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EASYES ANTI DANDRUFF AND ANTI HAIR THINNING SHAMP00 1 g/100mL Shampoo, 200 mL — NDC 85004-0002-01 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 SHAMP00 1 g/100mL Shampoo, 200 mL — NDC 85004-002-01 (Billing 85004-0002-01)

by Qingyuan Moksha Biotechnology Co., Ltd. · 200 mL in 1 BOTTLE

This is a package of 200 mL of EASYES ANTI DANDRUFF AND ANTI HAIR THINNING SHAMP00 1 g/100mL Shampoo from Qingyuan Moksha Biotechnology Co., Ltd., marketed since Mar 2026 and currently FDA-listed. It is this product's only package size.

NDC 85004-0002-01
🏷️ FDA NDC (as labeled) 85004-002-01 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 85004-002-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
85004 labeler · 002 product · 01 package
Package marketed since
Mar 30, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8500400201 5
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 85004-002-01
Product NDC 85004-002
11-digit billing NDC 85004000201
RxCUI 204642
UNII Z69D9E381Q
Application # M032
SPL Set ID 4e386cc8-004a-9742-e063-6394a90a763c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-03-30
Route CUTANEOUS
Dosage form SHAMPOO
Substance SELENIUM SULFIDE
Quick answers
  • RxCUI (RxNorm): 204642
Why two NDCs? The FDA registers this code as 85004-002-01 — 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 → 85004-0002-01. 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.

RxNorm drug class

This medicine belongs to the Other antifungals for topical use class.

Drug family (ATC) Other antifungals for topical use
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.

Clinical

📖 What it is MedlinePlus · NLM

Selenium sulfide, an anti-infective agent, relieves itching and flaking of the scalp and removes the dry, scaly particles that are commonly referred to as dandruff or seborrhea. It is also used to treat tinea versicolor, a fungal infection of the skin. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.

