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Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001 Patch, 6 patches — NDC 83559-0023-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001 Patch, 6 patches — NDC 83559-023-01 (Billing 83559-0023-01)

by Henan Enokon Medical Instrument Co., Ltd. · 6 BAG in 1 BOX / 1 PATCH in 1 BAG

This is a package of 6 patches of Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001 Patch from Henan Enokon Medical Instrument Co., Ltd., marketed since Sep 2026 and currently FDA-listed. It is the main listing for this product, which comes in 7 package sizes.

NDC 83559-0023-01
🏷️ FDA NDC (as labeled) 83559-023-01 billing pads the product segment with a zero
This package
Contains6 patches Pack sizes7 compare ↓
Main listing for product 83559-023 · Also comes in: 8 patches 83559-023-02 10 patches 83559-023-03 12 patches 83559-023-04 20 patches 83559-023-05 24 patches 83559-023-06 30 patches 83559-023-07
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Sep 17, 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 83559-023-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
83559 labeler · 023 product · 01 package
Package marketed since
Sep 1, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 8355902301 1
FDA record last changed
Sep 17, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 83559-023-01
Product NDC 83559-023
11-digit billing NDC 83559002301
RxCUI 1249758
UNII 98PI200987, L7T10EIP3A
Application # M017
SPL Set ID 5a68fe67-5c15-af9a-e063-6294a90a7ec1
Established class (EPC) Amide Local Anesthetic; Antiarrhythmic
Physiologic effect Local Anesthesia
Chemical class Amides
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-09-01
Route TOPICAL
Dosage form PATCH
Substance LIDOCAINE; MENTHOL
Quick answers
  • RxCUI (RxNorm): 1249758
Why two NDCs? The FDA registers this code as 83559-023-01 — 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 → 83559-0023-01. 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 Antiarrhythmic class.

Pharmacologic class Antiarrhythmic, Amide Local Anesthetic
Drug family (ATC) Antiarrhythmics, class Ib, Local anesthetics, Anesthetics 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 is this product?

Gaimoa Lidocaine Pain Relief Gel Patches is a topical patch product marketed as an over-the-counter monograph drug. It contains lidocaine and menthol as active ingredients. Lidocaine is a local anesthetic typically used to numb pain at the skin surface, while menthol is commonly used for its cooling sensation to provide temporary relief of minor aches and discomfort. The patch is applied directly to the skin over the area where pain relief is desired.

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 eachPer 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: 8 patches 10 patches 12 patches 20 patches 24 patches 30 patches
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
83559-0023-01 You're viewing this Main listing 6 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-02 83559-023-02 8 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-03 83559-023-03 10 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-04 83559-023-04 12 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-05 83559-023-05 20 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-06 83559-023-06 24 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active
83559-0023-07 83559-023-07 30 BAG in 1 BOX / 1 PATCH in 1 BAG 2026-09-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 6 patches — 6 bag in 1 box / 1 patch in 1 bag.
How does this package differ from NDC 83559-0023-02?
Both are Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001 Patch — the drug itself is identical. This page's package is the 6 patches one, while NDC 83559-0023-02 is the 8 patches package.
What NDC number is used to bill for this package of Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001 Patch?
Use the 11-digit billing form listed in the identifiers section of this page. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Gaimoa Lidocaine Pain Relief Gel Patches 4 g/1001; 1 g/1001this 83559-0023-01 Henan 6 patches — — 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
Sep 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.

