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Restoring Pyrithione Zinc .125 g/100mL Liquid, 60 mL — NDC 73528-0410-04 package photo

Restoring Pyrithione Zinc .125 g/100mL Liquid, 60 mL

by Zero Flakes Given, Inc. · 60 mL in 1 TUBE (73528-410-04)
NDC 73528-0410-04
🏷️ FDA NDC (as labeled) 73528-410-04 billing pads the product segment with a zero
This package
Contains60 mL Pack sizes4 compare ↓
Also comes in: 5 ml 73528-0410-03 30 ml 73528-0410-02 100 ml 73528-0410-01
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) 73528-410-04
Product NDC 73528-410
11-digit billing NDC 73528041004
RxCUI 2741467
UNII R953O2RHZ5
Application # M032
SPL Set ID 4f9934e4-ec37-9f68-e063-6394a90ab9a4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-04-30
Route TOPICAL
Dosage form LIQUID
Substance PYRITHIONE ZINC
Why two NDCs? The FDA registers this code as 73528-410-04 — 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 → 73528-0410-04. 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 dermatologicals class.

Drug family (ATC) Other dermatologicals
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

LabelerZero Flakes Given, Inc.
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code73528
First marketedApr 2026
Product typeHuman Otc Drug
Portfolio3 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?

This is a topical liquid product containing pyrithione zinc, an over-the-counter monograph drug marketed under FDA category rules for its ingredient class. Pyrithione zinc is commonly used in topical products to help reduce flaking and itching associated with scalp conditions. The liquid formulation allows for direct application to affected skin or scalp areas. Products containing this ingredient are typically used as part of regular hair or skin care routines.

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.