Read the full MedlinePlus article ↗
📗 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
85004-0002-01 You're viewing this Main listing 200 mL in 1 BOTTLE 2026-03-30 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Rugby Anti-Dandruff 10 mg/mL 00536-1995-53 Rugby 207 ml $0.014 — Availability likely —
Leader Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff 10 mg/mL 70000-0531-01 Cardinal 207 ml $0.014 — Availability likely —
Walgreens Dandruff and Conditioner Cleansing and Conditioning Anti-dandruff 10 mg/mL 00363-4136-01 Walgreen 325 ml — — FDA listed —
Walgreens Dandruff Maximum Strength Anti-dandruff 10 mg/mL 00363-4139-01 Walgreen 325 ml — — FDA listed —
Walgreens Dandruff With Menthol/Selenium Sulfide Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 10 mg/mL 00363-4902-01 Walgreen 325 ml — — FDA listed —
Walgreens Clinical Strength Medicated Dandruff Anti-dandruff, Anti-seborrheic dermatitis 10 mg/mL 00363-9422-01 Walgreen 400 ml — — FDA listed —
Dandruff 10 mg/mL 37808-0816-15 H 420 ml — — FDA listed —
Selsun Blue 2-in-1 1 g/100mL 41167-1651-04 Chattem, 325 ml — — FDA listed —
Selsun Blue Itchy Dry Scalp .01 g/mL 41167-6020-03 Chattem, 325 ml — — FDA listed —
Selsun Blue Moisturizing 1 g/100mL 41167-6032-00 Chattem, 207 ml — — FDA listed —
Selsun Blue Medicated 1 g/100mL 41167-6061-01 Chattem, 325 ml — — FDA listed —
Meijer Medicated Selenium Sulfide Anti-Dandruff 10 mg/mL 41250-0545-01 Meijer 325 ml — — FDA listed —
Dandruff 10 mg/mL 41250-0816-15 Meijer, 420 ml — — FDA listed —
Equate Medicated Dandruff Anti-Dandruff 10 mg/mL 49035-0534-01 Wal-Mart 325 ml — — FDA listed —
GoodSense Medicated Dandruff Anti-Seborrheic Dermatitis, Anti-Dandruff 10 mg/mL 50804-0883-01 GOODSENSE 325 ml — — FDA listed —
CVS Health MAXIMUM STRENGTH Dandruff Anti-Seborrheic Dermatitis, anti-dandruff 10 mg/mL 51316-0387-01 CVS 325 ml — — FDA listed —
CVS Health MAXIMUM STRENGTH Dandruff Medicated Anti-Seborrheic Dermatitis, anti-dandruff 10 mg/mL 51316-0719-01 CVS 325 ml — — FDA listed —
FAMILY Wellness MAXIMUM STRENGTH DANDRUFF Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 10 mg/mL 55319-0949-01 FAMILY 325 ml — — FDA listed —
CVS Gold 1000 mg/100mL 63148-0209-13 Apollo 400 ml — — FDA listed —
Head and Shoulders Clinical Strength Dandruff Defense Dry Scalp Rescue 1 g/100mL 69423-0523-40 The 400 ml — — FDA listed —
Head and Shoulders Clinical Strength Dandruff Defense Advanced Oil Control 1 g/100mL 69423-0525-40 The 400 ml — — Discontinued —
Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief 1 g/100mL 69423-0526-01 The 2 bottles — — FDA listed —
Head and Shoulders 2in1 Clinical Strength Dandruff Defense Intensive Itch Relief 1 g/100mL 69423-0527-40 The 400 ml — — FDA listed —
Head and Shoulders Clinical Strength Dandruff Defense Sensitive Scalp 1 g/100mL 69423-0642-40 The 400 ml — — Discontinued —
Prosoria Medicated 1.77 g/177mL 71573-0121-12 Nuvothera, 177 ml — — FDA listed —
amazon basics maximum strength dandruff Anti-dandruff 10 mg/mL 72288-0551-01 AMAZON.COM 325 ml — — FDA listed —
Careone Medicated Dandruff 10 mg/mL 72476-0025-03 Retail 325 ml — — FDA listed —
Topco Associates 10 mg/mL 76162-0171-11 Topco 325 ml — — FDA listed —
meijer MEDICATED selenium sulfide Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 10 mg/mL 79481-0071-01 Meijer 325 ml — — FDA listed —
up and up Moisturizing Anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 10 mg/mL 82442-0308-01 TARGET 355 ml — — FDA listed —
up and up Medicated Anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis 10 mg/mL 82442-0384-01 TARGET 355 ml — — FDA listed —
Dermoia Seborrheic Dermatitis Selenium Sulfide 10 mg/mL 83524-0938-00 TREASUREWISE 355 ml — — FDA listed —
Head and Shoulders Clinical Strength Advanced Oil Control 1 g/100mL 84126-0075-01 The 2 bottles — — FDA listed —
Head and Shoulders 2in1 Clinical Strength Dry Scalp Rescue 1 g/100mL 84126-0083-40 The 400 ml — — FDA listed —
Head and Shoulders Clinical Strength Dry Scalp Rescue 1 g/100mL 84126-0108-01 The 2 bottles — — FDA listed —
Head and Shoulders Clinical Strength Cooling Itch Relief 1 g/100mL 84126-0183-01 The 2 bottles — — FDA listed —
Head and Shoulders 2in1 Clinical Strength Cooling Itch Relief 1 g/100mL 84126-0184-40 The 400 ml — — FDA listed —
Seleniumdisulfideanti-Dandruffshampoo 1 g/100g 84778-0080-01 Guangzhou 300 g — — Discontinued —
Easyes Anti Dandruff And Anti Hair Thinning Shamp00 1 g/100mLthis 85004-0002-01 Qingyuan 200 ml — — FDA listed —
UCHOIZE S2 Balance Anti-Dandruff 1 g/100mL 85724-0001-01 Dreamwise 280 ml — — FDA listed —
Silvagle Selenium Sulfide Anti DandruffShampoo 1 mg/100mg 87806-0001-01 GUANGZHOU 300 mg — — 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
Mar 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.

