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NEOMEN Nail Repair Pen Nail repair pen liquid 10 g/100mL Liquid, 3 mL — NDC 83887-006-01 (Billing 83887-0006-01)

by Changsha Beiliang E-commerce Co., Ltd · 3 mL in 1 TUBE

This is a package of 3 mL of NEOMEN Nail Repair Pen Nail repair pen liquid 10 g/100mL Liquid from Changsha Beiliang E-commerce Co., Ltd, no longer marketed (first marketed Apr 2025), no longer in the FDA NDC Directory. It is this product's only package size.

NDC 83887-0006-01
🏷️ FDA NDC (as labeled) 83887-006-01 billing pads the product segment with a zero
OTC Discontinued Non-controlled ⚠ Inactivated by FDA ⇄ 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 83887-006-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83887 labeler · 006 product · 01 package
Package marketed since
Apr 22, 2025
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8388700601 4
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. FDA inactivated this product’s listing record, so it is excluded from the active NDC Directory. The listing was last certified through Dec 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83887-006-01
Product NDC 83887-006
11-digit billing NDC 83887000601
RxCUI 1251008
UNII K3D86KJ24N
Application # M005
SPL Set ID 3356b681-f499-7d0e-e063-6294a90adaf6
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Inactivated by FDA (certified through Dec 2026)
Marketing start 2025-04-22
Route TOPICAL
Dosage form LIQUID
Substance UNDECYLENIC ACID
Quick answers
  • RxCUI (RxNorm): 1251008
Why two NDCs? The FDA registers this code as 83887-006-01 — 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 → 83887-0006-01. 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

📗 Our plain-language guide HelloPharmacist
  • It treats three common fungal skin infections: athlete's foot (the itchy, scaly condition that affects the feet and toes), jock itch (a fungal rash in the groin area), and ringworm...
  • What exactly does undecylenic acid treat?
  • For athlete's foot and ringworm, most products are used daily for 4 full weeks. For jock itch, 2 weeks of daily use is typically recommended. Some nail products note that visible i...
  • That depends on the product. Most undecylenic acid creams, sprays, and general topical solutions are not effective on nails and should not be used there. However, some products — l...
📖 Read our full Undecylenic 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 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.
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
83887-0006-01 You're viewing this Main listing 3 mL in 1 TUBE 2025-04-22 — Inactivated by FDA

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
EmoniNail Antifungal 100 mg/mL 65121-0071-08 Pure 24 ml — — FDA listed —
EmoniNail Antifungal 100 mg/mL 76973-0071-08 GG 24 ml — — FDA listed —
NEOMEN Nail Repair Pen 10 g/100mLthis 83887-0006-01 Changsha 3 ml — — Discontinued —
Osimoon Fungal Nail Treatment Kit 10 g/100mL 85150-0008-01 Guangzhou 2 bottles — — FDA listed —
BeamBalm ANTIFUNGAL CARE ESSENTIAL Oil 10 g/100mL 85248-0191-01 Jiangxi 10 ml — — FDA listed —
OSIMOON Toenail Fungus Treatment 10 g/100mL 87408-0001-01 Guangzhou 2 bottles — — FDA listed —
Tuymec FUNGAL NAIL TREATMENT Kit 10 g/100mL 87408-0004-01 Guangzhou 2 bottles — — FDA listed —
Osimoon Fungal Nail Renewal 10 g/100mL 87408-0006-01 Guangzhou 2 bottles — — FDA listed —
OSIMOON FUNGAL NAIL TREATMENT Kit 10 g/100mL 87408-0019-01 Guangzhou 2 bottles — — FDA listed —
About this product: other versions of the same ingredient, strength and form are listed above, least expensive first, with FDA equivalence ratings where available.
Where does this data come from?
Equivalents are other NDCs of the same ingredient, form and route from the openFDA NDC Directory, ranked least-expensive-first by NADAC. Therapeutic-equivalence (AB) ratings come from the FDA Orange Book; biologics use the FDA Purple Book for biosimilar & interchangeable status.

Availability & generic status

🏛️
2025
On the market since
Apr 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.

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 Undecylenic 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 1V63N2S972
    A plant extract from angelica dahurica root used in traditional formulations. It may function as a flavoring agent, fragrance component, or natural ingredient to add therapeutic appeal to the medicine.
  • UNII 8SH93A7QWW
    Chitin is a natural polymer derived from shellfish shells and insect exoskeletons. It acts as a binder and thickening agent to help hold tablet ingredients together and improve product texture.
  • 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.

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

The official label also statesDeacetylation Chitin, Salicylic Acid, Angelica Dahurica Root

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

LabelerChangsha Beiliang E-commerce Co., Ltd
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code83887
First marketedApr 2025
Product typeHuman Otc Drug
Portfolio6 products on file

More NDCs from Changsha Beiliang E-commerce Co., Ltd labeler code 83887

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 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 30 words ▾

Use • Improves nail appearance. • For the treatment of fungal infections such as Candida albicans and other fungi, helps relieve symptoms caused by nail fungus, including discoloration and brittleness.

⏱️ Dosage and Administration 68 words ▾

Directions Wash and dry nails before application. Remove the cap covering the brush. Twist the end of the pen clockwise to dispense liquid onto the brush. Using the brush, apply a thin layer of liquid onto the affected area. Let the area dry, then reapply another thin layer. Do this two more times. Repeat this process 3 times daily for 6-8 weeks, or until the infection is gone.

⚠️ Warnings 18 words ▾

Warnings For external use only (for nail fungus/onychomycosis only). This product is not a substitute for prescription medicine.

📦 Storage and Handling 10 words ▾

Other information Store at 20° to 25°C (68° to 77°F).

🧪 Active Ingredient 5 words ▾

Active Ingredient Undecylenic Acid 10%

🧪 Inactive Ingredients 11 words ▾

Inactive ingredients Deacetylation Chitin , Salicylic Acid , Angelica Dahurica Root

🎯 Purpose 2 words ▾

Purpose Antifungal

📄 Do Not Use 29 words ▾

Do not use • On damaged skin (cuts, abrasions, eczema, or sunburn). • If you are allergic to any of the ingredients. • If you are pregnant or breastfeeding.

📄 Ask a Doctor Before Use If 20 words ▾

Ask Doctor You develop symptoms of an allergic reaction (such as itching, rash, swelling of lips, eyelids, or difficulty breathing).

📄 When Using This Product 6 words ▾

When Using Avoid contact with eyes.

📄 Stop Use and Ask a Doctor If 20 words ▾

Stop Use You develop symptoms of an allergic reaction (such as itching, rash, swelling of lips, eyelids, or difficulty breathing).

📄 Keep Out of Reach of Children 12 words ▾

Keep Oot Of Reach Of Children Keep Oot Of Reach Of Children

📄 Questions or Comments 2 words ▾

Questions www.neomenstore.com

📄 Package Label / Principal Display Panel 4 words ▾

PRINCIPAL DISPLAY PANEL 1

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 No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Who lists this product with the FDA?
Changsha Beiliang E-commerce 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.
← 83887-0005-01 · Changsha 83887-0007-01 · Changsha →
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.