First Aid Burn Lidocaine Hydrochloride,Benzalkonium Chloride 5 mg/g; 1.3 mg/g Cream, 144 packets — NDC 82749-0009-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

First Aid Burn Lidocaine Hydrochloride,Benzalkonium Chloride 5 mg/g; 1.3 mg/g Cream, 144 packets — NDC 82749-009-01 (Billing 82749-0009-01)

by Epic Medical Supply Corp · 144 PACKET in 1 BOX / .9 g in 1 PACKET

This is a package of 144 packets of First Aid Burn Lidocaine Hydrochloride,Benzalkonium Chloride 5 mg/g; 1.3 mg/g Cream from Epic Medical Supply Corp, marketed since Jun 2024 and currently FDA-listed. It is this product's only package size.

NDC 82749-0009-01
🏷️ FDA NDC (as labeled) 82749-009-01 billing pads the product segment with a zero
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Aug 27, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

NDC database record

One package, one record: these facts belong to NDC 82749-009-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
82749 labeler · 009 product · 01 package
Package marketed since
Jun 1, 2024
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 8274900901 9
FDA record last changed
Aug 27, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 82749-009-01
Product NDC 82749-009
11-digit billing NDC 82749000901
RxCUI 1012100
UNII V13007Z41A, F5UM2KM3W7
Application # M017
SPL Set ID bd1b1873-e900-45eb-96a0-28f782b5a7cd
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 2024-06-01
Route TOPICAL
Dosage form CREAM
Substance LIDOCAINE HYDROCHLORIDE; BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1012100
Why two NDCs? The FDA registers this code as 82749-009-01 — 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 → 82749-0009-01. 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 Quaternary ammonium compounds class.

Drug family (ATC) Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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?

This is an over-the-counter topical cream marketed under FDA's OTC monograph rules for minor burn care. It contains lidocaine hydrochloride, a local anesthetic typically used to numb pain and discomfort at the skin surface, and benzalkonium chloride, an antimicrobial agent commonly used to help reduce bacteria on minor wounds. The cream is applied directly to the affected skin area.