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 K72A0BR9CQ
    Beta-methylcholine chloride is a synthetic organic compound that acts as a solvent and preservative in medications. It helps dissolve other ingredients and protect the product from spoilage during storage.
  • 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 344S277G0Z
    Allantoin is a naturally derived compound that helps soften and soothe skin. In medicines, it works as a skin-conditioning agent and may help support wound healing and reduce irritation in topical formulations.
  • UNII Q7AO2R1M0B
    Ammonium lauryl sulfate is a mild detergent and foaming agent derived from plant oils. It helps mix water and oil-based ingredients together and creates a light foam in topical formulations like shampoos and cleansers.
  • UNII VA5T401RWV
    A silicone-based ingredient that reduces friction and improves the texture and flow of powdered or solid medicines. It acts as a glidant and lubricant to help ingredients mix smoothly and tablets compress evenly during manufacturing.
  • UNII EMY54R518C
    A natural extract from bamboo leaves used as a filler and thickening agent in medications. It helps give the product proper texture and consistency while serving as a plant-based inactive ingredient.
  • UNII 26X6QU3JUB
    A beneficial bacterial strain added to support the product's probiotic content. It serves as the active probiotic ingredient, helping maintain the viable cell count needed for the formula's intended effect.
  • UNII BB4PU4V09H
    A plant-derived gum that acts as a thickener and stabilizer in medications. It helps maintain consistent texture and prevents ingredient separation in liquid or semi-solid formulations.
  • UNII 24WE03BX2T
    Levomenol is a naturally derived alcohol compound used as a skin-conditioning and anti-inflammatory agent in topical formulations. It helps soothe and protect the skin while improving product texture and absorption.
  • 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 UPY805K99W
    A synthetic compound derived from caprylic acid that works as a preservative and antimicrobial agent to help prevent bacterial and fungal growth in the medicine.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII ZX5QRE4U60
    A fragrant plant oil derived from cedar bark, used as a natural flavoring and aroma agent in medicines. It helps mask unpleasant tastes and adds pleasant scent to the product.
  • UNII 6810070TYD
    Centella asiatica leaf is a plant extract used in medicines as a skin-conditioning agent and natural ingredient. It may help soften or soothe the product's texture and is included for its traditional botanical properties in topical or oral formulations.
  • 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 79G1T427CF
    A foaming and cleansing agent derived from coconut oil. It's used in topical products as a thickener and to help create lather or improve how the formula spreads on skin.
  • 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 62V75NI93W
    A surfactant derived from coconut oil that helps cleanse and remove oils from skin or hair. In medicines and personal care products, it acts as a cleanser and foaming agent.
  • UNII 205Z54J075
    A cleansing and conditioning agent derived from coconut oil. It helps reduce static, improve texture, and keep ingredients evenly mixed in shampoos, conditioners, and other personal care products.
  • 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 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 343C7U75XW
    Dimethiconol is a silicone-based fluid that acts as an anti-foaming agent and lubricant in medications. It reduces bubble formation during manufacturing and helps the medicine flow smoothly through equipment.
  • 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 NS34DF43ZK
    A fungal extract from a dark mushroom species used as a natural supplement ingredient. It may function as a flavor or bioactive component in formulations.
  • UNII C5529G5JPQ
    Ginger is a plant-derived ingredient used as a flavoring agent to add taste and aroma to medicines. It may also provide mild soothing properties to support product palatability.
  • 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 0WT12SX38S
    Glycolic acid is an alpha-hydroxy acid derived from sugar cane that helps dissolve and remove dead skin cells. In topical medicines, it works as an exfoliant and pH adjuster to improve skin penetration and product effectiveness.
  • 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 P62Y550X24
    A plant extract from helichrysum flowers that may be used as a natural fragrance, flavor enhancer, or colorant in medicines. It contributes aroma or taste to make the medication more pleasant.
  • 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 H1109Z9J4N
    A natural emulsifier derived from soybean oil. It helps mix oil and water-based ingredients together, ensuring even distribution of active ingredients throughout the medicine.
  • UNII G1L3HT4CMH
    A synthetic compound used in medicines as a preservative and antimicrobial agent. It helps prevent bacterial and fungal growth, extending the product's shelf life.
  • UNII T4V6TWG28D
    A plant-derived thickening agent made from cellulose. It increases viscosity and helps form a gel or paste consistency in medications, and may serve as a binder or coating material in various formulations.
  • UNII 7IFM8431X3
    A fungal extract from a tree-growing mushroom species, used as a natural ingredient to support texture, stability, or bioavailability in the formulation.
  • UNII N72LMW566G
