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Lidocaine 4% Patch 4 g/100g Patch, 5 pouches — NDC 87236-0024-05 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Lidocaine 4% Patch 4 g/100g Patch, 5 pouches — NDC 87236-024-05 (Billing 87236-0024-05)

by Aldermed Inc. · 5 POUCH in 1 CARTON / 1 g in 1 POUCH

This is a package of 5 pouches of Lidocaine 4% Patch 4 g/100g Patch from Aldermed Inc., marketed since Jul 2026 and currently FDA-listed.

NDC 87236-0024-05
🏷️ FDA NDC (as labeled) 87236-024-05 billing pads the product segment with a zero
This package
Contains5 pouches Pack sizes2 compare ↓
Product page 87236-0024-01 Also comes in: 1 g 87236-024-01
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 20, 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 87236-024-05 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
87236 labeler · 024 product · 05 package
Package marketed since
Jul 22, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0850083488765
FDA record last changed
Aug 20, 2026
⚠️
Other active recalls for Lidocaine (different manufacturers) — 2 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Aug 31, 2026 — Failed Content Uniformity Specifications. Out of Specification for Assay during analysis at the 24- month long term stability station, at (25¿C,60%RH). (SUN PHARMA /TARO) · FDA recall D-0848-2026
Class III · Apr 20, 2023 — Labeling: Typographical error on the upper left-hand side of the box and individual patch label that has the incorrect dosage form stating, each tablet contains instead of each adhesive patch contains. (Bryant Ranch Prepack, Inc.) · FDA recall D-0556-2023
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 87236-024-05
Product NDC 87236-024
11-digit billing NDC 87236002405
RxCUI 1737778
UNII 98PI200987
UPC 0850083488765
Application # M017
SPL Set ID 579a5012-837a-828b-e063-6294a90a4fb2
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 2026-07-01
Route TOPICAL
Dosage form PATCH
Substance LIDOCAINE
Quick answers
  • RxCUI (RxNorm): 1737778
Why two NDCs? The FDA registers this code as 87236-024-05 — 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 → 87236-0024-05. 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 it is MedlinePlus · NLM

Prescription lidocaine transdermal (Dermalid®, Lidoderm®, Ztildo®) is used to relieve the pain of post-herpetic neuralgia (PHN; burning, stabbing pains, or aches that may last for months or years after a shingles infection). Nonprescription (over-the-counter) lidocaine (Absorbine Jr®, Aspercreme®, Lidocare®, Salonpas®, others) is also available to relieve minor pain in shoulders, arms, back, neck and legs in adults and children 12 years of age and older. Lidocaine is in a class of medications called local anesthetics. It works by stopping nerves from sending pain signals.

Read the full MedlinePlus article ↗
📗 Our plain-language guide HelloPharmacist
  • Lidocaine numbs the area where it is used. Clinicians inject it for procedures. Skin products are used for pain, itching, minor burns, insect bites, hemorrhoid discomfort, and in s...
  • Clean and dry the skin first, then apply as your product’s directions say. Wash your hands afterward. Don’t exceed the number of uses on the label. Ask a doctor before using a prod...
  • No. Heat can increase how much lidocaine your body absorbs. Don’t bandage tightly either. Also avoid using other topical pain products at the same time.
  • Can I use a heating pad with a lidocaine patch?
📖 Read our full Lidocaine guide →
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: 1 g
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
87236-0024-01 87236-024-01 Main listing 1 g in 1 POUCH 2026-07-01 — Active
87236-0024-05 You're viewing this 5 POUCH in 1 CARTON / 1 g in 1 POUCH 2026-07-22 — Active

