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ProBliva Antibacterial and Acne Body Wash .65 g/500g; 2.5 g/500g Shampoo, 500 g — NDC 85464-0004-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

ProBliva Antibacterial and Acne Body Wash .65 g/500g; 2.5 g/500g Shampoo, 500 g — NDC 85464-004-01 (Billing 85464-0004-01)

by CAVTECH HOLDING LLC · 500 g in 1 CARTON

This is a package of 500 g of ProBliva Antibacterial and Acne Body Wash .65 g/500g; 2.5 g/500g Shampoo from CAVTECH HOLDING LLC, marketed since Feb 2026 and currently FDA-listed. It is this product's only package size.

NDC 85464-0004-01
🏷️ FDA NDC (as labeled) 85464-004-01 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) 85464-004-01
Product NDC 85464-004
11-digit billing NDC 85464000401
RxCUI 2735812
UNII F5UM2KM3W7, O414PZ4LPZ
UPC 0850081497004
Application # M006
SPL Set ID 496f7a1e-05b6-d434-e063-6394a90afe54
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-18
Route TOPICAL
Dosage form SHAMPOO
Substance BENZALKONIUM CHLORIDE; SALICYLIC ACID
Quick answers
  • RxCUI (RxNorm): 2735812
Why two NDCs? The FDA registers this code as 85464-004-01 — 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 → 85464-0004-01. 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 Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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 is an over-the-counter shampoo containing benzalkonium chloride and salicylic acid. Benzalkonium chloride is an antimicrobial agent typically used to reduce bacteria on the skin, while salicylic acid is commonly used to help exfoliate skin and unclog pores. Together, these ingredients are often combined in body cleansers and shampoos intended for acne-prone or oily skin areas.

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
85464-0004-01 You're viewing this Main listing 500 g in 1 CARTON 2026-02-18 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
ProBliva Antibacterial and Acne Body Wash .65 g/500g; 2.5 g/500gthis 85464-0004-01 CAVTECH 500 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
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.

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

  • 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 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 94ZLA3W45F
    Arginine is an amino acid used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level and stability of liquid formulations.
  • 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 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 4V023DD7KL
    A plant-derived ingredient from the Asian persimmon fruit. It's used as a natural sweetener, flavor enhancer, and binder to improve taste and help hold the medicine's form together.
  • UNII MBK0CP8F5A
    Disodium cocoyl glutamate is a mild cleanser derived from coconut oil and amino acids. It acts as a surfactant and emulsifier in medicines, helping to mix oil and water-based ingredients together and improve how the product spreads or absorbs.
  • 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 T7S323PKJS
    Hamamelis virginiana is an extract from the witch hazel plant. In medications, it's used as an astringent and skin-soothing agent to help reduce irritation and provide a mild drying effect in topical formulations.
  • UNII 3T47HH21LT
    This is a human enzyme that adds fatty acid groups to ghrelin, a natural hormone in the body. In medications, it may be used to help the drug work more effectively by modifying how ghrelin functions.
  • UNII AAZ2QV38TA
    Hydrolyzed sodium hyaluronate is a salt form of hyaluronic acid, a naturally occurring substance found in connective tissue. In medicines, it serves as a humectant and thickener to improve texture, retain moisture, and enhance product stability.
  • UNII 5307V7XW8I
    A beneficial bacterium added to certain medicines and supplements. It acts as a probiotic ingredient, helping maintain or restore healthy gut bacteria balance in formulations designed for digestive wellness.
  • UNII 76LN7P7UCU
    Lauryl glucoside is a mild plant-based cleansing agent made from coconut oil and glucose. It's used in medicines as a surfactant to help dissolve and distribute ingredients evenly throughout 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 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 1AEY1M553N
    A natural oil extracted from spearmint or field mint leaves, used as a flavoring agent to give medicines a minty taste and aroma. It may also provide a cooling sensation in topical products.
  • 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 A4V5C6R9FB
    Piroctone olamine is a antimicrobial compound used in medicines as a preservative or antifungal agent. It helps prevent bacterial and fungal growth in topical formulations like shampoos and skin products.
  • 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 XLU9KH03XM
    A mild, plant-derived cleansing agent made from coconut oil and the amino acid glycine. It acts as a surfactant and emulsifier to help blend oil and water-based ingredients and improve texture in topical products.
  • UNII SLK428451L
    Sodium lauroamphoacetate is a mild cleaning agent derived from coconut oil. It acts as a surfactant and emulsifier in medicines, helping blend water and oil-based ingredients together and improving how the product spreads or dissolves.
  • UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • UNII B8WCK70T7I
    Trehalose is a natural sugar made from two glucose molecules linked together. It's used in medicines as a filler to add bulk, a sweetener for taste, and a stabilizer to help keep active ingredients effective during storage.
  • 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 C32PQ86DH4
    Zinc PCA is a zinc salt of pyroglutamic acid, a naturally occurring amino acid derivative. It's used in medications as a skin-conditioning agent and to help maintain product stability and texture in topical formulations.

