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VENROCK Piroctone Olamine and Salicylic Acid .5 g/100g; 1.5 g/100g Spray, 1 g — NDC 85772-0002-01 package photo

VENROCK Piroctone Olamine and Salicylic Acid .5 g/100g; 1.5 g/100g Spray, 1 g

by Guangzhou Oupeng Cosmetics Co., Ltd. · 1 g in 1 BOX (85772-0002-1)
NDC 85772-0002-01
🏷️ FDA NDC (as labeled) 85772-0002-1 billing pads the package 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 85772-0002-1
Product NDC 85772-0002
11-digit billing NDC 85772000201
RxCUI 2717186
UNII A4V5C6R9FB, O414PZ4LPZ
Application # M032
SPL Set ID 372feca7-f6f1-cd38-e063-6294a90a3bfe
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-06-20
Route CUTANEOUS, TOPICAL
Dosage form SPRAY
Substance PIROCTONE OLAMINE; SALICYLIC ACID
Why two NDCs? The FDA registers this code as 85772-0002-1 — a 5-4-1 layout, and that's what's printed on the package and shown on DailyMed. For insurance claims, every NDC is standardized to a uniform 11-digit 5-4-2 format by adding a zero to the package segment → 85772-0002-01. 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.

🏭 Manufacturer & labeler

LabelerGuangzhou Oupeng Cosmetics Co., Ltd.
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85772
First marketedJun 2025
Product typeHuman Otc Drug
Portfolio8 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 is this product?

Venrock is a topical spray containing piroctone olamine and salicylic acid, marketed as an over-the-counter monograph drug. Piroctone olamine is typically used in scalp and skin care products for its antimicrobial properties, while salicylic acid is commonly used to help soften and loosen the outer layer of skin. Together, these ingredients are often found in products intended to address scalp conditions and similar skin concerns.

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.

🧪 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.

  • 3 g / 100 g UNII 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • 86.5 g / 100 g 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.
  • 0.3 g / 100 g UNII 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • 0.3 g / 100 g 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.
  • 0.8 g / 100 g UNII 51D0RGY52V
    Camphor leaf oil is a volatile liquid extracted from camphor tree leaves. It functions as a flavoring agent and fragrance in medicines, and may help preserve the product by inhibiting microbial growth.
  • 0.45 g / 100 g UNII H2KVQ74JM4
    A compound derived from coconut oil that acts as a conditioning agent and surfactant. It helps stabilize and thicken liquid formulations while reducing static and improving texture in topical products.
  • 0.25 g / 100 g UNII 6559FC0U1B
    A plant extract from the gentiana macrophylla root used in traditional medicine formulations. It typically serves as a flavoring agent or botanical ingredient to add taste and traditional properties to the medicine.
  • 0.25 g / 100 g UNII GXZ33VNT92
    Gentiana scabra root is a plant extract used in some formulations as a flavoring agent and natural colorant. It may also serve to support the product's stability and shelf life.
  • 1.2 g / 100 g UNII TV85Z17HAZ
    A synthetic emulsifier and humectant derived from glycerin and plant oils. It helps blend oil and water components in formulations and improves moisture retention in topical products.
  • 0.5 g / 100 g 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.
  • 0.5 g / 100 g 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.
  • 1.2 g / 100 g UNII 7YC686GQ8F
    A synthetic oily substance made from castor oil. It works as a solubilizer and emulsifier to help mix oily and water-based ingredients together in the medicine.
  • 2.5 g / 100 g 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.
  • 0.25 g / 100 g UNII U0787KJ43Q
    A plant extract from the Swertia chirayita leaf, used in traditional herbal formulations. It may serve as a flavoring agent or herbal ingredient to support the product's intended botanical composition.

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

The official label also statesAQUA, ALCOHOL, PROPYLENE GLYCOL, SALICYLIC ACID, PEG-40 HYDROGENATED CASTOR OIL, GLYCERETH-25 PCA ISOSTEARATE, CINNAMOMUM CAMPHORA (CAMPHOR) LEAF OIL, PHENOXYETHANOL, MENTHOL, COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, PIROCTONE OLAMINE, BENZOIC ACID, BUTYLENE GLYCOL, SWERTIA CHIRATA EXTRACT, GENTIANA MACROPHYLLA ROOT EXTRACT, GENTIANA SCABRA EXTRACT

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.

💲 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
Venrock .5 g/100g; 1.5 g/100gthis 85772-0002-01 Guangzhou 1 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

🏛️
2025
On the market since
Jun 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
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.

🔬 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 VENROCK (this brand).

Top reported reactions

Vomiting216
Weight Increased212
Pruritus206
Weight Decreased189
Condition Aggravated185
Urticaria184
Headache183

Age at onset

Neonate7
Infant1
Child8
Adolescent6
Adult178
Elderly98

Reporter sex

1,924 reports
Male · 36%
Female · 63%
Unknown · 0%

Serious outcomes

Hospitalization630
Life-threatening176
Disabling124
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 259 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
85772-0002-01 You're viewing this 1 g in 1 BOX (85772-0002-1) 2025-06-20 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 85772-0002-1, 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: 85772-0002-01, written without dashes as 85772000201. 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 85772-0002-01, the first segment (85772) is the labeler code FDA assigned to Guangzhou Oupeng Cosmetics Co., Ltd.; the middle segment (0002) 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 Guangzhou Oupeng Cosmetics Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Oupeng Cosmetics Co., Ltd. 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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 22 words ▾

Uses Helps prevent and control recurrence of the symptoms of dandruff Helps prevent recurrence of the flaking and itching associated with dandruff

⏱️ Dosage and Administration 64 words ▾

Directions Shake well before use Apply to affected areas one to four times daily or as directed by a doctor For best results, use at least twice a week or as directed by a doctor Application: Hold 15-20 cm (4-6 inches) from dry scalp and spray onto affected areas. Use fingertips to massage into scalp for 1-2 minutes until fully absorbed. Do not rinse.

⚠️ Warnings 69 words ▾

Warnings For external use only. Do not use On scalp that is broken or inflamed On children under 12 years of age If you are pregnant When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water ​Avoid contact with mucous membranes. Stop use and ask a doctor if Condition worsens or does not improve after regular use ​Allergic reaction occurs or irritation persists

🧪 Active Ingredient 8 words ▾

Active ingredient(s) Piroctone Olamine 0.5% Salicylic Acid 1.5%

🧪 Inactive Ingredients 42 words ▾

Inactive ingredients AQUA, ALCOHOL, PROPYLENE GLYCOL, SALICYLIC ACID, PEG-40 HYDROGENATED CASTOR OIL, GLYCERETH-25 PCA ISOSTEARATE, CINNAMOMUM CAMPHORA (CAMPHOR) LEAF OIL, PHENOXYETHANOL, MENTHOL, COCAMIDOPROPYL PG-DIMONIUM CHLORIDE PHOSPHATE, PIROCTONE OLAMINE, BENZOIC ACID, BUTYLENE GLYCOL, SWERTIA CHIRATA EXTRACT, GENTIANA MACROPHYLLA ROOT EXTRACT, GENTIANA SCABRA EXTRACT

🎯 Purpose 11 words ▾

Purpose(s) Anti-dandruff (dissolves oil plugs and unclogs pores) Anti-dandruff (inhibits Malassezia)

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85772-0001-01 · Guangzhou 85772-0003-01 · Guangzhou →
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.