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 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
82749-0009-01 You're viewing this Main listing 144 PACKET in 1 BOX / .9 g in 1 PACKET 2024-06-01 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
First Aid Only First Aid/Burn 5 mg/g; 1.3 mg/g 00924-5011-00 Acme 9 g — — FDA listed —
First Aid Only First Aid-Burn 1.3 mg/g; 5 mg/g 00924-5702-00 Acme 9 g — — FDA listed —
First Aid Only First Aid/Burn 5 mg/g; 1.3 mg/g 00924-5730-00 Acme 9 g — — FDA listed —
Xpect First Aid Cream .13 g/100g; .5 g/100g 42961-0259-02 Cintas 9 g — — FDA listed —
GENUINE FIRST AID Antiseptic Pain Relieving .13 g/100g; .5 g/100g 43473-0015-01 Nantong 9 g — — FDA listed —
SAFLY Burn .5 g/100g; .13 g/100g 43473-0039-01 Nantong 9 g — — FDA listed —
Firstar Burn .5 g/100g; .13 g/100g 43473-0040-01 Nantong 9 g — — FDA listed —
Aosi Healthcare Burn .5 g/100g; .13 g/100g 43473-0055-01 Nantong 9 g — — FDA listed —
health and beyond BURN .5 g/100g; .13 g/100g 43473-0064-01 Nantong 9 g — — FDA listed —
Proheal Burn .5 g/100g; .13 g/100g 43473-0066-01 Nantong 9 g — — FDA listed —
Everlit Care Burn .5 g/100g; .13 g/100g 43473-0113-01 Nantong 9 g — — FDA listed —
Burn with Lidocaine 1.3 mg/g; 5 mg/g 47682-0260-12 Unifirst 10 packets — — FDA listed —
Medi-First Burn with Lidocaine 1.3 mg/g; 5 mg/g 47682-0270-12 Unifirst 10 packets — — FDA listed —
Green Guard Derma-Caine Burn 1.3 mg/g; 5 mg/g 47682-0319-35 Unifirst 144 packets — — FDA listed —
Medi-First Plus Burn with Lidocaine 1.3 mg/g; 5 mg/g 47682-0930-73 Unifirst 25 packets — — FDA listed —
Medi-First Plus Burn Cream 5 mg/g; 1.3 mg/g 47682-0940-73 Unifirst 25 packets — — FDA listed —
Medi-First Burn with Lidocaine 1.3 mg/g; 5 mg/g 47682-0984-73 Unifirst 25 packets — — FDA listed —
Medi-First Plus Burn with Lidocaine 1.3 mg/g; 5 mg/g 47682-0985-73 Unifirst 25 packets — — FDA listed —
Burn Treatment .13 g/100g; .5 g/100g 49687-0014-00 CMC 10 pouches — — FDA listed —
Refill 3 .13 g/100g; .5 g/100g 49687-0017-00 CMC 9 g — — FDA listed —
First Aid and Burn .13 g/100g; .5 g/100g 50332-0037-01 HART 6 packets — — FDA listed —
First Aid and Burn .13 g/100g; .5 g/100g 50332-0091-01 HART 6 packets — — FDA listed —
Refill 3 .13 g/100g; .5 g/100g 50814-0017-01 GFA 9 g — — FDA listed —
Genuine First Aid First Aid Antiseptic Pain Relieving Cream 1.3 mg/g; 5 mg/g 50814-0059-01 GFA 9 g — — FDA listed —
Genuine First Aid Pain Relieving Cream 1.3 mg/g; 5 mg/g 50814-0079-01 GFA 9 g — — FDA listed —
CareALL First Aid Burn Cream .005 g/g; .0013 g/g 51824-0096-14 New 144 packets — — FDA listed —
Be Smart Get Prepared Burn Cream .13 g/100g; .5 g/100g 55550-0521-01 Total 9 g — — FDA listed —
Burn Cream 1.3 mg/g; 5 mg/g 55550-0902-21 Total 9 g — — FDA listed —
First Aid Burn Cream .5 g/100g; .13 g/100g 58228-2044-02 ProStat 25 packets — — FDA listed —
First Aid Burn Cream 50 mg/10000mg; 13 mg/10000mg 58228-2309-01 ProStat 2000 packets — — FDA listed —
2677 First Aid Burn Cream 13 mg/10000mg; 50 mg/10000mg 58228-2677-01 ProStat 10 packets — — FDA listed —
Burn Cream .0013 g/g; .005 g/g 58228-7000-01 Prostat 25 packets — — FDA listed —
Burn Cream .0013 g/g; .005 g/g 58228-7010-01 Prostat 10 packets — — FDA listed —
First Aid Burn .5 g/100g; .13 g/100g 59898-0902-01 Water-Jel 1728 packets — — FDA listed —
First Aid and Burn 1.3 mg/g; 5 mg/g 61010-5701-04 Safetec 144 packets — — FDA listed —
Burn First Aid 50 mg/10000mg; 13 mg/10000mg 67777-0007-50 Dynarex 144 packets — — FDA listed —
Burn Cream .005 g/g; .0013 g/g 69396-0105-09 Trifecta 144 packets — — FDA listed —
Burn Cream .005 g/g; .0013 g/g 69396-0124-09 Trifecta 25 packets — — FDA listed —
Burn Cream .005 g/g; .0013 g/g 69396-0136-10 Trifecta 10 packets — — FDA listed —
Burn Cream .005 g/g; .0013 g/g 69396-0146-10 Trifecta 10 packets — — FDA listed —
ECOLAB Burn Cream 5 mg/g; 1.3 mg/g 71338-0123-73 ECOLAB 25 packets — — FDA listed —
Medi-First 5 mg/g; 1.3 mg/g 71927-0019-02 Orazen 25 pouches — — FDA listed —
Ever Ready First Aid 5 mg/g; 1.3 mg/g 72976-0005-01 Ever 9 g — — FDA listed —
First Shield 5 mg/g; 1.3 mg/g 72976-0008-01 Ever 9 g — — FDA listed —
Burn .5 g/100g; .13 g/100g 73288-0007-01 NINGBO 9 g — — FDA listed —
Thompson Burn Cream with Lidocain 1.3 mg/g; 5 mg/g 73408-0060-12 Thompson 10 packets — — FDA listed —
Thompson Burn Cream with Lidocaine 5 mg/g; 1.3 mg/g 73408-0160-12 Thompson 10 packets — — FDA listed —
Crane Safety Burn 5 mg/g; 1.3 mg/g 73408-0260-12 Crane 10 packets — — FDA listed —
Thompson Burn Cream with Lidocaine 1.3 mg/g; 5 mg/g 73408-0940-73 Thompson 25 packets — — FDA listed —
Thompson Burn Cream with Lidocaine 5 mg/g; 1.3 mg/g 73408-0985-73 Thompson 25 packets — — FDA listed —
First Aid Burn 5 mg/g; 1.3 mg/gthis 82749-0009-01 Epic 144 packets — — FDA listed —
First Aid Antiseptic Pain Relieving 1.3 mg/g; 5 mg/g 82996-0002-01 Hubei 9 g — — FDA listed —
First Aid Antiseptic Pain Relieving Cream 1.3 mg/g; 5 mg/g 83165-0004-00 Hubei 1 patch — — FDA listed —
First Aid Antiseptic Pain Relieving Benzalkonium Chloride Lidocaine Hydrochloride 1.3 mg/g; 5 mg/g 84219-0002-00 M-star 9 g — — FDA listed —
First Aid Burn 5 mg/g; 1.3 mg/g 87251-0009-01 4 144 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