  • 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 V14F8G75P4
    A fragrant alcohol compound derived from plants or made synthetically. It's used as a flavor and aroma agent to improve the taste and smell of medicines.
  • UNII 79173B4107
    A liquid organic solvent derived from eight-carbon compound. It helps dissolve or carry active ingredients in liquid medicine formulations and may aid in extraction processes during manufacturing.
  • 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 5TJD82A1ET
    A cooling crystalline substance made synthetically that is added to medicines as a fragrance, flavoring agent, and mild local irritant to produce a cooling or warming sensation on the skin or mucous membranes.
  • UNII C9H2L21V7U
    A fat derived from coconut or palm oil containing shorter fatty acid chains. It serves as a solvent and carrier to help dissolve or suspend active ingredients, improving absorption and stability in liquid formulations.
  • 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 I9GRO824LL
    Lemon oil is a natural fragrant extract from lemon peel. It's used in medicines as a flavoring agent to mask unpleasant tastes and improve how the medicine tastes to patients.
  • UNII E107L85C40
    Dipropylene glycol is a clear liquid made from propylene glycol. It acts as a solvent and humectant in medicines, helping dissolve active ingredients and retain moisture in the formulation.
  • UNII C278QS9YBT
    A plant extract from narrow-leaved willowherb used as a natural filler and botanical ingredient in supplements and medicines to add bulk and provide plant-derived material to the formulation.
  • UNII L837108USY
    Geraniol is a natural fragrant compound found in plants like roses and lemons. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII 3W81YG7P9R
    Geranyl acetate is a fragrant compound derived from natural plant sources. It is used in medicines as a flavoring agent to improve taste or as a fragrance component.
  • UNII WQ29KQ9POT
    Gluconolactone is a mild organic acid derived from glucose. It functions as a buffer and pH regulator in medicines, helping maintain stable acidity levels and improve product stability.
  • 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 7U7KU3MWT0
    Hexyl acetate is a synthetic liquid compound used as a solvent and flavoring agent in medicines. It helps dissolve other ingredients and can contribute to the taste or aroma of the formulation.
  • UNII 52JDS841PX
    A spice derived from the star-shaped fruit of the illicium verum plant. It's used in medicines as a flavoring agent to improve taste and sometimes as an ingredient that helps with formulation stability.
  • UNII 9RES347CKG
    A fragrant oil derived from lavandin plants, used as a flavoring and aromatic agent to improve the taste and smell of medicines.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII D2QHA03458
    A fermented ingredient made by culturing beneficial bacteria in radish root extract. It acts as a natural preservative and humectant, helping keep the product fresh and maintain moisture in the formula.
  • UNII 9MC3I34447
    A natural oil extracted from citrus peel, used as a flavoring agent and solvent to improve taste and help dissolve or distribute other ingredients in the medicine.
  • UNII D81QY6I88E
    Linalool is a natural fragrant oil found in plants like lavender and citrus. It's used in medicines as a flavoring agent and to mask unpleasant tastes or smells.
  • UNII 5K47SSQ51G
    A fragrant compound found in plants like lavender and bergamot. It's used as a flavoring and aroma agent to improve the taste and smell of medications.
  • UNII AV092KU4JH
    A natural oil extracted from peppermint plants. It's used as a flavoring agent to mask bitter tastes and add a refreshing mint flavor to medicines, making them easier to take.
  • 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 25X51I8RD4
    Niacinamide is a form of vitamin B3, a water-soluble nutrient. In medicines, it may be added as a nutritional supplement or to support skin health, though its primary role here is as an active ingredient rather than a traditional inactive filler.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 7Q50F46595
    Pea protein is a plant-based powder extracted from peas. It's used as a binder and filler in tablets and capsules to hold ingredients together and add bulk to the formulation.
  • UNII OK17S3S98K
    A waxy, fatty substance derived from plant or animal sources. It acts as a lubricant and glidant to help the medicine flow smoothly during manufacturing and tablet compression.
  • UNII 996299PUKB
    Pinene is a natural oil compound found in pine trees and other plants. It's used in medicines as a flavoring agent and to help mask bitter or unpleasant tastes.
  • UNII J21YE3W98E
    Pisum sativum is a plant-derived ingredient commonly known as garden pea. It's used in medicines as a binder and filler to help hold the tablet together and add bulk to the formulation.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII 1VPU26JZZ4
    Potassium sorbate is a salt derived from sorbic acid, a naturally occurring preservative. It prevents growth of mold, yeast, and some bacteria, extending the medicine's shelf life.
  • UNII 5965N8W85T
    Propanediol is a clear liquid organic compound derived from vegetable sources or synthesized chemically. It acts as a humectant to retain moisture, a solvent to dissolve active ingredients, and a preservative booster in liquid medications and supplements.
  • 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 O2ZTS50U5E
    A plant extract from pomegranate fruit used as a natural coloring agent and flavor component in medications. It may also provide antioxidant properties to help preserve the medicine's stability.
  • UNII 86R5J6D01D
    A plant extract from radish used as a natural flavor and color ingredient in medicines. It may help mask bitter tastes or add mild flavor to oral formulations.
  • UNII EA3289138M
    A plant extract from rosemary that acts as a natural preservative and antioxidant in medicines. It helps prevent oils and fats in the formulation from breaking down and going bad.
  • UNII O414PZ4LPZ
    A beta hydroxy acid derived from willow bark or synthesized chemically. In topical medicines, it acts as a keratolytic agent that helps soften and shed dead skin cells, improving penetration of active ingredients.
  • UNII U27K0H1H2O
    Sage oil is a plant-derived liquid extracted from sage leaves. It's used in medicines as a flavoring agent and preservative to improve taste and help protect the product from spoilage.
  • 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 D3F8YRX7TP
    A salt compound derived from naphthalene that acts as a wetting agent and dispersant. It helps medicines dissolve and spread evenly in liquid formulations.
  • UNII NG5NG5733T
    A synthetic polymer derived from acrylic acid and taurine. It functions as a suspending agent and emulsifier, helping keep ingredients evenly distributed and preventing separation in liquid or semi-solid medicines.
  • UNII R53Q4ZWC99
    Terpineol is a fragrant alcohol derived from pine oil or other plant sources. It's used in medicines as a flavoring agent and to improve the taste or aroma of the product.
  • UNII CHI530446X
    Vanillin is a natural or synthetic aromatic compound that gives vanilla flavor. It's used in medicines as a flavoring agent to mask bitter tastes and improve how the medicine tastes.
  • 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.
  • UNII 3NY3SM6B8U
    A microorganism used as a natural source of B vitamins and proteins. In medications, yeast serves as a nutrient supplement and may help with tablet binding or act as a filler to give the product proper form and stability.

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

The official label also statesInactive Ingredients Water, Aloe Barbadensis Leaf Juice, Propanediol, Glycerin, Gluconolactone, Sodium Polyacryloyldimethyl Taurate, Niacinamide, Salicylic Acid, Butylene Glycol, Sodium Benzoate, Xanthan Gum, Caprylic/Capric Triglyceride, Panthenol, Potassium Hydroxide,Pisum Sativum (Pea) Peptide, Punica Granatum Extract, Yeast Ferment Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Cetearamidoethyl Diethonium Succinoyl Hydrolyzed Pea Protein, Rosmarinus Officinalis (Rosemary) Leaf Extract, Propylene Glycol, Citric Acid, Potassium Sorbate, Raphanus Sativus (Radish) Root Extract, Leuconostoc/Radish Root Ferment Filtrate, 1,2-Hexanediol, Caprylyl Glycol, Sodium Polynaphthanlenesulfonate, Sodium Chloride, Camphor, Citrus Limon (Lemon) Peel Oil, Geranyl Acetate, Lavandula Oil/Extract, Limonene, Linalyl Acetate, Linalool, Mentha Piperita (Peppermint) Oil, Menthol, Terpineol, Vanillin, Lavandin Abrielis Oil, Illicium Verum (Anise) Fruit/Seed Oil, Dipropylene Glycol, Pentadecalactone, Geraniol, Hexyl Acetate, Ethyl Amyl Ketone, Salvia Officinalis (Sage) Oil, 3-Hexenol, Pinene

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.
Try another pack size: 5 ml 30 ml 100 ml
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
Restoring .125 g/100mLthis 73528-0410-04 Zero 60 ml — — 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
Apr 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.

