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MQUPIN Liquid Fungal Nail Treatment 1 g/100mL; 1 g/100mL Liquid, 15 mL — NDC 83781-0009-01 package photo

MQUPIN Liquid Fungal Nail Treatment 1 g/100mL; 1 g/100mL Liquid, 15 mL

by Zhengzhou Miaoqi Medical Technology Co., Ltd. · 15 mL in 1 BOTTLE (83781-009-01)
NDC 83781-0009-01
🏷️ FDA NDC (as labeled) 83781-009-01 billing pads the product segment with a zero
This package
Contains15 mL Pack sizes2 compare ↓
Also comes in: 30 ml 83781-0009-02
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) 83781-009-01
Product NDC 83781-009
11-digit billing NDC 83781000901
UNII O414PZ4LPZ, 5908ZUF22Y
UPC 6973634831057
Application # M005
SPL Set ID 14782f8c-3b29-1d88-e063-6294a90ac3e4
Physiologic effect Decreased Cell Wall Integrity
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-03-25
Route TOPICAL
Dosage form LIQUID
Substance SALICYLIC ACID; CHLORHEXIDINE ACETATE
Why two NDCs? The FDA registers this code as 83781-009-01 — 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 → 83781-0009-01. 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

LabelerZhengzhou Miaoqi Medical Technology Co., Ltd.
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code83781
First marketedMar 2024
Product typeHuman Otc Drug
Portfolio10 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?

MQUPIN Liquid Fungal Nail Treatment is a topical liquid product sold over the counter under FDA's OTC monograph rules for antifungal and keratolytic agents. It contains chlorhexidine acetate, an antimicrobial agent typically used to reduce bacteria and fungi on skin, and salicylic acid, a keratolytic that is commonly used to soften and help remove thickened or damaged nail tissue. Together, these ingredients are meant to be applied directly to nails that may be affected by fungal infection.

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 9M69B50875
    A plant extract from angelica dahurica seeds, used in traditional medicine preparations. It may function as a flavoring agent, fragrance component, or botanical extract in formulations.
  • 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 LA97176ILS
    A plant-derived ingredient from the root bark of Dictamnus dasycarpus. It may function as a natural extract or traditional ingredient to support formulation stability or consistency in herbal preparations.
  • 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 3169PS5TJH
    A plant extract from impatiens flowers used as a natural colorant or pigment in medications. It may provide color to tablets or liquids while serving as a botanical ingredient in formulations.
  • UNII 6YZ9PR87NU
    A protein derived from hair or animal tissue that serves as a binder and structural agent in solid dosage forms, helping hold tablet or capsule ingredients together while maintaining the medicine's shape and integrity.
  • UNII A2I8C7HI9T
    Methylparaben is a preservative derived from benzoic acid that prevents growth of bacteria, fungi, and mold in medicines. It extends the product's shelf life and maintains safety during storage.
  • UNII IQC2WQS369
    A plant extract from Panax notoginseng (also called Notoginseng ginseng) used in traditional herbal formulations. It may serve as an active botanical ingredient or natural flavoring component in the medicine.
  • UNII PBG27B754G
    Phellodendron amurense bark is a plant-derived ingredient from the cork tree. It functions as a natural preservative and antimicrobial agent to help maintain product stability and prevent microbial growth.
  • UNII 1BEM3U6LQQ
    A plant extract from rehmannia root, traditionally used in herbal medicine. In pharmaceutical products, it may serve as an active botanical ingredient or functional additive, though its specific role depends on the formulation type.
  • UNII 205MXS71H7
    A plant extract from white willow bark. It's used as a natural flavoring agent and may help preserve the medicine by providing mild antioxidant properties in the formulation.
  • UNII IYR6K8KQ5K
    A plant extract from sophora flavescens root used as a natural colorant and flavoring agent in medicines. It may also help preserve the product and provide texture.
  • 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.
  • UNII TTV12P4NEE
    Xanthan gum is a thickening and stabilizing ingredient made from fermented corn or other sugars. It's added to medicines to improve texture, prevent separation of liquids and solids, and help the product stay consistent.

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

The official label also statesWater, Glycerin, Xanthan Gum, Rehmannia Chinensis Root Extract, Sophora Flavescent Root Extract, Alix Alba (Willow) Bark Extract, Tea Tree Essential Oil Extract, Keratin, Impatiens Balsamina Flower Extract, Dictamnus Dasycarpus Root Bark Extract, Extract Of Panax Notoginseng, Angelica dahurica, Phellodendron Bark Extract, Methylparaben, Caprylhydrpxamic Acid

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

Inactive ingredient FAQ

Are inactive ingredients the same for every manufacturer?
No. Inactive ingredients can differ by manufacturer, dosage form, strength, and package / product version.
Why might an inactive ingredient be missing?
Some SPLs do not provide a complete structured inactive-ingredient list, and older or unusual labels may only include the information in narrative text.
Can inactive ingredients matter?
Yes. They can matter for allergies, intolerances, dyes, gluten / lactose concerns, preservatives, and formulation differences — but confirm with a pharmacist or the manufacturer when it’s clinically important.