🏛️
2024
On the market since
Jun 2024
📍
2026
Currently FDA-listed
2 years 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerEpic Medical Supply Corp
FDA applicationM017 (OTC MONOGRAPH DRUG)
Labeler code82749
First marketedJun 2024
Product typeHuman Otc Drug
Portfolio3 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.

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 20 words ▾

Uses For temporary relief of pain and itching associated with: Sunburn Minor burns, Insect bites, Minor skin irritation, Cuts Scrapes

⏱️ Dosage and Administration 43 words ▾

Directions Adults and children 2 years and over : clean the affected area apply a small amount of this product on the area 3 to 4 times daily may be covered with a sterile bandage Children under 2 years : consult a doctor

⚠️ Warnings 98 words ▾

Warnings For external use only Do not use in the eyes over large areas of the body or on deep puncture wounds, animal bites, or serious burns in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if the condition gets worse condition clears up and recurs within a few days condition persists for more than 7 days If pregnant or breast feeding , ask a health care professional before use. Keep out of reach of children . If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

🧪 Active Ingredient 12 words ▾

Active Ingredients Lidocaine HCL 0.5% Topical Analgesic Benzalkonium Chloride 0.13% Topical Antiseptic

🧪 Inactive Ingredients 25 words ▾

Inactive ingredients Butylated Hydroxytoluene, Cetostearyl Alcohol, Dimethicone, Edetate Disodium, Glycerin, Glyceryl Monostearate, Isopropyl Myristate, Macrogol Cetostearyl Ether 20, Methylcellulose, Purified Water, Sodium Methylparaben, Sodium Propylparaben.

🎯 Purpose 5 words ▾

Purpose Topical Analgesic Topical Antiseptic

📄 Package Label / Principal Display Panel 4 words ▾

Product label image description

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

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 HYDROCHLORIDE,BENZALKONIUM CHLORIDE — the ingredient across all brands.

Top reported reactions

Anaphylactic Shock1
Bronchospasm1
Chills1
Dizziness1
Dysphagia1
Dyspnoea1
Erythema1

Reporter sex

1 reports
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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Epic Medical Supply Corp. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Epic Medical Supply Corp 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.
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.