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

The official label also statesWater, Sodium Lauroyl Sarcosinate, Cocamidopropyl Betaine, Lauryl Glucoside, Sodium Cocoyl Glycinate, Sodium Lauroamphoacetate,Cocamide Methyl MEA, Disodium Cocoyl Glutamate, Glycerin, Piroctone Olamine, Sodiumn Chloride, Trehalose, Phenoxyethanol, Panthenol,Hamamells Virginiana (Witch Hazel) Water, Aloe Barbadensis Leaf Julce,Diospyros Kaki Fruit Extract, Sodium Benzoate, Menthol, Arginine,Melaleuca Alternifolia (Tea Tree) Leaf Oil, Mentha Arvensis Extract,Lactobacillus/Rice Ferment, Hydrolyzed Oat Protein, Allantoin, Zinc PCA,Citric Acid, Disodium EDTA, Hydrolyzed Sodium Hyaluronate

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 applicationM006 (OTC MONOGRAPH DRUG)
Labeler code85464
First marketedFeb 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 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 50 words ▾

For use on body only (not for face) Apply to wet skin, work into agentle lather, and massage onto affected areas Leave on for 30seconds to 1 minute, then rinse thoroughly Use once or twice daily,or as directed by a doctor If dryness or peeling occurs, reduce frequency of use

⏱️ Dosage and Administration 30 words ▾

Helps clear up acne blemishes and prevent new breakouts Helps reduce bacteria on the skin that can cause acne and body odor Gently cleanses and purifies oily or acne-prone skin

⚠️ Warnings 109 words ▾

Fore external use only Avoid contact with eyes, lips, and mucous membranes. If contact occurs, rinse thoroughly with water Skin irritation and dryness are more likely to occur If you use another topical acne medication at the same time If irritation occurs, useonly one fopical acne medication at a time This product may causemild tingling or temporary dryness in sensitive skin Stop and ask a doctor if -Severe irrifation or redness develops Condition worsens or does not improve after regular use On broken skin or open wounds lf you are allergic tosalicylic acid or benzalkonium chloride Over large areas of the bodyfor extended periods unless directed by a doctor

🧪 Active Ingredient 6 words ▾

Benzalkonium Chloride 0.13% Salicylic Acid 0.5%

🧪 Inactive Ingredients 62 words ▾

Water, Sodium Lauroyl Sarcosinate, Cocamidopropyl Betaine, Lauryl Glucoside, Sodium Cocoyl Glycinate, Sodium Lauroamphoacetate,Cocamide Methyl MEA, Disodium Cocoyl Glutamate, Glycerin, Piroctone Olamine, Sodiumn Chloride, Trehalose, Phenoxyethanol, Panthenol,Hamamells Virginiana (Witch Hazel) Water, Aloe Barbadensis Leaf Julce,Diospyros Kaki Fruit Extract, Sodium Benzoate, Menthol, Arginine,Melaleuca Alternifolia (Tea Tree) Leaf Oil, Mentha Arvensis Extract,Lactobacillus/Rice Ferment, Hydrolyzed Oat Protein, Allantoin, Zinc PCA,Citric Acid, Disodium EDTA, Hydrolyzed Sodium Hyaluronate

🎯 Purpose 3 words ▾

Antibacterial Acne Treatment

📄 Do Not Use 28 words ▾

On broken skin or open wounds lf you are allergic tosalicylic acid or benzalkonium chloride Over large areas of the bodyfor extended periods unless directed by a doctor

📄 Ask a Doctor Before Use If 20 words ▾

Stop and ask a doctor if -Severe irrifation or redness develops Condition worsens or does not improve after regular use

📄 When Using This Product 57 words ▾

Avoid contact with eyes, lips, and mucous membranes. If contact occurs, rinse thoroughly with water Skin irritation and dryness are more likely to occur If you use another topical acne medication at the same time If irritation occurs, useonly one fopical acne medication at a time This product may causemild tingling or temporary dryness in sensitive skin

📄 Keep Out of Reach of Children 7 words ▾

Keep out of reach of children section.

📄 Other Information 18 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] 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.
← 85464-0003-01 · CAVTECH 85464-0005-01 · 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.