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Antiseptic alcohol, lidocaine hydrochloride 500 mg/g; 20 mg/g Liquid, 25 packets — NDC 61010-5200-07 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Antiseptic alcohol, lidocaine hydrochloride 500 mg/g; 20 mg/g Liquid, 25 packets — NDC 61010-5200-7 (Billing 61010-5200-07)

by Safetec of America, Inc. · 25 PACKET in 1 BOX / 1.8 g in 1 PACKET

This is a package of 25 packets of Antiseptic alcohol, lidocaine hydrochloride 500 mg/g; 20 mg/g Liquid from Safetec of America, Inc., marketed since Sep 2011 and currently FDA-listed.

NDC 61010-5200-07
🏷️ FDA NDC (as labeled) 61010-5200-7 billing pads the package segment with a zero
This package
Contains25 packets Pack sizes6 compare ↓
Product page 61010-5200-01 Also comes in: 10 packets 61010-5200-5 20 packets 61010-5200-6 56 g 61010-5200-1 100 packets 61010-5200-2 150 packets 61010-5200-4
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 2026 · this listing last changed Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61010-5200-7
Product NDC 61010-5200
11-digit billing NDC 61010520007
UNII 3K9958V90M, V13007Z41A
Application # M003
SPL Set ID 71aeaf86-2b4d-4945-9606-a9db0ab6b726
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 2011-09-30
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL; LIDOCAINE HYDROCHLORIDE
Why two NDCs? The FDA registers this code as 61010-5200-7 — a 5-4-1 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 package segment → 61010-5200-07. 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.

Clinical

🧪 What is this product?

This is a topical liquid antiseptic and local anesthetic product sold over the counter under FDA's OTC monograph rules. It contains alcohol, which is commonly used as an antiseptic to help reduce bacteria on skin, and lidocaine hydrochloride, a local anesthetic that is typically used to numb minor skin irritation or discomfort. The combination is intended for application to intact skin surfaces.

Supplement & herbal interactions

🌿 Drug–supplement interaction checker →
Where does this data come from?
Plain-language summary from MedlinePlus (U.S. National Library of Medicine); supplement & herbal interactions and nutrient depletion data from the Natural Medicines database; our full guide is HelloPharmacist editorial content.

Pricing

A drug doesn't have one price. Each row is a different public payment system, and none is what you'd pay at the counter — that depends on your insurance. The ⓘ on each row explains what it measures.

Price systemPer mLPer package
Retail pharmacies payNADAC · weekly Not in the retail survey — common for institutional, discontinued, or low-volume packs.
Medicaid paysCMS SDUD · 12 mo No recent Medicaid claims on file for this NDC — rare and low-volume NDCs are suppressed in the public data.
Medicare drug plans payPart D · quarterly No Part D plan price is available for this NDC in our data.
ℹ️
No price is published for this exact package yet. CMS surveys NADAC per package size, so a different pack of the same drug often has one.
Try another pack size: 10 packets 20 packets 56 g 100 packets 150 packets
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
61010-5200-01 61010-5200-1 Main listing 56 g in 1 BOTTLE 2011-09-30 — Active
61010-5200-02 61010-5200-2 100 PACKET in 1 BOX / 1.8 g in 1 PACKET 2011-09-30 — Active
61010-5200-04 61010-5200-4 150 PACKET in 1 BOX / .8 g in 1 PACKET 2011-09-30 — Active
61010-5200-05 61010-5200-5 10 PACKET in 1 BOX / .8 g in 1 PACKET 2011-09-30 — Active
61010-5200-06 61010-5200-6 20 PACKET in 1 BOX / 1.8 g in 1 PACKET 2011-09-30 — Active
61010-5200-07 You're viewing this 25 PACKET in 1 BOX / 1.8 g in 1 PACKET 2011-09-30 — Active

Pack size FAQ

What quantity is in this package?
This package contains 25 packets — 25 packet in 1 box / 1.8 g in 1 packet.
How does this package differ from NDC 61010-5200-05?
Both are Antiseptic alcohol, lidocaine hydrochloride 500 mg/g; 20 mg/g Liquid — the drug itself is identical. This page's package is the 25 packets one, while NDC 61010-5200-05 is the 10 packets package.
What NDC number is used to bill for this package of Antiseptic alcohol, lidocaine hydrochloride 500 mg/g; 20 mg/g Liquid?
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
Antiseptic 500 mg/g; 20 mg/gthis 61010-5200-07 Safetec 25 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

🏛️
2011
On the market since
Sep 2011
📍
2026
Currently FDA-listed
15 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.

