HomeNDC LookupIngredientsLidocaine Hydrochloride › 71101-0102-01
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(from DailyMed)

HealthWise 4% Lidocaine Cream 2.7 oz LIDOCAINE HYDROCHLORIDE 4 g/100g Cream, 1 bottle

by Veridian Healthcare · 1 BOTTLE, PLASTIC in 1 CARTON (71101-102-01) / 76.5 g in 1 BOTTLE, PLASTIC
NDC 71101-0102-01
🏷️ FDA NDC (as labeled) 71101-102-01 billing pads the product segment with a zero
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 →
⚠️
Other active recalls for Lidocaine Hydrochloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Jul 16, 2026 — Presence of Particulate Matter: Hair was found in products (Fresenius Kabi USA, LLC) · FDA recall D-0726-2026
Class II · Jun 8, 2026 — Lack of Assurance of Sterility (Asclemed USA Inc.) · FDA recall D-0658-2026
Class II · Apr 2, 2026 — Lack of Assurance of Sterility (Huons Co., Ltd.) · FDA recall D-0529-2026
Class II · Apr 2, 2026 — Lack of Assurance of Sterility (Huons Co., Ltd.) · FDA recall D-0532-2026
Class II · Nov 30, 2021 — Superpotent Drug: Minimally superpotent (Teligent Pharma, Inc.) · FDA recall D-0296-2022
Class I · Nov 30, 2021 — Superpotent Drug (Teligent Pharma, Inc.) · FDA recall D-0295-2022
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 71101-102-01
Product NDC 71101-102
11-digit billing NDC 71101010201
RxCUI 1010895
UNII V13007Z41A
Application # M017
SPL Set ID f39eb3d0-e153-4f50-85b1-ad5c677d176c
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 2025-08-01
Route TOPICAL
Dosage form CREAM
Substance LIDOCAINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 71101-102-01 — 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 → 71101-0102-01. 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.

🏭 Manufacturer & labeler

LabelerVeridian Healthcare
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code71101
First marketedAug 2025
Product typeHuman Otc Drug
Portfolio130 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

📗 Our plain-language guide HelloPharmacist
  • It's best to avoid using two lidocaine products at the same time unless your doctor says it's okay. When you use multiple products containing a local anesthetic, the total amount a...
  • Can I use a lidocaine patch and a lidocaine cream at the same time?
  • No — please don't do this. Heat significantly increases how much lidocaine is absorbed through your skin, which can push drug levels in your blood higher than they should be. Stick...
  • Can I put a heating pad on the area where I applied 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.

🧪 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 3K9958V90M
    A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 2DMT128M1S
    A waxy solid derived from plant or animal sources. It acts as an emulsifier to blend oil and water components, and also thickens the medicine to give it the right texture and consistency.
  • UNII 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • 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 86FQE96TZ4
    A synthetic polymer, this ingredient acts as a thickener and suspending agent in liquid formulations. It helps maintain uniform consistency and keeps particles evenly distributed throughout the medicine.
  • UNII 603P14DHEB
    A synthetic antimicrobial chemical used as a preservative in topical and cosmetic formulations. It prevents bacterial and fungal growth in products to maintain stability and safety during storage and use.
  • 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 9G2MAD7J6W
    Polyacrylic acid is a synthetic polymer used as a binder and thickening agent in medicines. It helps hold tablet ingredients together and can increase the viscosity of liquid or semi-solid formulations.
  • UNII CAL22UVI4M
    A synthetic emulsifier derived from sorbitol and fatty acids. It helps mix oil and water-based ingredients together and improves the texture and stability of the medicine.
  • UNII WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII V56DFE46J5
    Steareth-2 is a synthetic emulsifier made from stearic acid and ethylene oxide. It helps mix oil and water-based ingredients together in the formulation and may improve how the medicine spreads or dissolves.
  • UNII 53J3F32P58
    A synthetic detergent derived from stearic acid, a fatty substance. It helps dissolve or distribute oil-based ingredients evenly throughout the medicine, acting as an emulsifier and solubilizer in tablets and capsules.
  • 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.

