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ProBliva Folliculitis .shampoo. SeleniumDisulfide 1% 6 g/300g; 3 g/300g Shampoo, 300 g — NDC 85464-0006-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ProBliva Folliculitis .shampoo. SeleniumDisulfide 1% 6 g/300g; 3 g/300g Shampoo, 300 g — NDC 85464-006-01 (Billing 85464-0006-01)

by CAVTECH HOLDING LLC · 300 g in 1 CARTON

This is a package of 300 g of ProBliva Folliculitis .shampoo. SeleniumDisulfide 1% 6 g/300g; 3 g/300g Shampoo from CAVTECH HOLDING LLC, marketed since May 2026 and currently FDA-listed. It is this product's only package size.

NDC 85464-0006-01
🏷️ FDA NDC (as labeled) 85464-006-01 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 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) 85464-006-01
Product NDC 85464-006
11-digit billing NDC 85464000601
RxCUI 2743372
UNII O414PZ4LPZ, Z69D9E381Q
Application # M032
SPL Set ID 502caa29-f817-cc12-e063-6394a90a2240
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-05-15
Route TOPICAL
Dosage form SHAMPOO
Substance SALICYLIC ACID; SELENIUM SULFIDE
Quick answers
  • RxCUI (RxNorm): 2743372
Why two NDCs? The FDA registers this code as 85464-006-01 — 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 → 85464-0006-01. 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 Other antifungals for topical use class.

Drug family (ATC) Other antifungals for topical use
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?

ProBliva Folliculitis is a topical shampoo containing salicylic acid and selenium sulfide. Salicylic acid is commonly used in shampoos to help exfoliate and remove buildup from the scalp and hair. Selenium sulfide is typically included in shampoos to address fungal and bacterial scalp concerns. This is an over-the-counter monograph drug, meaning it is marketed under established FDA guidelines for its product category.

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
85464-0006-01 You're viewing this Main listing 300 g in 1 CARTON 2026-05-15 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
ProBliva Folliculitis .shampoo. 6 g/300g; 3 g/300gthis 85464-0006-01 CAVTECH 300 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
May 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 8Z5ZAL5H3V
    A synthetic polymer made from acrylate compounds. It acts as a thickener and stabilizer in topical formulations, helping create the right texture and prevent separation of ingredients.
  • UNII 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII Q7AO2R1M0B
    Ammonium lauryl sulfate is a mild detergent and foaming agent derived from plant oils. It helps mix water and oil-based ingredients together and creates a light foam in topical formulations like shampoos and cleansers.
  • UNII 3V7U636DWN
    A silicone-based ingredient that acts as a glidant and lubricant. It helps the tablet or capsule slide smoothly during manufacturing and may improve how the medicine flows through equipment.
  • 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 79G1T427CF
    A foaming and cleansing agent derived from coconut oil. It's used in topical products as a thickener and to help create lather or improve how the formula spreads on skin.
  • 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 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII OSA9UP217S
    Dimethiconol is a silicone-based lubricant and anti-foaming agent. It reduces friction between tablet components and prevents foam formation during manufacturing and storage.
  • UNII P160Q81342
    A synthetic cleaning agent derived from lauryl alcohol and succinic acid. It acts as a surfactant and emulsifier to help blend oil and water components, and may aid in drug dissolution and absorption in liquid or semi-solid formulations.
  • 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 M2F465ROXU
    A phosphorus-containing compound used as a chelating agent and water softener in pharmaceutical formulations. It helps prevent mineral buildup and stabilizes the medicine by binding to metal ions that could otherwise degrade the product.
  • 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 13W7MDN21W
    A waxy compound made from glycol and stearic acid. It's used as an emulsifier to help blend oil and water-based ingredients, and as a thickener to give the medicine its desired texture and consistency.
  • UNII B16G315W7A
    A plant-derived thickener made from guar gum that has been chemically modified to carry a positive charge. It's used in medicines as a thickening agent and to help keep ingredients evenly mixed throughout the product.
  • UNII G6Z4KL1252
    A synthetic salt compound used as a formulation aid in medications. It works as a solubilizer and stabilizer to help keep active ingredients dissolved and maintain product stability during storage.
  • UNII ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII 23D6XVI233
    Lauramidopropyl betaine is a mild cleanser and foaming agent derived from coconut oil. In medicines, it helps create a smooth texture, reduce foam, and improve how the product spreads or mixes.
  • UNII N72LMW566G
    A synthetic cleansing agent derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oil and water-based ingredients in liquid medicines, acting as an emulsifier and solubilizer.
  • UNII 178A96NLP2
    Lauryl alcohol is a fatty alcohol derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping blend oil and water-based ingredients and giving the product a smooth, creamy texture.
  • UNII 1DI56QDM62
    A natural fatty substance from soybeans that helps mix oil and water-based ingredients together. It acts as an emulsifier and lubricant in medicines to improve texture and help the product break down properly in your body.
  • UNII VIF565UC2G
    Tea tree oil is an essential oil extracted from the leaves of the Australian tea tree plant. In medicines, it typically serves as a flavoring agent, fragrance, or antimicrobial component in topical formulations.
  • UNII 5DHE01JX1V
    A synthetic surfactant derived from oleic acid and ethylene oxide. It helps dissolve or disperse oils and other hard-to-mix ingredients in liquid medicines, improving uniformity and stability.
  • UNII 8L4OOQ76AM
    A waxy compound made from polyethylene glycol and stearic acid that acts as an emulsifier and thickener. It helps blend oil and water-based ingredients together and gives the medicine its proper texture and consistency.
  • 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 GMR4PEN8PK
    A synthetic polymer used as a thickener and film-former in liquid formulations. It increases viscosity to improve texture and help the medicine spread or adhere evenly on the skin or mucous membranes.
  • UNII 0L414VCS5Y
    A synthetic polymer used as a film-former and conditioning agent. It helps create a protective coating on hair or skin surfaces and improves texture and manageability in topical formulations.
  • UNII OJ245FE5EU
    Sodium benzoate is a salt derived from benzoic acid, a preservative. It's added to medicines to prevent growth of bacteria, fungi, and other microorganisms that could spoil the product.
  • 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 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 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 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII 0YPR65R21J
    Sodium sulfate is a mineral salt used in pharmaceuticals as a filler and diluent. It helps provide bulk and stability to tablets and capsules while remaining inert in the body.
  • UNII 8HM7ZD48HN
    A synthetic surfactant made from tea (triethanolamine) and a long-chain organic compound. It reduces surface tension to help distribute and dissolve active ingredients evenly throughout the medicine.
  • UNII EQR32Y7H0M
    Zinc carbonate is an inorganic mineral compound. It's used in medicines as a buffer and absorbent to help maintain pH balance and control moisture in solid dosage forms.
  • UNII 681VJX72FE
    Zinc glycinate is a mineral compound combining zinc with the amino acid glycine. It serves as a nutrient supplement and may help improve mineral absorption in the formulation.
  • UNII 4YOP58Y695
    Zinc laurate is a salt compound made from zinc and lauric acid, a fatty acid. It acts as a lubricant and glidant in tablets and capsules to reduce friction during manufacturing and improve powder flow.

