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Tuymec Anti-Dandruff Shampoo. 3 g/100mL Shampoo — NDC 87408-0005-01 package photo

Tuymec Anti-Dandruff Shampoo. 3 g/100mL Shampoo

by Guangzhou Jingliang Cosmetics Co., Ltd. · 2 BOTTLE in 1 CARTON (87408-005-01) / 300 mL in 1 BOTTLE
NDC 87408-0005-01
🏷️ FDA NDC (as labeled) 87408-005-01 billing pads the product 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) 87408-005-01
Product NDC 87408-005
11-digit billing NDC 87408000501
UNII O414PZ4LPZ
Application # M032
SPL Set ID 4ae93408-5c8f-c0a5-e063-6394a90a9e0d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-02-16
Route TOPICAL
Dosage form SHAMPOO
Substance SALICYLIC ACID
Why two NDCs? The FDA registers this code as 87408-005-01 — 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 → 87408-0005-01. 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.

🏭 Manufacturer & labeler

LabelerGuangzhou Jingliang Cosmetics Co., Ltd.
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code87408
First marketedFeb 2026
Product typeHuman Otc Drug
Portfolio33 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?

Tuymec Anti-Dandruff Shampoo is a topical shampoo formulated with salicylic acid. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rule-book for its category rather than being individually reviewed by the agency. Salicylic acid is typically used in dandruff and scaling shampoos to help soften and loosen flaky skin on the scalp.

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 459EF9MP3Y
    A synthetic surfactant derived from plant oils, used as an emulsifier and solubilizer to help mix oil and water components together in the medicine formulation.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • 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 CXS4LJR7EL
    Coptis chinensis root is a plant extract used as a natural flavoring and preservative agent in some medicines. It may help preserve product stability and add a bitter taste component to the formulation.
  • UNII 1R81RPY10G
    A waxy substance derived from animal fat that has been chemically processed. It acts as a lubricant and glidant in tablets and capsules, helping the medicine flow smoothly during manufacturing and preventing ingredients from sticking together.
  • 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 A3ULP0F556
    Eculizumab is a manufactured protein that blocks a specific immune system pathway. In this medicine, it serves as the active therapeutic ingredient rather than a typical inactive filler or binder.
  • UNII J1UK54JBGH
    A plant-derived ingredient from fennel seeds used to add flavor and aroma to medicines. It may also have mild preservative properties in some formulations.
  • 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 0324G66D0E
    Glycol stearate is a waxy compound made by combining stearic acid with ethylene glycol. It acts as an emulsifier and thickener, helping keep oil and water mixed together smoothly in liquid or semi-solid medicines.
  • 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 023XA5Z50L
    Hexamidine diisethionate is a synthetic antimicrobial compound used as a preservative in medicines. It prevents bacterial and fungal growth to maintain product safety and stability during storage.
  • UNII O3E12ZLW5T
    A plant extract from houttuynia cordata, an herb used in traditional Asian medicine. It may serve as a natural flavoring agent or botanical additive in 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 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 40KQ7Q535O
    A plant extract from white water lily flowers. It's used in formulations for its soothing and skin-conditioning properties, often included in topical products as a natural ingredient to enhance texture and feel.
  • UNII P9T4K47OM0
    A plant extract from Asian ginseng root. Used as a flavor ingredient and to add aroma to the medicine.
  • 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 X23X6CW68R
    A plant-derived ingredient from bistorta root, used as a binder and thickening agent to help hold tablet ingredients together and improve the product's consistency and texture.
  • UNII A47JP5ZG9M
    A plant-derived ingredient from rhubarb root. Used as a natural colorant and flavoring agent in medicines, and may help the tablet hold its shape during manufacturing.
  • 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 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 4E8QL88U6H
    Taraxacum mongolicum whole is a dried plant material from the dandelion family. It's included as a filler and natural ingredient to add bulk and volume to the formulation.
  • 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 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.

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

The official label also statesWater, Sodium Laureth Sulfate, Cetearyl Alcohol, Dimethicone, Glycol Distearate, Glycol Stearate, Sodium Lauroamphoacetate, Di(Hydrogenated Tallow) Phthalic Acid Amide, C12-15 Alkyl Eth-3, Menthol, Piroctone Olamine, Glycerin, Guar Hydroxypropyltrimonium Chloride, Coptis Chinensis Extract, Rheum Officinale Extract, Polygonum Multiflorum Root Extract, Houttuynia Cordata Extract, Foeniculum Vulgaris Extract, Taraxacum Mongolicum Extract, Nymphea Alba Flower Extract, Panax Ginseng Root Extract, Tea Tree Essential Oil, Citric Acid, Disodium EDTA.

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
Tuymec Anti-Dandruff Shampoo. 3 g/100mLthis 87408-0005-01 Guangzhou 2 bottles — — 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.

🔬 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 Tuymec Anti-Dandruff Shampoo. (this brand).

Top reported reactions

Alopecia1
Application Site Pruritus1
Hair Growth Abnormal1
Inappropriate Schedule Of Drug Administration1
Skin Irritation1
Wrong Patient Received Medication1

Reporter sex

3 reports
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
87408-0005-01 You're viewing this 2 BOTTLE in 1 CARTON (87408-005-01) / 300 mL in 1 BOTTLE 2026-02-16 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 87408-005-01, 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: 87408-0005-01, written without dashes as 87408000501. 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 87408-0005-01, the first segment (87408) is the labeler code FDA assigned to Guangzhou Jingliang Cosmetics Co., Ltd.; 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 Guangzhou Jingliang Cosmetics Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangzhou Jingliang 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 12 words ▾

Uses Controls and relives symptoms of Dandruff, Psoriasis, Folliculitis and Seborrheic Dermatitis.

⏱️ Dosage and Administration 34 words ▾

Directions ■ Apply shampoo and massage into the scalp. ■ Leave in hair for 3-5 minutes to allow maximum absorption. ■ Rinse thoroughly with water. ■ Use 2-4 times per week or as needed.

⚠️ Warnings 5 words ▾

Warnings For external use only.

🧪 Active Ingredient 5 words ▾

Active Ingredient SALICYLIC ACID 3%

🧪 Inactive Ingredients 65 words ▾

Inactive ingredients Water, Sodium Laureth Sulfate, Cetearyl Alcohol, Dimethicone, Glycol Distearate, Glycol Stearate, Sodium Lauroamphoacetate, Di(Hydrogenated Tallow) Phthalic Acid Amide, C12-15 Alkyl Eth-3, Menthol, Piroctone Olamine, Glycerin, Guar Hydroxypropyltrimonium Chloride, Coptis Chinensis Extract, Rheum Officinale Extract, Polygonum Multiflorum Root Extract, Houttuynia Cordata Extract, Foeniculum Vulgaris Extract, Taraxacum Mongolicum Extract, Nymphea Alba Flower Extract, Panax Ginseng Root Extract, Tea Tree Essential Oil, Citric Acid, Disodium EDTA.

🎯 Purpose 7 words ▾

Purpose Scalp treatment, fights itching and flaking.

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 87408-0004-01 · Guangzhou 87408-0006-01 · 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.