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

The official label also statesaloe vera extract,cetostearyl alcohol,dimethicone, edetate disodiumanhydrous,ethyl alcohol,ethylhexylglycerin, hydroxyethyl acrylate/sodium acryloyldimethyl tauratecopolymer, iodopropynyl butylcarbamate, monostearin, phenoxyethanol, polyacrylic acid, potassiumhydroxide, steareth-2, steareth-21, tween 60, 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 DailyMedingredient 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 gPer 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
GNP Lidocaine Maximum Strength 4 g/100g 46122-0614-10 AMERISOURCE 1 bottle $0.052 Availability likely
Leader 4 g/100g 70000-0098-01 Cardinal 1 bottle $0.052 Availability likely
Lidocaine HCL 4 g/100g 87137-0101-07 Matthias 1 bottle $0.052 Availability likely
Pain and Itch Relief 4% Lidocaine .04 g/40g 00363-3001-24 Walgreens 1 tube FDA listed
Walgreens Pain Relieving Cream 4 g/100g 00363-3037-02 Walgreens 76.5 g FDA listed
Mentholatum Lidocaine Heat 40 mg/mL 10742-8386-01 The 1 bottle FDA listed
Signature Care Lidocaine Cream 40 mg/g 21130-0544-27 Better 1 bottle FDA listed
Kroger Analgesic Analgesic 40 mg/g 30142-0260-01 THE 1 bottle FDA listed
TopCare Pain Relieving Analgesic 40 mg/g 36800-0470-01 Topco 1 bottle FDA listed
Gold Bond Medicated Pain and Itch Relief 4 g/100g 41167-0529-00 Chattem, 1 bottle FDA listed
Aspercreme Lidocaine with Rosemary and Mint 4 g/100g 41167-0565-00 Chattem, 1 bottle FDA listed
Aspercreme Lidocaine with Eucalyptus Essential Oil 4 g/100g 41167-0566-00 Chattem, 1 tube FDA listed
Aspercreme with Lidocaine Pain Relieving Creme 4 g/100g 41167-0582-01 Chattem, 1 bottle FDA listed
Aspercreme with Lidocaine Foot Pain Creme 4 g/100g 41167-0586-02 Chattem, 1 bottle FDA listed
Aspercreme with Lidocaine Pain Relieving Creme 4 g/100g 41167-0587-07 Chattem, 1 bottle FDA listed
Aspercreme Lidocaine Foot (Diabetic) 4 g/100g 41167-0597-00 Chattem, 1 bottle FDA listed
LidoStat 40 mg/g 44577-0704-02 Clinical 1 tube FDA listed
Equate Pain Relief Cream 4 mg/100mL 49035-0634-97 Walmart, 74 ml FDA listed
Equate Pain Relieving Cream Lidocaine 40 mg/g 49035-0860-01 Wal-Mart 1 bottle FDA listed
CVS Lidocaine Pain Relief Cream 40 mg/g 51316-0379-43 CVS 1 bottle FDA listed
Launch Medical 4 g/100mL 54723-0018-01 Sambria 30 ml FDA listed
BeardedMoney 4 g/100g 54723-0032-01 Sambria 15 g FDA listed
NeuroMed 7 Topical Pain Relief 4 g/100g 54723-0175-22 Sambria 1 tube FDA listed
DG Health Pain Relieving 40 mg/g 55910-0759-01 DOLGENCORP, 1 bottle FDA listed
T-Relief Lidocaine HCL 4% 3.4 g/85g 62795-6050-07 Medinatura 85 g FDA listed
QC Lidocaine Maximum Strength 4 g/100g 63868-0956-01 Chain 1 bottle FDA listed
Pain Itch Relief 4 g/100g 69396-0120-17 Trifecta 1 bottle FDA listed
Lidocaine 4 Percent 4 g/100g 69420-6262-01 SA3, 120 g FDA listed
CVS Health Lidocaine Cream 40 mg/g 69842-0814-77 CVS 1 bottle FDA listed
CVS Lidocaine Maximum Strength 4 g/100g 69842-0921-49 CVS 1 bottle FDA listed
CVS Health Lidocaine Pain Relief 40 mg/g 69842-0980-01 CVS 1 bottle FDA listed
BENGAY Tropical Jasmine 40 mg/g 69968-0614-03 Kenvue 1 tube FDA listed
NumbR-X 4 g/100g 70171-0001-01 Prodigy 1 jar FDA listed
Dr Lido 4 g/100g 70171-0002-01 Prodigy 1 jar FDA listed
Inked Inspired 4 g/100g 70171-0003-01 Prodigy 1 jar FDA listed
Dr Tatty Numbing 4 g/100g 70171-0020-01 Prodigy 1 jar FDA listed
TattooGirl Numbing 4 g/100g 70171-0021-01 Prodigy 1 tube FDA listed
InkKulture Numbing 4 g/100g 70171-0022-01 Prodigy 1 tube FDA listed
Inkorporated Numbing 4 g/100g 70171-0028-01 Prodigy 1 jar FDA listed
Ink Scribd Numbing 4 g/100g 70171-0029-01 Prodigy 1 jar FDA listed
LidoPlus Pain Relief 40 mg/mL 70372-0723-01 Centura 1 tube FDA listed
TheraCare Pain Relieving Lidocaine Cream 4 g/100g 71101-0056-01 Veridian 1 bottle FDA listed
TheraCare Pain Relieving Lidocaine Cream 4 g/100g 71101-0057-01 Veridian 1 bottle FDA listed
HealthWise 4% Lidocaine Cream 2.7 oz 4 g/100gthis 71101-0102-01 Veridian 1 bottle FDA listed
HealthWise Pain Relief Lidocaine 4 g/100g 71101-0107-47 Veridian 1 bottle FDA listed
HealthWise 4% Lidocaine Cream 4 g/100g 71101-0919-27 Veridian 1 bottle FDA listed
TheraCare 4% Lidocaine Cream 4 g/100g 71101-0930-01 Veridian 1 bottle FDA listed
HealthWise Pain Relief Cream with Lidocaine 4 g/100g 71101-0932-01 Veridian 1 bottle FDA listed
Lidocaine HCl 4 Percent 4 g/100g 71436-0026-01 ARI 120 g FDA listed
Lidozall Plus 4 g/100g 72835-0114-15 V2 15 packets FDA listed
Lidozall Pro 4 g/100g 72835-0445-05 V2 5 packets FDA listed
DCH Pain Relief 4 g/100g 72839-0361-02 Derma 76.5 g FDA listed
SUGAR BRANDS Rescue Pain Relief and Recovery 40 mg/mL 73313-0075-04 Sugar 118 ml FDA listed
Lidocaine HCI 40 mg/g 73352-0204-60 Trifluent 30 g FDA listed
LidoGuard 4 g/100g 73492-0272-30 ALAINA 1 tube FDA listed
TopCare Pain Relieving Cream 40 mg/g 76162-0291-02 Topco 1 bottle FDA listed
Sting Master 40 mg/g 80324-0078-00 Les 1 jar FDA listed
Lidocaine Pain Relief Roll-On 4 g/100mL 82645-0013-97 Pharma 1 bottle FDA listed
Westlake Lidocaine 4 g/100g 82895-0717-50 Westlake 1 bottle FDA listed
Westlake Outdoor Pain and Itch Relieving 40 mg/g 82895-0718-50 WESTLAKE 49 g FDA listed
Lidocore 3.1 g/76.5g 82944-0201-02 iON 1 bottle FDA listed
Gold Bond Maximum Strength Foot Pain Relief 4 g/100g 84714-0427-06 Gold 1 bottle FDA listed
Gold Bond Medicated Pain and Itch Relief 4 g/100g 84714-0529-00 Gold 1 bottle FDA listed
Ikonik Tonik 4 g/100mL 85132-0001-30 IKONIK 1 tube FDA listed
LidoGuard 4 g/100g 85231-0200-30 ViolaCare, 1 tube FDA listed
Alcemiste 4 g/100mL 87087-0001-01 Price 1 jar FDA listed
Tattoo Numbx Numbing Pain Relieving 40 mg/mL 87460-0905-00 Scyberco 1 tube FDA listed
Tattoo Numbing Cream Co 4 g/100g 54723-0023-01 Sambria 1 tube FDA listed
TattooNumb 4 g/100g 54723-0030-01 Sambria 10 g FDA listed
Lidozall 4 g/100g 72835-0004-20 V2 20 packets FDA listed
Arte Maximum strength Numbing Cream 4 g/100g 54723-0024-01 Sambria 30 g FDA listed
Walgreens Burn 4 g/100g 00363-2020-25 WALGREENS 1 tube FDA listed
ZyloRelief 4 g/100g 87450-0208-15 Highmark 5 packets 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
Aug 2025
📍
2026
Currently FDA-listed
1 year listed
🔓
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
71101-0102-01 You're viewing this 1 BOTTLE, PLASTIC in 1 CARTON (71101-102-01) / 76.5 g in 1 BOTTLE, PLASTIC 2025-08-01 Active

