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New Skin Bandage Benzethonium Chloride 1.8 mg/mL Liquid — NDC 16864-0440-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

New Skin Bandage Benzethonium Chloride 1.8 mg/mL Liquid — NDC 16864-440-01 (Billing 16864-0440-01) · Product 16864-440

by Advantice Health, LLC · 1 BOTTLE, WITH APPLICATOR in 1 BOX (16864-440-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR

NDC 16864-440-01 (billing 16864-0440-01) is a package of New Skin Bandage Benzethonium Chloride 1.8 mg/mL Liquid from Advantice Health, LLC, marketed since Mar 2011 and currently FDA-listed. It is the main listing for product NDC 16864-440, which comes in 5 package sizes.

NDC 16864-0440-01
🏷️ FDA NDC (as labeled) 16864-440-01 billing pads the product segment with a zero
This package
Contains30 mL in 1 bottle, with applicator Pack sizes5 compare ↓
Main listing for product 16864-440 · Also comes in: 10 mL 16864-440-02 13 mL 16864-440-03 8 packets 16864-440-04 16 packets 16864-440-05
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) 16864-440-01
Product NDC 16864-440
11-digit billing NDC 16864044001
NCPDP billing unit ML — per mL (volume)
UNII PH41D05744
UPC 0851409007011
Application # M003
SPL Set ID 60996119-8367-4e22-b6ec-c36490635fa4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2011-03-01
Route TOPICAL
Dosage form LIQUID
Substance BENZETHONIUM CHLORIDE

Drug-database identifiers Medi-Span GPI and First Databank GCN / HICL / AHFS classification

GCN Seq No 071092
GCN 34781
HICL code 004259
Ingredient (HICL) Benzethonium Chloride
HIC1 code Q
Therapeutic class — broad (HIC1) Ear/Eye/Nose/Rectum/Topical/Vagina/Other
HIC2 code Q5
Therapeutic class — intermediate (HIC2) Agents Acting Principally On The Skin
HIC3 code Q5B
Therapeutic class — specific (HIC3) Topical Preparations,Antibacterials
AHFS code 84:04.92.00
AHFS class Local Anti-Infectives, Miscellaneous
FDB label name NEW SKIN LIQUID BANDAGE
FDB brand name New Skin
Legend status O — Over-the-counter (OTC) drug or device
Quick answers for NDC 16864-440-01
  • GSN (GCN sequence number): 071092
  • GCN: 34781
  • HICL (First Databank): 004259
  • AHFS class code: 84:04.92.00
  • 11-digit billing NDC: 16864044001
Why two NDCs? The FDA registers this code as 16864-440-01 — 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 → 16864-0440-01. 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.

Clinical

Label name NEW SKIN LIQUID BANDAGE Ingredient Benzethonium Chloride
🧪 What is this product?

This is a topical liquid bandage containing benzethonium chloride, an antimicrobial agent. It is marketed as an over-the-counter monograph product, meaning it follows FDA's established rules for this category of topical antiseptic. Benzethonium chloride is typically used in liquid bandage products to help reduce bacteria on minor cuts, scrapes, and wounds. The liquid formulation allows application directly to the skin as a protective, antimicrobial coating.

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 mL 13 mL 8 packets 16 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
16864-0440-01 16864-440-01 You're viewing this Main listing 1 BOTTLE, WITH APPLICATOR in 1 BOX (16864-440-01) / 30 mL in 1 BOTTLE, WITH APPLICATOR 2011-03-01 — Active
16864-0440-02 16864-440-02 1 BOTTLE, WITH APPLICATOR in 1 BOX (16864-440-02) / 10 mL in 1 BOTTLE, WITH APPLICATOR 2011-03-01 — Active
16864-0440-03 16864-440-03 1 BOTTLE, WITH APPLICATOR in 1 BOX (16864-440-03) / 13 mL in 1 BOTTLE, WITH APPLICATOR 2011-03-01 — Active
16864-0440-04 16864-440-04 8 PACKET in 1 BOX (16864-440-04) / 8 mL in 1 PACKET 2026-01-01 — Active
16864-0440-05 16864-440-05 16 PACKET in 1 BOX (16864-440-05) / 8 mL in 1 PACKET 2026-01-01 — Active

