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Tagrid ANTI FUNGAL Zinc Pyrithione,Salicylic Acid .02 g/mL; .01 g/mL Shampoo, 300 mL — NDC 85384-0005-01 package photo

Tagrid ANTI FUNGAL Zinc Pyrithione,Salicylic Acid .02 g/mL; .01 g/mL Shampoo, 300 mL

by TAGRID LLC · 300 mL in 1 BOTTLE (85384-0005-1)
NDC 85384-0005-01
🏷️ FDA NDC (as labeled) 85384-0005-1 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) 85384-0005-1
Product NDC 85384-0005
11-digit billing NDC 85384000501
RxCUI 312885
UNII O414PZ4LPZ, R953O2RHZ5
Application # M032
SPL Set ID 3376b104-1f07-fab3-e063-6394a90a0ca4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-05-22
Route TOPICAL
Dosage form SHAMPOO
Substance SALICYLIC ACID; ZINC PYRITHIONE
Why two NDCs? The FDA registers this code as 85384-0005-1 — 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 → 85384-0005-01. 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 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

LabelerTAGRID LLC
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85384
First marketedMay 2025
Product typeHuman Otc Drug
Portfolio24 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?

Tagrid Anti Fungal is an over-the-counter shampoo containing zinc pyrithione and salicylic acid. Zinc pyrithione is typically used in scalp and skin products to reduce bacteria and fungi, while salicylic acid is commonly used to help shed dead skin cells and clear buildup. This combination shampoo is formulated as an OTC monograph product, meaning it follows established FDA guidelines for this category of anti-fungal scalp treatments.

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 04W97Z676Y
    A plant-derived natural substance from Bassia scoparia fruit used as a glidant and anti-caking agent. It helps powder ingredients flow smoothly and prevents clumping in the tablet or capsule.
  • UNII V1IA3S3CUS
    A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
  • UNII 15HNY2J7SS
    Dryobalanops aromatica resin is a natural plant resin extracted from the Borneo camphor tree. It's used in medicines as a flavoring agent and aromatic component to improve taste or scent.
  • UNII A6W0J6UO7Q
    A plant-derived extract from the fruit of the Chinese honey locust tree. It serves as a natural thickener and emulsifier to help blend ingredients and create a smooth, uniform texture in medicines.
  • UNII J1BO4MHT2L
    A plant material from Canadian mint that provides flavor and aroma to the medicine. It's used to improve taste and make the product more pleasant to take.
  • UNII 32E5V7G32B
    A plant extract from Oriental arborvitae leaves, used in formulations as a natural flavoring agent, fragrance component, or preservative to enhance taste, aroma, or shelf stability.
  • UNII AUZ3VD75MC
    A plant extract from Japanese knotweed root used as a natural colorant and antioxidant in medications. It helps preserve the product and may contribute to the pill's appearance or stability.
  • UNII C61Y66MY4H
    A plant-derived substance from Sauromatum giganteum used as a binder or thickening agent to help hold the medicine together and improve its texture and stability in the formulation.
  • UNII 7S9328671Z
    A plant extract from stemona tuberosa root used as a natural preservative and antimicrobial agent in some formulations to help prevent spoilage and extend shelf life.
  • UNII IN6Q3S3414
    A plant material from ginger root used as a flavoring and aromatic ingredient to improve taste and add natural ginger flavor to medicines.

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

The official label also statesInactive ingredients: Salicylic Acid Zinc Pyrithione Stemona Tuberosa Root Bassia Scoparia Fruit Zingiber Officinale Whole Platycladus Orientalis Leaf Sauromatum Giganteum Whole Reynoutria Multiflora Root Mentha Canadensis Whole Dryobalanops Aromatica Resin Gleditsia Sinensis Fruit Cnidium Monnieri Fruit

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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Tagrid ANTI FUNGAL .02 g/mL; .01 g/mLthis 85384-0005-01 TAGRID 300 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

🏛️
2025
On the market since
May 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
85384-0005-01 You're viewing this 300 mL in 1 BOTTLE (85384-0005-1) 2025-05-22 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 85384-0005-1, 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: 85384-0005-01, written without dashes as 85384000501. 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 85384-0005-01, the first segment (85384) is the labeler code FDA assigned to TAGRID LLC; the middle segment (0005) 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 TAGRID LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TAGRID 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.

📄 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 20 words ▾

Uses: Controls dandruff, flaking, and itching Helps relieve symptoms of seborrheic dermatitis Clears scalp buildup and supports healthy scalp environment

⏱️ Dosage and Administration 29 words ▾

Directions: Shake well before use Apply to wet scalp Gently massage and leave on for 3-5 minutes Rinse thoroughly Use 2-3 times weekly, or as directed by your dermatologist

⚠️ Warnings 78 words ▾

For external use only On broken or irritated skin. Ask a doctor before use if you have: • Sensitive skin When using this product • Avoid contact with eyes. If contact occurs, rinse thoroughly. Stop use and ask a doctor if • Condition worsens or does not improve If pregnant or breast-feeding • Ask a health professional before use Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 8 words ▾

Active ingredient: Zinc Pyrithione 1% Salicylic Acid 2%

🧪 Inactive Ingredients 36 words ▾

Inactive ingredients: Salicylic Acid Zinc Pyrithione Stemona Tuberosa Root Bassia Scoparia Fruit Zingiber Officinale Whole Platycladus Orientalis Leaf Sauromatum Giganteum Whole Reynoutria Multiflora Root Mentha Canadensis Whole Dryobalanops Aromatica Resin Gleditsia Sinensis Fruit Cnidium Monnieri Fruit

🎯 Purpose 19 words ▾

Purpose 1: Anti-Dandruff ( Active ingredient：Zinc Pyrithione 1% ) Purpose 2: Anti-seborrheic dermatitis ( Active ingredient：Salicylic Acid 2% )

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 85384-0004-01 · TAGRID 85384-0006-01 · TAGRID →
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.