🧭 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 — 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.
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 71101-102-01, 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: 71101-0102-01, written without dashes as 71101010201. 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 71101-0102-01, the first segment (71101) is the labeler code FDA assigned to Veridian Healthcare; the middle segment (0102) 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 Veridian Healthcare. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Veridian Healthcare 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 5 words

Use temporarily relieves minor pain

⏱️ Dosage and Administration 37 words

Directions adults and children over 12 years: apply a thin layer to affected area every 6 to 8 hours, not to exceed 3 applications in a 24 hour period children 12 years or younger: ask a doctor

⚠️ Warnings 134 words

Warnings For external use only. Avoid contact with eyes. Do not use Do not use ■ in large quantities, particularly over raw surfaces or blistered areas ■on puncture wounds■for more than one week without consulting a doctor When using this product use only as directed.

Read and follow all directions and warnings on this carton. do not allow contact with the eyes do not bandage or apply local heat (such as heating pads) to the area of use Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (800-222-1222) right away.

🧪 Active Ingredient 5 words

Active ingredient Lidocaine HCl 4%

🧪 Inactive Ingredients 25 words

Inactive ingredients aloe vera extract,cetostearyl alcohol,dimethicone, edetate disodiumanhydrous,ethyl alcohol,ethylhexylglycerin, hydroxyethyl acrylate/sodium acryloyldimethyl tauratecopolymer, iodopropynyl butylcarbamate, monostearin, phenoxyethanol, polyacrylic acid, potassiumhydroxide, steareth-2, steareth-21, tween 60, water

🎯 Purpose 3 words

Purpose Topical analgesic

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