Home › NDC Lookup › Ingredients › Bee Venom Corn Callus Removers › 83781-0013-02
MQXUNMI BEE VENOM CORN CALLUS REMOVERS 5 g/100mL; 2 g/100mL; 2 g/100mL Liquid, 20 mL — NDC 83781-0013-02 package photo

MQXUNMI BEE VENOM CORN CALLUS REMOVERS 5 g/100mL; 2 g/100mL; 2 g/100mL Liquid, 20 mL

by Zhengzhou Miaoqi Medical Technology Co., Ltd. · 20 mL in 1 BOTTLE (83781-013-02)
NDC 83781-0013-02
🏷️ FDA NDC (as labeled) 83781-013-02 billing pads the product segment with a zero
This package
Contains20 mL Pack sizes3 compare ↓
Also comes in: 15 ml 83781-0013-01 30 ml 83781-0013-03
OTC On market Non-controlled
🗂️ Data synced Aug 27, 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) 83781-013-02
Product NDC 83781-013
11-digit billing NDC 83781001302
UNII Y9H1V576FH, 76013O881M, O414PZ4LPZ
Application # M030
SPL Set ID 41952a0e-2bd2-db3c-e063-6294a90a4a79
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-10-20
Route TOPICAL
Dosage form LIQUID
Substance HONEY; APIS MELLIFERA VENOM; SALICYLIC ACID
Why two NDCs? The FDA registers this code as 83781-013-02 — 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 → 83781-0013-02. 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 applicationM030 (OTC MONOGRAPH DRUG)
Labeler code83781
First marketedOct 2025
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?

This is a topical liquid product marketed as an over-the-counter monograph drug for corn and callus removal. It contains salicylic acid, which is typically used to soften and help remove thickened skin, along with honey and bee venom. Honey is commonly included in skincare products for its moisturizing properties, while bee venom appears in various topical formulations. The product is applied directly to the affected skin area.

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 Q40Q9N063P
    Acetic acid is a weak organic acid commonly used in medicines as a buffer and pH adjuster. It helps maintain the proper acidity level to ensure the drug remains stable and effective in its formulation.
  • UNII 636VYW51FP
    Plant extract from Canadian columbine flower. Used as a natural coloring agent or flavoring component in some formulations to provide color or taste to the medicine.
  • UNII V1IA3S3CUS
    A plant extract derived from Cnidium monnieri fruit, commonly used in traditional Asian medicine preparations. In formulations, it may serve as an active botanical ingredient or flavoring agent, though its specific role depends on the product type.
  • UNII 65ER808MP7
    A plant extract from hawthorn fruit used as a natural flavoring and coloring agent in medicines. It may also help bind ingredients together in tablet or capsule formulations.
  • UNII 14R2W5JO8E
    A protein extracted from a marine snail (keyhole limpet) that carries oxygen in its blood. In medicines, it's used as an immune-stimulating ingredient to help activate the body's defense response in certain vaccine or immunotherapy formulations.
  • 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 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.

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

The official label also statesAqua, Glacial Acetic Acid, Hawthorn seed extract, Frutus cnidii, Kuh-seng, Honeysuckle, Propylene glycol.

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: 15 ml 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
Mqxunmi Bee Venom Corn Callus Removers 5 g/100mL; 2 g/100mL; 2 g/100mLthis 83781-0013-02 Zhengzhou 20 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
Oct 2025
📍
2026
Currently FDA-listed
1 year listed
🔒
·
No generic listed yet
brand only
ℹ️No FDA-approved generic found

We did not find an FDA-approved generic match for this exact strength, form and route.

Where does this data come from?
Patents and exclusivity from the FDA Orange Book (small-molecule drugs), refreshed from public FDA data. Generic launch timing is an estimate, not a guarantee.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
83781-0013-01 15 mL in 1 BOTTLE (83781-013-01) 2025-10-20 Active
83781-0013-02 You're viewing this 20 mL in 1 BOTTLE (83781-013-02) 2025-10-20 Active
83781-0013-03 30 mL in 1 BOTTLE (83781-013-03) 2025-10-20 Active

You're viewing one of 3 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 83781-0013-02?
NDC 83781-0013-02 contains 20 mL — 20 ml in 1 bottle.
What is the difference between NDC 83781-0013-02 and NDC 83781-0013-01?
Both are MQXUNMI BEE VENOM CORN CALLUS REMOVERS 5 g/100mL; 2 g/100mL; 2 g/100mL Liquid — the drug itself is identical. NDC 83781-0013-02 is the 20 mL package, while NDC 83781-0013-01 is the 15 ml package.
What NDC number is used to bill for this package of MQXUNMI BEE VENOM CORN CALLUS REMOVERS 5 g/100mL; 2 g/100mL; 2 g/100mL Liquid?
Bill NDC 83781-0013-02 — the 11-digit billing format is 83781001302. 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 83781-013-02, 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: 83781-0013-02, written without dashes as 83781001302. 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 83781-0013-02, the first segment (83781) is the labeler code FDA assigned to Zhengzhou Miaoqi Medical Technology Co., Ltd.; the middle segment (0013) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 2 other package presentations of this same product, including 15 ml (83781-0013-01), 30 ml (83781-0013-03). 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 16 words ▾

Use For the corn and callus areas on the feet and hands (avoid face or genitals).

⏱️ Dosage and Administration 97 words ▾

Directions 1.Wash the corn & callus area with water and dry the skin. 2.Unscrew the cap to open. Dip the liquid with the brush and apply it on the affected area.

Wait in minutes after the liquid dries and turn to mask and apply one more time. 3.Repeat the above process twice a day, morning and evening. If the issue is foot - based, apply before bedtime to minimize friction.

4.Continue daily application for at least 2 weeks until the skin appears smooth. More severe cases may require more time. Remain patient and consistent during the application.

⚠️ Warnings 18 words ▾

Warnings For external use only. Keep out of children's reach. Avoid eye contact; rinse with water if needed.

📦 Storage and Handling 18 words ▾

Other information Keep bottle tightly closed. Store at 15°C-30°C (59°F-86°F). Protect from heat and sunlight. Do not freeze.

🧪 Active Ingredient 9 words ▾

Active Ingredient Salicylic Acid.......2% Bee venom extract......2% Honey extract......5%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients Aqua, Glacial Acetic Acid, Hawthorn seed extract, Frutus cnidii, Kuh-seng, Honeysuckle, Propylene glycol.

🎯 Purpose 4 words ▾

Purpose Corn, Callus Remover

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 83781-0012-01 · Zhengzhou 83781-0014-01 · 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.