💲 Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 30 ml
Where does this data come from?
NADAC (National Average Drug Acquisition Cost) is the CMS weekly pharmacy-acquisition-cost survey — what pharmacies pay. ASP (Average Sales Price) is the CMS Medicare Part B drug-payment file, published quarterly. Medicaid pays is computed by us from CMS State Drug Utilization Data (total reimbursed ÷ units, trailing 12 months) — gross of rebates and inclusive of dispensing fees, so it reflects what Medicaid paid, not an acquisition cost. Medicare drug plans pay is the median negotiated point-of-sale unit cost across plans listing this NDC in the CMS quarterly Prescription Drug Plan pricing files, before rebates. The VA pays is the federal contract price (FSS, and the statutory Big 4 ceiling where listed) from the VA National Acquisition Center pharmaceutical price file. All are free public government data; each measures a different payer, so the figures are not directly comparable.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MQUPIN Liquid Fungal Nail Treatment 1 g/100mL; 1 g/100mLthis 83781-0009-01 Zhengzhou 15 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

🏛️
2024
On the market since
Mar 2024
📍
2026
Currently FDA-listed
2 years 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
83781-0009-01 You're viewing this 15 mL in 1 BOTTLE (83781-009-01) 2024-03-25 Active
83781-0009-02 30 mL in 1 BOTTLE (83781-009-02) 2024-03-25 Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 83781-0009-01?
NDC 83781-0009-01 contains 15 mL — 15 ml in 1 bottle.
What is the difference between NDC 83781-0009-01 and NDC 83781-0009-02?
Both are MQUPIN Liquid Fungal Nail Treatment 1 g/100mL; 1 g/100mL Liquid — the drug itself is identical. NDC 83781-0009-01 is the 15 mL package, while NDC 83781-0009-02 is the 30 ml package.
What NDC number is used to bill for this package of MQUPIN Liquid Fungal Nail Treatment 1 g/100mL; 1 g/100mL Liquid?
Bill NDC 83781-0009-01 — the 11-digit billing format is 83781000901. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 About this NDC listing & data coverage

Over-the-counter (OTC) product
What data is (and isn’t) available for this NDC — tap to expand
NDC identity (package / product / labeler codes) ✓ Available
Labeler ✓ Available
Product & package description ✓ Available
Marketing category & status ✓ Available
Active ingredient / dosage form / route ✓ Available
FDA label (SPL via DailyMed) ✓ Available
Package photos ✓ Available
Inactive ingredients (structured) ✓ Available
NADAC pharmacy acquisition price (CMS) — Not published for this NDC CMS publishes NADAC only for NDCs reported in its retail-pharmacy survey.
Orange Book / therapeutic-equivalence data — Not published for this NDC Applies only to products approved under an NDA/ANDA; many listings are out of scope.
HCPCS J-code billing crosswalk — Not published for this NDC Most self-administered / retail products have no J-code — that is normal.
Medicaid utilization (CMS SDUD) — Not published for this NDC CMS reports utilization only for NDCs with Medicaid claims above its privacy threshold.
“Not published” reflects what the public FDA / CMS / NLM sources provide for this exact package code — it is a property of the data feeds, not a judgment about the product.

Questions about this listing

Is this NDC FDA-approved?
An NDC listing does not by itself establish FDA approval — the NDC Directory records that a product is listed with FDA, not that it was reviewed and approved. This listing's marketing category is "Otc Monograph Drug". Products approved under an application carry an NDA, ANDA, or BLA number.
Why is there no price listed?
The pricing shown on our NDC pages comes from CMS NADAC, a voluntary survey of retail community pharmacy invoices. CMS does not publish a NADAC for every NDC — packages outside the retail survey (institutional and hospital products, bulk packages, discontinued items, and many OTC items) may never receive one. A missing price reflects the survey's scope, not this product's actual cost, and does not mean the product is free or unavailable.
Is the NDC printed on the package the same as the 11-digit billing NDC?
Yes, they identify this exact package in different formats. The FDA registers it as 83781-009-01, 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: 83781-0009-01, written without dashes as 83781000901. 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 83781-0009-01, the first segment (83781) is the labeler code FDA assigned to Zhengzhou Miaoqi Medical Technology Co., Ltd.; the middle segment (0009) 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 Zhengzhou Miaoqi Medical Technology Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 30 ml (83781-0009-02). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Zhengzhou Miaoqi Medical Technology 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose
🎯 Indications and Usage 10 words ▾

Use Helpful eliminate the fungus and promote healthier nail growth.

⏱️ Dosage and Administration 83 words ▾

Directions ■Wash your hands & feet Before Use. ■Use your nail file to repair the nail scrape of te dirt & make it thinner. ■Apply a thin layer of liquid using the nail brush onto the affected area. ■Repeat this process 2-3 times daily until a healthy nail begins regenerating, and for best results, continue use for 6 weeks straight. ■The Toenail Fungus Treatment demonstrates visible improvements in just 4-5 weeks, effectively addressing brittle and compromised nails within a span of 3 months.

⚠️ Warnings 5 words ▾

Warnings For external use only.

📦 Storage and Handling 19 words ▾

Other information ■Store at room temperature and out of direct sunlight ■Skin discoloration may occur during or after use.

🧪 Active Ingredient 8 words ▾

Active Ingredient Chlorhexidine Diacetate 1% Salicylic Acid 1%

🧪 Inactive Ingredients 46 words ▾

Inactive ingredients Water, Glycerin, Xanthan Gum, Rehmannia Chinensis Root Extract, Sophora Flavescent Root Extract, Alix Alba (Willow) Bark Extract, Tea Tree Essential Oil Extract, Keratin, Impatiens Balsamina Flower Extract, Dictamnus Dasycarpus Root Bark Extract, Extract Of Panax Notoginseng, Angelica dahurica, Phellodendron Bark Extract, Methylparaben, Caprylhydrpxamic Acid

🎯 Purpose 2 words ▾

Purpose Anti-Fungal

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83781-0008-01 · Zhengzhou 83781-0010-01 · Zhengzhou →
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.