Pack size FAQ

What quantity is in this package?
This package contains 5 pouches — 5 pouch in 1 carton / 1 g in 1 pouch.
How does this package differ from NDC 87236-0024-01?
Both are Lidocaine 4% Patch 4 g/100g Patch — the drug itself is identical. This page's package is the 5 pouches one, while NDC 87236-0024-01 is the 1 g package.
What NDC number is used to bill for this package of Lidocaine 4% Patch 4 g/100g 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
Good Neighbor Pain Relief Patch With Lidocaine 4% 4 g/100g 46122-0820-45 Amerisource 5 patches $1.100 — Availability likely —
Leader PAIN RELIEF PATCHES 4 g/100g 70000-0557-01 Cardinal 6 patches $1.100 — Availability likely —
Quality Choice Lidocaine Pain Relief Patch 4 g/100g 83324-0257-05 Quality 5 patches $1.100 — Availability likely —
Lidocaine Pain Relief 4 g/100g 70000-0740-01 Cardinal 6 patches $1.100 — Availability likely —
Pain Relief Patches 4 g/100g 46122-0450-21 Amerisource 5 patches $1.100 — Availability likely —
Leader PAIN RELIEF PATCHES 4 g/100g 70000-0366-01 Cardinal 5 patches $1.100 — Availability likely —
Rugby PAIN RELIEF PATCHES 4 g/100g 00536-1202-07 RUGBY 30 patches $1.100 — Availability likely —
Lidocaine 4 g/100g 79643-0005-01 PHARMACURE 10 patches — — FDA listed —
Lidocaine 4 g/100g 79643-0008-01 PHARMACURE 10 patches — — FDA listed —
DRMITSUI Lidocaine 4% Pain Relieving Gel 4 g/100g 85713-0102-01 Guangzhou 6 patches — — Discontinued —
Rite Aid Lidocaine Patch XLarge 4 g/100g 11822-9992-03 Rite 3 pouches — — FDA listed —
Lidocaine Pain Relief 4 g/100g 70000-0741-01 Cardinal 5 patches — — FDA listed —
TheraCare Pain Relief Lidocaine 4 g/100g 71101-0011-05 Veridian 5 patches — — FDA listed —
Lido King Lidocaine 4% Pain Relieving Gel-Patch 4 g/100g 73354-1280-02 Galaxy 5 patches — — FDA listed —
Meijer Lidocaine Pain Relief Back And Large Areas 4 g/100g 79481-0021-06 Meijer 1 patch — — FDA listed —
Lidocanna 4 g/100g 79643-0001-01 PHARMACURE 10 patches — — FDA listed —
Pain Patch Perfecto 24 Hours Lidocaine 4 % Patch 4 g/100g 83184-0221-01 Painpatchperfecto 6 patches — — FDA listed —
Maximum Strength Pain Relief Lidocaine Patch 4 g/100g 11822-6541-00 Rite 6 patches — — FDA listed —
Kroger Pain Relief Lidocaine Patch 4 g/100g 30142-0583-06 Kroger 6 patches — — FDA listed —
Pain Relief Patches 4 g/100g 60000-0911-05 Ahold 5 patches — — FDA listed —
Lidocaine 4 Percent 4 g/100g 68788-4123-01 Preferred 10 patches — — FDA listed —
Pain Relief Patches 4 g/100g 00363-9110-05 Walgreen 5 patches — — FDA listed —
Lidocaine 4 Percent 4 g/100g 71436-3104-01 ARI 10 patches — — FDA listed —
else. 4 g/100g 85981-0001-05 Else 5 patches — — FDA listed —
Aspercreme with Lidocaine 4 g/100g 41167-0584-00 Chattem, 5 patches — — FDA listed —
Meijer Pain Relief Patches 4 g/100g 41250-0972-05 Meijer 5 patches — — FDA listed —
Lidocaine 4% Maximum OTC Strength 4 g/100g 55154-7813-05 Cardinal 5 patches — — FDA listed —
Curist Lidocaine Maximum Strength 4 g/100g 72559-0016-19 Little 20 patches — — Discontinued —
Curist Lidocaine Patch Maximum Strength 4 g/100g 72559-0025-19 Little 20 patches — — FDA listed —
Pain Relief Patch Lidocaine 4 g/100g 42507-0960-06 HyVee 6 pouches — — FDA listed —
TheraCare Pain Relieving Patch with Lidocaine 4 g/100g 71101-0918-12 Veridian 1 g — — FDA listed —
Meijer Lidocaine Pain Relief Patch Assortment Medium 4 g/100g 79481-0004-02 Meijer 1 patch — — FDA listed —
Albertsons Pain Relief Patch 4 g/100g 21130-0960-06 Safeway 6 patches — — FDA listed —
Discount Drug Mart Pain Relief Patches 4 g/100g 53943-0911-05 Discount 5 patches — — FDA listed —
TheraCare Flexible Pain Relieving 4 g/100g 71101-0124-01 Veridian 7 patches — — FDA listed —
Honest Med Lidocaine Pain Relief Patch 4 g/100g 84097-0001-30 Proper 30 patches — — FDA listed —
Flanax Back Pain Relief 4 g/100g 27854-0311-01 Belmora 1 patch — — FDA listed —
OTC Rescue Lidocaine Pain Relief Patch 4 g/100g 71101-0025-30 Veridian 30 patches — — FDA listed —
Pain Relief Patches 4 g/100g 72036-0911-05 Harris 5 patches — — FDA listed —
Amazon Basics Pain Relief Patch with 4% Lidocaine 4 g/100g 72288-0967-15 Amazon.com 15 patches — — FDA listed —
Signature Care Medicated Pain Relief Patch 4 g/100g 21130-0988-01 Safeway, 1 patch — — FDA listed —
Pain Relief Patches 4 g/100g 49035-0136-06 WALMART 6 patches — — FDA listed —
Thera Care Pain Therapy 4 g/100g 71101-0911-01 Veridian 1 patch — — FDA listed —
Meijer Lidocaine Pain Relief Patch Assortment Large 4 g/100g 79481-0003-02 Meijer 1 patch — — FDA listed —
Meijer Lidocaine Pain Relief Patch Assortment Small 4 g/100g 79481-0005-02 Meijer 1 patch — — FDA listed —
Dollar General Pain Relieving Patch with Lidocaine 4 g/100g 55910-0912-01 DOLGENCORP, 1 patch — — FDA listed —
Pain Relief Patches 4 g/100g 63940-0911-05 Liberty 5 patches — — FDA listed —
TheraCare Lidocaine Pain Relief 4 g/100g 71101-0125-01 Veridian 3 patches — — FDA listed —
Topcare Pain Relief Patches 4 g/100g 36800-0156-05 TOPCO 5 patches — — FDA listed —
Meijer Pain Relief Patches 4 g/100g 41250-0625-26 Meijer 6 patches — — FDA listed —
AsperFlex 4 g/100g 71399-4456-05 Akron 5 patches — — FDA listed —
Lidocaine 4% Patch 4 g/100g 87236-0023-01 Aldermed 1 g — — FDA listed —
Lidocaine 4% Patch 4 g/100gthis 87236-0024-05 Aldermed 5 pouches — — 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
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔓
·
Generic versions listed
see equivalents
✅Generic appears available