    A synthetic cleansing agent derived from lauryl alcohol and ethylene oxide. It helps dissolve and mix oil and water-based ingredients in liquid medicines, acting as an emulsifier and solubilizer.
  • UNII 178A96NLP2
    Lauryl alcohol is a fatty alcohol derived from natural oils or made synthetically. It acts as an emulsifier and thickener in medicines, helping blend oil and water-based ingredients and giving the product a smooth, creamy texture.
  • 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 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 70J7AE40YN
    A beneficial live bacterium strain added to support the product's probiotic function. It serves as the active microbial component designed to survive in the digestive system.
  • 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 7QQ1EE6RCP
    A synthetic compound made from menthone and glycerin, used in medicines as a flavoring agent and fragrance ingredient. It provides a cooling or minty taste and aroma to make medications more pleasant to take.
  • UNII 033456LFG1
    A plant extract from the root of the black mulberry tree, used as a natural flavoring agent or coloring ingredient to enhance the taste or appearance of the medicine.
  • UNII 4LVZ0Z0ITT
    A plant seed ingredient used as a natural flavoring agent and filler. It adds taste and helps give the medicine its structure and volume.
  • UNII MJ95C3OH47
    A plant extract from olive leaves used in formulations as an antioxidant and preservative. It helps protect the medicine from degradation and extend shelf life.
  • UNII 79K39JU7RN
    A synthetic compound derived from oleic acid that acts as an emulsifier and surfactant. It helps mix oil and water-based ingredients together and improves how the medicine spreads or is absorbed.
  • UNII 5DHE01JX1V
    A synthetic surfactant derived from oleic acid and ethylene oxide. It helps dissolve or disperse oils and other hard-to-mix ingredients in liquid medicines, improving uniformity and stability.
  • UNII 8Q1GYP08KU
    A fungus that grows on caterpillars in high-altitude regions, used in traditional medicine formulations. It may serve as an active botanical ingredient rather than a typical inactive excipient.
  • UNII CUQ3A77YXI
    Panax ginseng root is a plant extract traditionally used in herbal preparations. In medications, it may serve as an active botanical ingredient or be included for flavoring and as a natural preservative or binder in formulations.
  • 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 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 C29NCR5LBE
    A synthetic compound used as an emulsifier and surfactant in medicines. It helps mix oil and water-based ingredients together and improves how the product spreads or flows.
  • UNII YM64C2P6UX
    Rhein is a naturally occurring compound from plants in the rhubarb and senna families. In medicines, it acts as a coloring agent and may help the body absorb or process other ingredients more effectively.
  • UNII 8LLD82AE3S
    A naturally derived sweetener and prebiotic carbohydrate extracted from sugar cane stems. It sweetens the medicine, improves taste, and may help with texture and stability in the formulation.
  • 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 QU52J3A5B3
    A plant extract from black willow bark used as a natural flavoring agent and to add medicinal plant material to the formulation. It may also help preserve the product.
  • UNII 7J95K7ID2S
    A plant extract from the roots of Chinese skullcap, used as a natural coloring agent and to add mild flavor to medicines. It may also help preserve the product's stability.
  • UNII 7Y1255HVXR
    A plant-derived oil from sesame seeds used as an emollient and solvent in topical formulations. It helps distribute active ingredients evenly and keeps products from drying out.
  • 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 1Q73Q2JULR
    Sodium citrate is a salt derived from citric acid. It works as a buffer to maintain the medicine's pH level and may also help improve taste or act as a preservative in the formulation.
  • 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 NCX1UU2D33
    Sodium lauroyl glutamate is a mild cleanser derived from coconut oil and the amino acid glutamate. In medicines, it acts as a surfactant and emulsifier to help mix oily and watery ingredients and improve how the product spreads or dissolves.
  • UNII 632GS99618
    Sodium lauroyl sarcosinate is a mild, plant-derived cleaning agent used in medicines as a surfactant and emulsifier. It helps mix oil and water-based ingredients and may aid tablet disintegration.
  • 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 0YPR65R21J
    Sodium sulfate is a mineral salt used in pharmaceuticals as a filler and diluent. It helps provide bulk and stability to tablets and capsules while remaining inert in the body.
  • 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 8HM7ZD48HN
    A synthetic surfactant made from tea (triethanolamine) and a long-chain organic compound. It reduces surface tension to help distribute and dissolve active ingredients evenly throughout the medicine.
  • UNII Q04E1F5351
    A plant-derived ingredient from the Vitex trifolia fruit. In medicines, it may serve as a natural flavoring, coloring agent, or botanical extract component to support the product's formulation or taste profile.
  • 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 44FQ49X6UN
    A polysaccharide (complex carbohydrate) derived from yeast cell walls. In medicines, it acts as a binder to hold tablet ingredients together and may help with tablet structure and stability.
  • 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.