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

  • UNII F5UM2KM3W7
    Benzalkonium chloride is a chemical compound that works as a preservative and antimicrobial agent in medications. It prevents bacterial and fungal growth in liquid formulations to keep the product safe during storage and use.
  • UNII L7T10EIP3A
    A cooling compound from mint plants used as a flavoring agent and to create a fresh sensation in medicines. It helps mask bitter tastes and improve how the product feels in the mouth.
  • 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.

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

The official label also statesInactive ingredients benzalkonium chloride, menthol, purified 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

LabelerSafetec of America, Inc.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code61010
First marketedSep 2011
Product typeHuman Otc Drug
Portfolio33 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 ⏱️ Dosage and Administration ⚠️ Warnings 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 18 words ▾

Uses First aid to help prevent infection in minor scrapes and temporary relief of itching of insect bites

⏱️ Dosage and Administration 35 words ▾

Directions adults and children 2 years and older: Apply to cleaned affected area not more than 3 times daily. children under 2 years of age: Consult a doctor. Inactive ingredients benzalkonium chloride, menthol, purified water

⚠️ Warnings 72 words ▾

Warnings For external use only. Flammable, keep away from fire or flame. Do not use over large areas of the body in eyes over raw or blistered areas Stop use and ask doctor if conditions worsen or persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away

🧪 Active Ingredient 8 words ▾

Active Ingredients Ethyl alcohol 50.0% Lidocaine HCl 2.0%

🧪 Inactive Ingredients 7 words ▾

Inactive ingredients benzalkonium chloride, menthol, purified water

🎯 Purpose 6 words ▾

Purpose First Aid Antiseptic Topical Analgesic

📄 Do Not Use 16 words ▾

Do not use over large areas of the body in eyes over raw or blistered areas

📄 Stop Use and Ask a Doctor If 25 words ▾

Stop use and ask doctor if conditions worsen or persist for more than 7 days or clear up and occur again within a few days.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children If swallowed get medical help or contact a Poison Control Center right away

📄 Package Label / Principal Display Panel 145 words ▾

PRINCIPAL DISPLAY PANEL – mini pouch label Safetec Sting Relief Insect Bite Antiseptic and Pain Reliever Contents: 1 single-use, premoistened towelette Manufactured by SAFETEC OF AMERICA, Inc. Buffalo, NY 14215 800-456-7077 www.safetec.com EXP. LOT PRINCIPAL DISPLAY PANEL – mini pouch label

PRINCIPAL DISPLAY PANEL – 150 count box Safetec NDC 61010-5200-4 Sting Relief Insect Bite Antiseptic and Pain Reliever Reorder No. 52004 Contents: 150 single-use, premoistened towelettes PRINCIPAL DISPLAY PANEL – 150 count box

PRINCIPAL DISPLAY PANEL – 2 fl. oz. bottle NDC 61010-5200-1 Safetec Sting Relief Insect Bite Antiseptic and Pain Reliever 2 fl. oz. (59.1 ml) Reorder No. 52001 Package Not Child Resistant PRINCIPAL DISPLAY PANEL – 2 fl. oz. bottle

Principal Display Panel – 25 Count Box Label NDC 61010-5200-7 Safetec Sting Relief Insect Bite Antiseptic and Pain Reliever Contents: 25 single-use, premoistened towelettes Principal Display Panel – 25 Count Box Label

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 Safetec of America, 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 5 other package presentations of this same product, including 10 packets (61010-5200-05), 20 packets (61010-5200-06), 56 g (61010-5200-01). 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?
Safetec of America, 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.
← 61010-5111-00 · Safetec 61010-5300-00 · Safetec →
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.