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

The official label also statesAqua, Sodium Laureth Sulfate, Glycerin, Ammonium Lauryl Sulfate,Sodium Lauryl Sulfate, Lauramidopropyl Betaine, Sodium Chloride,Dimethiconol, Phenoxyethanol, Dimethicone, Sodium Hydroxide, Glycol Distearate, Sodium Benzoate, Melaleuca Alternifolia (Tea Tree) Leaf Oil,Allantoin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium Lauryl Sulfosuccinate, PEG-150 Pentaerythrityl Tetrastearate,Hydrogenated Castor Oil, Amodimethicone, Polyquaternium-10,Hexadimethrine Chloride, Guar Hydroxypropyltrimonium Chloride,Oleth-8, Etidronic Acid, Cocamidopropyl Betaine, Cocamide Methyl MEA, TEA-Dodecylbenzenesulfonate, Laureth-23, Sodium Sulfate,Polyquaternium-7, Zinc Glycinate, Lauryl Alcohol, Zinc Carbonate, ZincLaurate, Ethylhexylglycerin, Hydrogenated Lecithin

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

LabelerCAVTECH HOLDING LLC
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85464
First marketedMay 2026
Product typeHuman Otc Drug
Portfolio11 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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 32 words ▾

Wet hair and scalp thoroughly Massage a small amount into the scalp, leave 2-3 minutes, then rinse For best results use at least twice a week or as directed by a doctor

⏱️ Dosage and Administration 28 words ▾

Helps purify clogged follicles and reduce flaking Soothes redness, itchiness, and scalp irritation Supports a clean, balanced scalp environment For relief of Folliculitis, Seborrheic Dermatitis, Psoriasis and Dandruff

⚠️ Warnings 82 words ▾

For external use only When using this product avoid contact with the eyes If contact occurs, rinse thoroughly with water. Stop and ask a doctor if condition worsens or does not improve after regular use of this product as directed ifcondition cover a large area of the body, consult your doctor before using this product Do not use on broken, irritated, or severly damaged scalp if allergic to any ingredients on children under 2 years of age unless dircted by a doctor

🧪 Active Ingredient 6 words ▾

Selenium Disulfide 1% Salicy Acid 2%

🧪 Inactive Ingredients 67 words ▾

Aqua, Sodium Laureth Sulfate, Glycerin, Ammonium Lauryl Sulfate,Sodium Lauryl Sulfate, Lauramidopropyl Betaine, Sodium Chloride,Dimethiconol, Phenoxyethanol, Dimethicone, Sodium Hydroxide, Glycol Distearate, Sodium Benzoate, Melaleuca Alternifolia (Tea Tree) Leaf Oil,Allantoin, Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Disodium Lauryl Sulfosuccinate, PEG-150 Pentaerythrityl Tetrastearate,Hydrogenated Castor Oil, Amodimethicone, Polyquaternium-10,Hexadimethrine Chloride, Guar Hydroxypropyltrimonium Chloride,Oleth-8, Etidronic Acid, Cocamidopropyl Betaine, Cocamide Methyl MEA, TEA-Dodecylbenzenesulfonate, Laureth-23, Sodium Sulfate,Polyquaternium-7, Zinc Glycinate, Lauryl Alcohol, Zinc Carbonate, ZincLaurate, Ethylhexylglycerin, Hydrogenated Lecithin

🎯 Purpose 6 words ▾

Anti-Dandruff / Seborrheic Dermatitis / Psoriasis

📄 Keep Out of Reach of Children 6 words ▾

Keep out of reach of children

📄 Other Information 19 words ▾

Store at room temperature (15°-30°C/ 59°-86°F) Protect from excessive heat and direct sunlight Keep out of reach of children

📄 Questions or Comments 2 words ▾

[email protected] www.problivabeauty.com

📄 Package Label / Principal Display Panel 1 words ▾

package

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

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 CAVTECH HOLDING LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
CAVTECH HOLDING 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.
← 85464-0005-01 · CAVTECH 85464-0007-01 · CAVTECH →
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.