FDA-approved generic versions are listed, and recent pricing/market data suggests they may be available — see Therapeutic equivalents.

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 Lidocaine 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 X8AWZ2ZY3C
    A synthetic polymer made from acrylate compounds that forms a protective film or coating. It's used to coat tablets or capsules to control how quickly the medicine dissolves, protect the drug from stomach acid, or improve appearance.
  • UNII LKG8494WBH
    Benzyl alcohol is a clear liquid used as a preservative and solvent in medicines. It helps prevent bacterial and fungal growth and dissolves other ingredients to create uniform liquid formulations.
  • UNII REK4960K2U
    Butylated hydroxyanisole is a synthetic preservative that prevents oils and fats in medicines from spoiling or becoming rancid. It keeps the medicine stable and extends its shelf life.
  • 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 DO250MG0W6
    A mineral compound containing aluminum that acts as an antacid and buffering agent. It helps neutralize stomach acid and is used as a pH buffer to stabilize the medicine's formulation.
  • 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 2UMI9U37CP
    Oleic acid is a naturally occurring fatty acid derived from plant or animal oils. It functions as an emulsifier and solvent in medicines, helping blend water and oil-based ingredients together and dissolving other components.
  • 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 73861X4K5F
    A synthetic polymer used as a binder and thickening agent in tablets and capsules. It helps hold ingredients together and can modify how quickly the medicine dissolves and is absorbed in your body.
  • UNII 6OZP39ZG8H
    Polysorbate 80 is a synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together in medications and improves how the product disperses in the body.
  • UNII 532B59J990
    Polyvinyl alcohol is a synthetic polymer made from plant-derived materials. It's used as a binder to hold ingredients together, a film-former in coatings, and a thickener in liquid formulations.
  • 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 285CYO341L
    Sodium polyacrylate is a synthetic polymer that absorbs and holds water. In medicines, it acts as a disintegrant, helping tablets break apart quickly in the stomach, and as a binder, holding tablet ingredients together.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
  • 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 15FIX9V2JP
    Titanium dioxide is a bright white mineral powder commonly used as a colorant and opacifying agent. It makes pills and tablets white or lighter in color and helps make coatings non-transparent.
  • 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.

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

The official label also statesbenzyl alcohol, butylated hydroxyanisole, carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, edetate disodium, ethylhexylglycerin, glycerin, kaolin, methacrylate copolymer, oleic acid, phenoxyethanol, polyacrylic acid, polysorbate 80, polyvinyl alcohol, povidone, propylene glycol, sodium polyacrylate, sorbitol, tartaric acid, titanium dioxide, 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

LabelerAldermed Inc.
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code87236
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio23 products on file

More NDCs from Aldermed Inc. labeler code 87236

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 🤰 If Pregnant or Breast-Feeding 📄 Keep Out of Reach of Children 📄 Other Information 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 5 words ▾

Uses temporarily relieves minor pain.