🔬 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 Restoring (this brand).

Top reported reactions

Nausea3
Death2
Dehydration2
Drug Interaction2
Gastrointestinal Disorder2
Headache2
Insomnia2

Age at onset

Adult2
Elderly2

Reporter sex

31 reports
Male · 68%
Female · 32%

Serious outcomes

Death3
Disabling2
Life-threatening1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 7 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
73528-0410-01 100 mL in 1 TUBE (73528-410-01) 2026-04-30 Active
73528-0410-02 30 mL in 1 TUBE (73528-410-02) 2026-04-30 Active
73528-0410-03 5 mL in 1 PACKET (73528-410-03) 2026-04-30 Active
73528-0410-04 You're viewing this 60 mL in 1 TUBE (73528-410-04) 2026-04-30 Active

You're viewing one of 4 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 73528-0410-04?
NDC 73528-0410-04 contains 60 mL — 60 ml in 1 tube.
What is the difference between NDC 73528-0410-04 and NDC 73528-0410-03?
Both are Restoring Pyrithione Zinc .125 g/100mL Liquid — the drug itself is identical. NDC 73528-0410-04 is the 60 mL package, while NDC 73528-0410-03 is the 5 ml package.
What NDC number is used to bill for this package of Restoring Pyrithione Zinc .125 g/100mL Liquid?
Bill NDC 73528-0410-04 — the 11-digit billing format is 73528041004. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 73528-410-04, 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: 73528-0410-04, written without dashes as 73528041004. 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 73528-0410-04, the first segment (73528) is the labeler code FDA assigned to Zero Flakes Given, Inc.; the middle segment (0410) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (04) 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 Zero Flakes Given, Inc.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 3 other package presentations of this same product, including 5 ml (73528-0410-03), 30 ml (73528-0410-02), 100 ml (73528-0410-01). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Zero Flakes Given, Inc. 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 19 words ▾

Uses Uses For relief, and to help prevent reoccurance, of flaking and itching associated with dandruff and seborrheic dermatitis

⏱️ Dosage and Administration 27 words ▾

Directions Directions Apply a thin layer across the scalp (dry or damp). Gently massage in and leave on. Repeat if desired up to four times a day.

⚠️ Warnings 61 words ▾

Warnings For external use only When using this product avoid contact with eyes. If contact occurs rinse eyes thoroughly with water Stop use and ask a doctor if condition worsens or does not improve after regular use of this product as directed Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away

🧪 Active Ingredient 11 words ▾

Active Ingredient Active Ingredient Purpose Pyrithione Zinc 0.125% Anti-Dandruff, Anti-seborrheic dermatitis

🧪 Inactive Ingredients 117 words ▾

Inactive Ingredients Water, Aloe Barbadensis Leaf Juice, Propanediol, Glycerin, Gluconolactone, Sodium Polyacryloyldimethyl Taurate, Niacinamide, Salicylic Acid, Butylene Glycol, Sodium Benzoate, Xanthan Gum, Caprylic/Capric Triglyceride, Panthenol, Potassium Hydroxide,Pisum Sativum (Pea) Peptide, Punica Granatum Extract, Yeast Ferment Extract, Epilobium Angustifolium Flower/Leaf/Stem Extract, Cetearamidoethyl Diethonium Succinoyl Hydrolyzed Pea Protein, Rosmarinus Officinalis (Rosemary) Leaf Extract, Propylene Glycol, Citric Acid, Potassium Sorbate, Raphanus Sativus (Radish) Root Extract, Leuconostoc/Radish Root Ferment Filtrate, 1,2-Hexanediol, Caprylyl Glycol, Sodium Polynaphthanlenesulfonate, Sodium Chloride, Camphor, Citrus Limon (Lemon) Peel Oil, Geranyl Acetate, Lavandula Oil/Extract, Limonene, Linalyl Acetate, Linalool, Mentha Piperita (Peppermint) Oil, Menthol, Terpineol, Vanillin, Lavandin Abrielis Oil, Illicium Verum (Anise) Fruit/Seed Oil, Dipropylene Glycol, Pentadecalactone, Geraniol, Hexyl Acetate, Ethyl Amyl Ketone, Salvia Officinalis (Sage) Oil, 3-Hexenol, Pinene

🎯 Purpose 9 words ▾

Active Ingredient Purpose Pyrithione Zinc 0.125% Anti-Dandruff, Anti-seborrheic dermatitis

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 73528-0110-01 · Zero 73535-0208-01 · Incyte →
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.