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

The official label also statesBIFIDA FERMENT FILTRATE,WATER,SODIUM LAURETH SULFATE. GLYCERIN,FRAGRANCE,COCAMIDE METHYL MEA,AMMONIUM LAURYL SULFATE,COCAMIDOPROPYL HYDROXYSULTAINE,DI- METHICONOL,BIFIDA FERMENT LYSATE,PHENOXYETHANOL,SO- DIUM BENZOATE,CITRIC ACID,SODIUM LAUROYL SARCOSINATE, ALLANTOIN,SODIUM CHLORIDE,GUAR HYDROXYPROPYLTRIMO- NIUM CHLORIDE,GLYCOLIPIDS,CARBOMER,DIMETHICONE, 1,2-HEXANEDIOL,SODIUM CITRATE,MENTHOLUM,HYDROXYACE- TOPHENONE,COCAMIDOPROPYL PG-DIMONIUM CHLORIDE,CO- CAMIDOPROPYL BETAINE,SALICYLIC ACID,SODIUM LAURYL SULFATE,PROPYLENE GLYCOL,BRASSICAMIDOPROPYL DIMETHYLAMINE,QUATERNIUM-80,HYDROGENATED CASTOR OIL,AMODIMETHICONE,MENTHONE GLYCERIN ACETAL,OLETH-8,- MENTHOL,COLLOIDAL SULFUR,ZINC PCA,LAURETH-23,TEA-DO- DECYLBENZENESULFONATE,STARCH HYDROXYPROPYLTRIMONI- UM CHLORIDE,SODIUM LAUROYL GLUTAMATE,ETHYLHEXYLGLYC- ERIN,SODIUM SULFATE,DICHLOROBENZYL ALCOHOL,LAURYL ALCOHOL,ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT,BIS- ABOLOL,PIROCTONE OLAMINE,PHYLLOSTACHYS BAMBUSOIDES EXTRACT,BUTYLENE GLYCOL,HYDROGENATED LECITHIN,LACTO- COCCUS FERMENT EXTRACT,LACTOCOCCUS FERMENT LYSATE,FOMES OFFICINALIS (MUSHROOM)EXTRACT,PROPANEDI OL,CENTELLA ASIATICA LEAF EXTRACT,LACTOCOCCUS FERMENT,VITEX TRIFOLIA FRUIT EXTRACT,THUJA ORIENTALIS LEAF EXTRACT,PANAX GINSENG EXTRACT,NIGELLA SATIVA SEED EXTRACT,LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, ZINGIBER OFFICINALE (GINGER) EXTRACT,SESAMUM INDICUM (SESAME) EXTRACT,MORUS NIGRA ROOT EXTRACT,SALIX NIGRA (WILLOW) BARK EXTRACT,GANODERMAATRUM (MUSHROOM) EXTRACT,POLYGONUM MULTIFLORUM EXTRACT,BIOSACCHARIDE GUM-1,FRUCTOOLIGOSACCHARIDES,BETA-GLUCAN,CAPRYLHY- DROXAMIC ACID,OLEA EUROPAEA (OLIVE) LEAF EXTRACT,SCUTE- LLARIA BAICALENSIS ROOT EXTRACT,CORDYCEPS SINENSIS EXTRACT,HELICHRYSUM ITALICUM EXTRACT,HYDROXYETHYLCEL- LULOSE

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

LabelerQingyuan Moksha Biotechnology Co., Ltd.
FDA applicationM032 (OTC MONOGRAPH DRUG)
Labeler code85004
First marketedMar 2026
Product typeHuman Otc Drug
Portfolio2 products on file

More NDCs from Qingyuan Moksha Biotechnology Co., Ltd. labeler code 85004

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use Uses:fights and helps prevent recurrence ofscalp flaking and itching associated with dandruff.

⏱️ Dosage and Administration 33 words ▾

Directions Directions:for best results, use at least twice a week or as directed by a doctor. wet hair and apply small amount of shampoo and massage' onto scalp. rinse and repeat if desired.

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 13 words ▾

Other information Keep container tightly closed and store in a cool, dry,well-ventilated area.