⏱️ Dosage and Administration 69 words ▾

Directions adults and children over 12 years: clean and dry affected area, free of lotions, ointments and creams. Carefully remove backing from patch (see illustration). Apply sticky side of patch to affected area. apply 1 patch at a time to affected area, not more than 3 to 4 times daily remove patch from the skin after at most 8-hour application children under 12 years of age: consult a physician.

⚠️ Warnings 5 words ▾

Warnings For external use only

🧪 Active Ingredient 4 words ▾

Active ingredient Lidocaine 4%

🧪 Inactive Ingredients 37 words ▾

Inactive ingredients benzyl alcohol, butylated hydroxyanisole, carboxymethylcellulose sodium, dihydroxyaluminum aminoacetate, edetate disodium, ethylhexylglycerin, glycerin, kaolin, methacrylate copolymer, oleic acid, phenoxyethanol, polyacrylic acid, polysorbate 80, polyvinyl alcohol, povidone, propylene glycol, sodium polyacrylate, sorbitol, tartaric acid, titanium dioxide, water

🎯 Purpose 3 words ▾

Purpose Topical analgesic

📄 Do Not Use 29 words ▾

Do not use more than 1 patch at a time on wounds or damaged skin with a heating pad if you are allergic to any ingredients of this product

📄 When Using This Product 21 words ▾

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

📄 Stop Use and Ask a Doctor If 41 words ▾

Stop use and ask a doctor if skin reactions such as redness, itching, rash, excessive irritation, burning sensation, swelling or blistering occur conditions worsen symptoms persist for more than 7 days symptoms clear up and occur again within a few days

🤰 If Pregnant or Breast-Feeding 10 words ▾

If pregnant or breast-feeding, ask a health professional before use.

📄 Keep Out of Reach of Children 20 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. (1-800-222-1222)

📄 Other Information 16 words ▾

Other information store in a clean, dry place outside of direct sunlight. protect from excessive moisture.

📄 Questions or Comments 8 words ▾

Questions? Call 1-833-605-8474 9am - 5pm EST M-F

📄 Package Label / Principal Display Panel 59 words ▾

PRINCIPAL DISPLAY PANEL NDC 87236-024-01 Maximum Strength LIDOCAINE Pain Relief Patch LIDOCAINE 4% / TOPICAL ANALGESIC 1 Patch

3.93 IN x

5.51IN (10 cm x 14 cm) NDC 87236-024-05 Maximum Strength LIDOCAINE Pain Relief Patch LIDOCAINE 4% / TOPICAL ANALGESIC 5 Patches

3.93 IN x

5.51 IN (10 cm x 14 cm) Lidocaine 4% Pain Relief Patch label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

Medicare Part D spend CMS · PART D · 2026 (Q1)

Medicare Part D (outpatient prescription) spending for Lidocaine (matched by generic name) — the program that covers self-administered drugs. 17 manufacturers.
⚠️ Drug-level data: CMS publishes Part D spending by drug, not by NDC — these figures combine every manufacturer, strength and package size sold under the name Lidocaine. CMS lists 8 products for this generic; we show the highest-spend one. That’s a different level of aggregation than the Medicaid card above, which is specific to this exact 11-digit NDC (pack size included), so the two aren’t directly comparable.
Period
Total Part D spend
$53.12M
Claims incl. refills
593.7K
Beneficiaries
367.9K
Spend / beneficiary
$144.39
Spend / claim
$89.46
Trend by period
💵 About the dollar figures: spending is what Part D plans paid before confidential manufacturer rebates, so the program’s real net cost is lower. A blank patient count means fewer than 11 people — CMS hides counts that small to protect privacy. Source: CMS Medicare Quarterly Part D Spending by Drug (data.cms.gov), updated quarterly.

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Lidocaine 4% Patch (this brand).

Top reported reactions

Pain3,193
Nausea3,065
Fatigue3,054
Headache2,826
Dyspnoea2,175
Pneumonia2,006
Diarrhoea1,975

Reporter sex

49,106 reports
Male · 37%
Female · 63%
Unknown · 0%

Serious outcomes

Hospitalization17,671
Death4,997
Disabling1,211
Reports over time (by year) — tap or hover for the count & year
2021 2022 2024 2026 4,118 2,260
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 Aldermed Inc.. 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 1 g (87236-0024-01). 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?
Aldermed Inc. 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.
← 87236-0023-01 · Aldermed 87237-0001-01 · Gimmie →
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.