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EASYES ANTI-DANDRUFF AND ANTI HAIR-THINNING SHAM-POO 1 mg/100mL Shampoo, 200 mL — NDC 84753-0036-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

EASYES ANTI-DANDRUFF AND ANTI HAIR-THINNING SHAM-POO 1 mg/100mL Shampoo, 200 mL — NDC 84753-036-01 (Billing 84753-0036-01)

by Guangdong Bisutang Biotechnology Co., LTD · 200 mL in 1 BOTTLE

This is a package of 200 mL of EASYES ANTI-DANDRUFF AND ANTI HAIR-THINNING SHAM-POO 1 mg/100mL Shampoo from Guangdong Bisutang Biotechnology Co., LTD, marketed since Aug 2025 and currently FDA-listed. It is this product's only package size.

NDC 84753-0036-01
🏷️ FDA NDC (as labeled) 84753-036-01 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

NDC database record

One package, one record: these facts belong to NDC 84753-036-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
84753 labeler · 036 product · 01 package
Package marketed since
Aug 25, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8475303601 2
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 84753-036-01
Product NDC 84753-036
11-digit billing NDC 84753003601
UNII Z69D9E381Q
Application # 505G(a)(3)
SPL Set ID 3d27b19e-2c64-9822-e063-6394a90a4971
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-08-25
Route TOPICAL
Dosage form SHAMPOO
Substance SELENIUM SULFIDE
Why two NDCs? The FDA registers this code as 84753-036-01 — 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 → 84753-0036-01. 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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It's used on the scalp to relieve flaking and itching from dandruff and seborrheic dermatitis. It also helps keep those problems from coming back. Some products also list relief of...
  • Most labels say to use it at least twice a week for best results, or as your doctor directs. Some say you can use it every time you shampoo for maximum control. Check your own prod...
  • Some people get skin irritation, or oily or dry hair and scalp. Hair discoloration and a bit more hair shedding have been reported occasionally. Rinsing thoroughly after use helps...
  • Keep it out of your eyes and away from the genital area, since it can cause irritation and burning. Don't use it on broken or inflamed skin. If you get it in your eyes, rinse well...
📖 Read our full Selenium Sulfide guide →

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
84753-0036-01 You're viewing this Main listing 200 mL in 1 BOTTLE 2025-08-25 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Easyes Anti-Dandruff And Anti Hair-Thinning Sham-Poo 1 mg/100mLthis 84753-0036-01 Guangdong 200 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
Aug 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.

What it looks like

Color yellow
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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.

🧪 Avoiding an ingredient? See Selenium Sulfide inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

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

  • UNII 3UVP41R77R
    Avena sativa kernel oil is a natural oil extracted from oat seeds. It's used in medicines as an emollient and skin-conditioning agent to help soften and moisturize the product's texture.
  • UNII W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII 7M867G6T1U
    Centella asiatica is a plant extract used in medicines as a skin-conditioning or soothing ingredient. It helps maintain product stability and may support skin comfort in topical formulations.
  • UNII 4370DF050B
    Ceramide NP is a waxy, lipid-based substance that mimics natural skin oils. It's used in topical formulations as an emollient and skin-conditioning agent to help soften, smooth, and protect the skin barrier.
  • 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 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 1756681479
    A chemical compound used in pharmaceutical formulations as an antimicrobial preservative. It helps prevent bacterial and fungal growth, extending the product's shelf life and maintaining stability during storage.
  • UNII 1NKX3648J9
    A synthetic antimicrobial compound used as a preservative in medicines and topical products to prevent bacterial and fungal growth, helping keep the medication safe and effective during storage.
  • UNII M2HW98ZA4V
    Dimethiconol is a silicone-based lubricant and anti-foaming agent. It reduces friction between particles and prevents excess air bubbles in liquid or semi-solid medicines, helping them mix smoothly and stay stable.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII OU4GI2R2WB
    A blend of fragrance compounds that adds a fresh citrus and floral scent to the medicine. Fragrances mask unpleasant tastes or odors to make the product more pleasant to use.
  • 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 13W7MDN21W
    A waxy compound made from glycol and stearic acid. It's used as an emulsifier to help blend oil and water-based ingredients, and as a thickener to give the medicine its desired texture and consistency.
  • 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 ZF94AP8MEY
    Hydrogenated castor oil is a processed plant oil made by adding hydrogen to castor oil. It's used as a binder to help hold tablet ingredients together and as a lubricant to prevent sticking during manufacturing.
  • UNII F32E4CB0UJ
    Laureth-3 is a synthetic surfactant derived from lauryl alcohol. It helps dissolve or blend oils and water-based ingredients in medicines, and may improve how the product spreads on skin or is absorbed.
  • UNII 1160N9NU9U
    Lauric acid is a natural saturated fatty acid derived from coconut or palm oil. It serves as an emulsifier and lubricant in medicines, helping ingredients mix smoothly and preventing sticking during manufacturing.
  • UNII 2C1F12C6AP
    A beneficial live bacterium used as a probiotic ingredient. It's included to support the product's probiotic function by promoting beneficial microorganisms in the digestive system.
  • UNII 7VK9GL8RUP
    A plant-based oil extracted from macadamia nuts. It functions as an emollient and skin-conditioning agent in topical formulations, helping to soften and smooth the product texture.
  • 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 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 D5J3623SV2
    Portulaca oleracea is a plant extract used in medicines as a natural ingredient. It may function as an antioxidant or skin-conditioning agent in topical formulations.
  • UNII G57KL1I9I7
    A plant-derived oil from Prinsepia utilis seeds used as an emollient and lubricant in formulations. It helps soften and smooth the product texture while improving how ingredients blend together.
  • UNII QW70YFP724
    A plant extract used in traditional medicines, derived from the whole Rhinacanthus nasutus plant. It functions as a natural ingredient to support formulation stability and texture.
  • UNII 8LGU7VM393
    Rosemary leaf oil is a natural aromatic oil extracted from rosemary plants. It's used in medicines as a flavoring agent and preservative to 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 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 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII JVL98CG53G
    Sodium methyl cocoyl taurate is a mild, plant-derived cleaning agent made from coconut oil and an amino acid. It's used in liquid formulations as a surfactant to help mix oil and water-based ingredients together and improve how the medicine spreads or is absorbed.
  • UNII WIQ1H85SYP
    A salt form of salicylic acid, sodium salicylate is a chemical compound used in medicines as a buffer or pH regulator. It helps maintain the medicine's stability and proper acidity level during storage and use.
  • UNII X8KX602M5L
    Sophora flavescens is a plant extract used in medicines as a natural thickening agent and skin-conditioning ingredient. It helps adjust the medicine's texture and may support formulation stability.
  • UNII 70FD1KFU70
    Sulfur is a naturally occurring chemical element. It works as an anti-caking agent and preservative in medicines, helping the product stay dry and preventing spoilage.
  • 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.
  • UNII SAS9Z1SVUK
    A natural oil extracted from ginger root that adds flavor and aroma to the medicine. It may also serve as a preservative or help mask unpleasant tastes in the formulation.