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

  • UNII 1K713C615K
    A mineral compound of aluminum that acts as an antacid and absorbent in formulations. It helps neutralize stomach acid and is used as a filler or binding agent in solid dosage forms.
  • UNII K679OBS311
    Carboxymethylcellulose sodium is a plant-derived thickening agent made from cellulose. In medicines, it acts as a binder to hold ingredients together, a disintegrant to help the tablet break apart, or a thickener in liquids.
  • UNII 7FLD91C86K
    Edetate disodium is a chemical compound that binds and removes certain metal ions. In medicines, it acts as a preservative and stabilizer by preventing metals like calcium from interfering with the product's shelf life and consistency.
  • 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 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 24H4NWX5CO
    Kaolin is a naturally occurring clay mineral. It's used in tablets and capsules as a filler and absorbent to add bulk, improve texture, and help bind ingredients together.
  • 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 FZ989GH94E
    Povidone is a synthetic polymer made from a plastic-like material. It acts as a binder to hold tablet ingredients together and as a disintegrant to help the tablet break apart in your stomach so the medicine can be absorbed.
  • 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 7C98FKB43H
    Sodium acrylate is a synthetic polymer (plastic-like material) used as a superabsorbent and thickening agent in medicines. It helps control the consistency and release of active ingredients, particularly in gel or semi-solid formulations.
  • UNII W4888I119H
    Tartaric acid is a natural organic acid found in grapes and tamarinds. In medicines, it works as a buffer to control acidity, an antioxidant to prevent spoilage, and sometimes a flavoring or binding agent.
  • 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.

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

The official label also statesAluminum Glycinate, EdetateDisodium, Ethylhexylglycerin, Glycerin, Kaolin, Phenoxyethanol, Polyvinylpyrrolidone, Propylene Glycol, Sodium Carboxymethylcellulose, Sodium Polyacrylate, Tartaric Acid, Water

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

LabelerHenan Enokon Medical Instrument Co., Ltd.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code83559
First marketedSep 2026
Product typeHuman Otc Drug
Portfolio20 products on file

More NDCs from Henan Enokon Medical Instrument Co., Ltd. labeler code 83559

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

Use Temporarily relieves muscle soreness and minor joint pain in the wrist, knees, back,neck, hips, shoulders, and elbows.

⏱️ Dosage and Administration 65 words ▾

Directions Directions Adults and children 12 years of age and over clean and dry affected area 1.remove film from patch and apply to the skin (see illustration) 2.apply 1 patch at a time to affected area, not more than 3 to 4 times daily 3.remove patch from the skin after at most 8 hours of application Children under 12 years of age: Consult a doctor

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 19 words ▾

Other information Other information avoid storing product in direct sunlight protect product from excessive moisture store at 20-25°C (68-77°F)

🧪 Active Ingredient 6 words ▾

Active Ingredient Lidocaine 4% Menthol 1%

🧪 Inactive Ingredients 19 words ▾

Inactive ingredients Aluminum Glycinate, EdetateDisodium, Ethylhexylglycerin, Glycerin, Kaolin, Phenoxyethanol, Polyvinylpyrrolidone, Propylene Glycol, Sodium Carboxymethylcellulose, Sodium Polyacrylate, Tartaric Acid, Water

🎯 Purpose 3 words ▾

Purpose Topical Analgesic

📄 Do Not Use 38 words ▾

Do not use Do not use 1.more than 1 patch at a time 2.on wounds or damaged skin 3.with a heating pad 4.if you have ever had an allergic reaction to this product or any of its ingredients

📄 Ask a Doctor Before Use If 11 words ▾

Ask Doctor Children under 12 years of age: consult a doctor

📄 When Using This Product 23 words ▾

When Using When using this product 1.use only as directed 2.avoid contact with the eyes, mucous membranes or rashes 3.do not bandage tightly

📄 Keep Out of Reach of Children 12 words ▾

Keep Out Of Reach Of Children Keep Out Of Reach Of Children

📄 Package Label / Principal Display Panel 7 words ▾

1 2 3 4 5 6 7

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 Henan Enokon Medical Instrument 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 6 other package presentations of this same product, including 8 patches (83559-0023-02), 10 patches (83559-0023-03), 12 patches (83559-0023-04). 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?
Henan Enokon Medical Instrument 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.
← 83559-0022-01 · Henan 83564-0110-00 · Humacyte →
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.