or traditional botanical ingredient in some formulations.
  • UNII 04W97Z676Y
    A plant-derived natural substance from Bassia scoparia fruit used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping in the tablet or capsule.
  • UNII M89NIB437X
    Borneol is a waxy, plant-derived alcohol obtained from camphor trees or made synthetically. It's used in medicines as a flavoring agent and penetration enhancer to improve how active ingredients are absorbed.
  • UNII SF3LP91341
    A waxy, skin-like lipid that helps form protective barriers in creams and lotions. It's used as an emollient and skin-conditioning agent to improve texture and help the product spread smoothly.
  • UNII 88KCS7120E
    Ceramide 9 is a fatty lipid found naturally in skin. It's used in medicines as an emollient and skin-conditioning agent to help soften and protect the skin barrier in topical formulations.
  • UNII F1X8L2B00J
    A naturally derived fatty substance that helps bind and condition the product's texture. It works as an emollient and skin-conditioning agent in topical formulations, helping maintain moisture and smoothness.
  • UNII V7M2259XJM
    Ceramide NS is a lipid compound derived from natural sources or synthesized chemically. It works as an emollient and skin-conditioning agent that helps soften and smooth the product's texture while improving how it feels on the skin.
  • 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 JK0MS9P8YL
    Cnidium monnieri fruit oil is a plant-derived oil extracted from the fruit of Cnidium monnieri (Chinese motherwort). In medicines, it serves as a fragrance component, skin conditioning agent, or delivery vehicle to improve product stability and absorption.
  • UNII C80684146D
    A foaming agent and thickener derived from coconut oil. It helps create a smooth texture and stable foam in liquid or semi-solid medicines, improving how the product feels and applies.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII G72P70SL42
    A plant extract from echinacea flowers mixed with water. It may be added to medicines as a flavoring agent or to provide plant-derived properties in the formulation.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII A6W0J6UO7Q
    A plant-derived extract from the fruit of the Chinese honey locust tree. It serves as a natural thickener and emulsifier to help blend ingredients and create a smooth, uniform texture in medicines.
  • UNII YHX98F77PB
    Glycol cetearate is a waxy substance made by combining plant-derived fatty alcohols. It works as an emulsifier and thickener in medications, helping blend oil and water-based ingredients together and giving the product a smooth, stable texture.
  • UNII E89I1637KE
    Guar gum is a natural thickener made from guar bean seeds. It's used in medicines as a binder and thickening agent to hold ingredients together and create the right texture and consistency.
  • UNII 930626MWDL
    A plant extract from goji berries used as a natural coloring agent and flavor enhancer in medicines. It may add color and taste while serving as a source of beneficial plant compounds in the formulation.
  • UNII NDT563S5VZ
    A salt derived from the chemical compound EDTA, used as a chelating agent and preservative. It binds to metal ions in the formulation to prevent spoilage and maintain product stability.
  • 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 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 1HIE915O2J
    Reynoutria multiflora root oil is a plant-derived oil obtained from the roots of Japanese knotweed. It's used in medicines as an emollient and skin-conditioning agent to help soften and smooth the product's texture.
  • UNII C61Y66MY4H
    A plant-derived substance from Sauromatum giganteum used as a binder or thickening agent to help hold the medicine together and improve its texture and stability in the formulation.
  • UNII H51N91QNEB
    A plant extract from the smilax glabra vine used in traditional medicine preparations. It may function as a natural flavoring agent, botanical extract, or ingredient to support the product's intended formulation characteristics.
  • UNII 451W47IQ8X
    Sodium chloride is common table salt. It's used in medicines as a buffer to maintain proper pH, as a filler to add bulk, or to adjust the osmotic balance in liquid formulations.
  • UNII BPV390UAP0
    Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
  • UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
  • UNII 7S9328671Z
    A plant extract from stemona tuberosa root used as a natural preservative and antimicrobial agent in some formulations to help prevent spoilage and extend shelf life.
  • 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.

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

The official label also statesWater (Aqua), Sodium Laureth Sulfate,Cocamidopropyl Betaine, Cocamide MEA,Ethylene Glycol Stearate, Phenoxyethanol,Sodium Chloride, Artemisia Argyi Leaf Extract, Polygonum Multiflorum Root Extract, Cnidium Monnieri Fruit Extract,Kochia Scoparia Fruit Extract, Gleditsia Sinensis Pod Extract, Typhonium Giganteum Rhizome Extract, Stemona Tuberosa Root Extract, Smilax Glabra Rhizome Extract, GuarGum, Citric Acid, Ethylhexylglycerin, Menthol,Borneol, Disodium EDTA, Sophora Flavescens Root Extract, Lycium BarbarumFruit Extract, 1,2-Hexanediol, Ceramide AS,Ceramide NS/Ceramide NG, Echinacea Purpurea Extract, Xanthan Gum, Ceramide AP, Ceramide EOP

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

LabelerRoyceDerm LLC
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85424
First marketedAug 2026
Product typeHuman Otc Drug
Portfolio31 products on file

More NDCs from RoyceDerm LLC labeler code 85424

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 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 34 words ▾

for best results use at least twice a week or as directed by a doctor. wet hair thoroughly. massage shampoo into the scalp. lather, leave on hair & scalp for several minutes. rinse thoroughtly.

⏱️ Dosage and Administration 19 words ▾

For the relief of the symptoms of dandruff and psoriasis. Helps prevent recurrence of itching, scaling, flaking, redness, irritation

⚠️ Warnings 64 words ▾

For external use only. Ask a doctor before use if condition covers a large area of the body. When using this product Avoidcontact with eyes. If contact occurs, rinsethe eyes thoroughly with water. Stop use and ask a doctor if condition worsens or does not improve after regular use as directed If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 3 words ▾

Salicylic Acid 3%

🧪 Inactive Ingredients 71 words ▾

Water (Aqua), Sodium Laureth Sulfate,Cocamidopropyl Betaine, Cocamide MEA,Ethylene Glycol Stearate, Phenoxyethanol,Sodium Chloride, Artemisia Argyi Leaf Extract, Polygonum Multiflorum Root Extract, Cnidium Monnieri Fruit Extract,Kochia Scoparia Fruit Extract, Gleditsia Sinensis Pod Extract, Typhonium Giganteum Rhizome Extract, Stemona Tuberosa Root Extract, Smilax Glabra Rhizome Extract, GuarGum, Citric Acid, Ethylhexylglycerin, Menthol,Borneol, Disodium EDTA, Sophora Flavescens Root Extract, Lycium BarbarumFruit Extract, 1,2-Hexanediol, Ceramide AS,Ceramide NS/Ceramide NG, Echinacea Purpurea Extract, Xanthan Gum, Ceramide AP, Ceramide EOP

🎯 Purpose 2 words ▾

Anti-psoriasis Anti-dandruff

📄 Keep Out of Reach of Children 13 words ▾

If swallowed, get medical help or contact a Poison Control Center right away.

📄 Other Information 9 words ▾

Store at room temperature and out of direct sunlight.

📄 Questions or Comments 5 words ▾

Visit www. roycederm.com Tel +1(307)461-0958

📄 Package Label / Principal Display Panel 2 words ▾

package package

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

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 3% — the ingredient across all brands.

Top reported reactions

Erythema1
Middle Insomnia1
Skin Discolouration1
Thermal Burn1

Reporter sex

1 reports
Male · 100%
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 RoyceDerm LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
RoyceDerm 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.
← 85424-0029-01 · RoyceDerm 85424-0031-01 · RoyceDerm →
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.