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

The official label also statesWATER SODIUM LAURETH SULFATE COCAMIDOPROPYL BETAINE DIMETHICONOL SODIUM CHLORIDE DIAMINOPYRIMIDINE OXIDE SODIUM LAURYL SULFATE SODIUM SALICYLATE GLYCERIN PHENOXYETHANOL GLYCOL DISTEARATE SODIUM BENZOATE FRAGRANCE FRESH CITRUS FLORAL ORC1501495 SODIUM METHYL COCOYL TAURATE HYDROGENATED CASTOR OIL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE ZINC PCA CITRIC ACID LAURETH-3 DICHLOROBENZYL ALCOHOL SULFUR GLYCOL STEARATE LAURIC ACID ETHYLHEXYLGLYCERIN PLATYCLADUS ORIENTALIS LEAF AVENA SATIVA (OAT) KERNEL OIL CENTELLA ASIATICA LIMOSILACTOBACILLUS FERMENTUM CAMELLIA SINENSIS LEAF PORTULACA OLERACEA WHOLE SOPHORA FLAVESCENS WHOLE MACADAMIA INTEGRIFOLIA SEED OIL ZINGIBER OFFICINALE (GINGER) ROOT OIL ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL PRINSEPIA UTILIS SEED CERAMIDE NP RHINACANTHUS NASUTUS WHOLE

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

LabelerGuangdong Bisutang Biotechnology Co., LTD
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code84753
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio9 products on file

More NDCs from Guangdong Bisutang Biotechnology Co., LTD labeler code 84753

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

Fights and helps prevent recurrence ofscalp flaking and itching associated with dandruff.

⏱️ Dosage and Administration 30 words ▾

For best results, use at least twice a week or as directed bya doctor. wet hair and apply small amount of shampoo and massageonto scalp. rinse and repeat if desired.

⚠️ Warnings 54 words ▾

For external use onlyWhen using this product avoid contact with the eyes. lf contact occurs, rinseeyes thoroughly with water, Stop use and ask a doctor if condition worsens ordoes not improve after regular use of this product as directed. Keep outof reach of children.lf swallowed, get medical help or contact a PoisonControl Centerright away.

🧪 Active Ingredient 6 words ▾

Selenium Sulfide 1% Piroctone Olamine 0.2%

🧪 Inactive Ingredients 93 words ▾

WATER SODIUM LAURETH SULFATE COCAMIDOPROPYL BETAINE DIMETHICONOL SODIUM CHLORIDE DIAMINOPYRIMIDINE OXIDE SODIUM LAURYL SULFATE SODIUM SALICYLATE GLYCERIN PHENOXYETHANOL GLYCOL DISTEARATE SODIUM BENZOATE FRAGRANCE FRESH CITRUS FLORAL ORC1501495 SODIUM METHYL COCOYL TAURATE HYDROGENATED CASTOR OIL GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE ZINC PCA CITRIC ACID LAURETH-3 DICHLOROBENZYL ALCOHOL SULFUR GLYCOL STEARATE LAURIC ACID ETHYLHEXYLGLYCERIN PLATYCLADUS ORIENTALIS LEAF AVENA SATIVA (OAT) KERNEL OIL CENTELLA ASIATICA LIMOSILACTOBACILLUS FERMENTUM CAMELLIA SINENSIS LEAF PORTULACA OLERACEA WHOLE SOPHORA FLAVESCENS WHOLE MACADAMIA INTEGRIFOLIA SEED OIL ZINGIBER OFFICINALE (GINGER) ROOT OIL ROSMARINUS OFFICINALIS (ROSEMARY) LEAF OIL PRINSEPIA UTILIS SEED CERAMIDE NP RHINACANTHUS NASUTUS WHOLE

🎯 Purpose 9 words ▾

Helps prevent recurrence ofscalp flaking and itchingassociated with dandruff.

📄 Keep Out of Reach of Children 16 words ▾

Keep outof reach of children.lf swallowed, get medical help or contact a PoisonControl Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

Product images

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 Guangdong Bisutang Biotechnology Co., LTD. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Guangdong Bisutang Biotechnology 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.
← 84753-0034-01 · Guangdong 84753-0037-01 · Guangdong →
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.