🧪 Active Ingredient 5 words ▾

Active Ingredient(s) SELENIUM DISULPHIDE 1%

🧪 Inactive Ingredients 125 words ▾

Inactive ingredients BIFIDA FERMENT FILTRATE,WATER,SODIUM LAURETH SULFATE. GLYCERIN,FRAGRANCE,COCAMIDE METHYL MEA,AMMONIUM LAURYL SULFATE,COCAMIDOPROPYL HYDROXYSULTAINE,DI- METHICONOL,BIFIDA FERMENT LYSATE,PHENOXYETHANOL,SO- DIUM BENZOATE,CITRIC ACID,SODIUM LAUROYL SARCOSINATE, ALLANTOIN,SODIUM CHLORIDE,GUAR HYDROXYPROPYLTRIMO- NIUM CHLORIDE,GLYCOLIPIDS,CARBOMER,DIMETHICONE, 1,2-HEXANEDIOL,SODIUM CITRATE,MENTHOLUM,HYDROXYACE- TOPHENONE,COCAMIDOPROPYL PG-DIMONIUM CHLORIDE,CO- CAMIDOPROPYL BETAINE,SALICYLIC ACID,SODIUM LAURYL SULFATE,PROPYLENE GLYCOL,BRASSICAMIDOPROPYL DIMETHYLAMINE,QUATERNIUM-80,HYDROGENATED CASTOR OIL,AMODIMETHICONE,MENTHONE GLYCERIN ACETAL,OLETH-8,- MENTHOL,COLLOIDAL SULFUR,ZINC PCA,LAURETH-23,TEA-DO- DECYLBENZENESULFONATE,STARCH HYDROXYPROPYLTRIMONI- UM CHLORIDE,SODIUM LAUROYL GLUTAMATE,ETHYLHEXYLGLYC- ERIN,SODIUM SULFATE,DICHLOROBENZYL ALCOHOL,LAURYL ALCOHOL,ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT,BIS- ABOLOL,PIROCTONE OLAMINE,PHYLLOSTACHYS BAMBUSOIDES EXTRACT,BUTYLENE GLYCOL,HYDROGENATED LECITHIN,LACTO- COCCUS FERMENT EXTRACT,LACTOCOCCUS FERMENT LYSATE,FOMES OFFICINALIS (MUSHROOM)EXTRACT,PROPANEDI OL,CENTELLA ASIATICA LEAF EXTRACT,LACTOCOCCUS FERMENT,VITEX TRIFOLIA FRUIT EXTRACT,THUJA ORIENTALIS LEAF EXTRACT,PANAX GINSENG EXTRACT,NIGELLA SATIVA SEED EXTRACT,LEUCONOSTOC/RADISH ROOT FERMENT FILTRATE, ZINGIBER OFFICINALE (GINGER) EXTRACT,SESAMUM INDICUM (SESAME) EXTRACT,MORUS NIGRA ROOT EXTRACT,SALIX NIGRA (WILLOW) BARK EXTRACT,GANODERMAATRUM (MUSHROOM) EXTRACT,POLYGONUM MULTIFLORUM EXTRACT,BIOSACCHARIDE GUM-1,FRUCTOOLIGOSACCHARIDES,BETA-GLUCAN,CAPRYLHY- DROXAMIC ACID,OLEA EUROPAEA (OLIVE) LEAF EXTRACT,SCUTE- LLARIA BAICALENSIS ROOT EXTRACT,CORDYCEPS SINENSIS EXTRACT,HELICHRYSUM ITALICUM EXTRACT,HYDROXYETHYLCEL- LULOSE

🎯 Purpose 2 words ▾

Purpose Anti-dandruff

📄 Do Not Use 6 words ▾

Do not use OPEN SKIN WOUND

📄 When Using This Product 17 words ▾

When using this product avoid contact with the eyes. lf contact occurs, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 21 words ▾

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 17 words ▾

Keep out of reach of children.If swallowed, get medical help or contact a Poison Control Centerright away.

📄 Package Label / Principal Display Panel 7 words ▾

Package Label - Principal Display Panel undefined

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 Qingyuan Moksha Biotechnology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Qingyuan Moksha 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.
← 85004-0001-01 · Qingyuan 85006-1754-01 · Valorum →
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.