Pack size FAQ

What quantity is in NDC 16864-0440-01?
NDC 16864-0440-01 is listed by the FDA — 1 bottle, with applicator in 1 box / 30 ml in 1 bottle, with applicator.
What NDC number is used to bill for this package of New Skin Bandage Benzethonium Chloride 1.8 mg/mL Liquid?
Bill NDC 16864-0440-01 — the 11-digit billing format is 16864044001. 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
New Skin Bandage 1.8 mg/mLthis 16864-0440-01 Advantice 1 bottle — — 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
Mar 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.

What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 1364PS73AF
    Acetone is a clear, volatile liquid solvent. In medications, it helps dissolve or extract active ingredients during manufacturing and may be used in certain liquid formulations or coating processes.
  • 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 92Q24NH7AS
    Amyl acetate is a clear liquid solvent derived from amyl alcohol and acetic acid. In medicines, it's used as a solvent in liquid formulations and as a processing agent to help dissolve or suspend active ingredients.
  • UNII 464P5N1905
    Butyl acetate is a clear liquid solvent derived from acetic acid and butanol. In medications, it's used primarily in coatings and varnishes to help dissolve and apply protective or delayed-release layers on tablets and capsules.
  • UNII N20HL7Q941
    Camphor is a waxy, aromatic substance derived from camphor tree wood or made synthetically. In medicines, it typically serves as a preservative, flavoring agent, or mild skin irritant in topical products.
  • UNII 76845O8NMZ
    Ethyl acetate is a clear, colorless liquid solvent derived from acetic acid and ethanol. In medicines, it dissolves active ingredients, carries them into the product formulation, and helps control how quickly the drug releases and works in your body.
  • UNII KYR8BR2X6O
    Pyroxylin is a cellulose derivative made by treating plant fibers with nitric acid. It serves as a film-former and binder in medications, helping create coatings on tablets and capsules or holding ingredients together in solid dosage forms.

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

The official label also statesamyl acetate, butyl acetate, camphor, ethyl acetate, nitrocellulose, SD alcohol 3-C (7.2% v/v)

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

LabelerAdvantice Health, LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code16864
First marketedMar 2011
Product typeHuman Otc Drug
Portfolio11 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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Ask a Doctor Before Use If 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Use first aid to help prevent bacterial contamination in minor cuts and scrapes

⏱️ Dosage and Administration 36 words ▾

Directions clean affected area apply small amount on the area 1–3 times daily let dry a second coating may be applied for extra protection to remove, apply more New-Skin ® Liquid Bandage and quickly wipe off

⚠️ Warnings 137 words ▾

Warnings For external use only Flammable keep away from fire or flame Do not use in the eyes over large areas of the body longer than one week unless directed by a doctor on infected areas or wounds that are draining with other first aid products such as lotions and creams over sutures on mucous membranes Ask a doctor before use if you have deep or puncture wounds deep cuts animal bites serious bleeding diabetes poor circulation serious burns When using this product do not store at temperatures above 120°F intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal Stop use and ask a doctor if condition persists or gets worse infection occurs Keep out of reach of children.

If swallowed, get medical help or call a Poison Control Center right away.

📦 Storage and Handling 37 words ▾

Other information store at 20-25°C (68-77°F), away from heat may temporarily sting upon application keep carton for full drug facts do not allow to come into contact with floors, countertops or other finished surfaces – will stain

🧪 Active Ingredient 5 words ▾

Active ingredient Benzethonium chloride 0.2%

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients amyl acetate, butyl acetate, camphor, ethyl acetate, nitrocellulose, SD alcohol 3-C (7.2% v/v)

🎯 Purpose 4 words ▾

Purpose First aid antiseptic

📄 Do Not Use 44 words ▾

Do not use in the eyes over large areas of the body longer than one week unless directed by a doctor on infected areas or wounds that are draining with other first aid products such as lotions and creams over sutures on mucous membranes

📄 Ask a Doctor Before Use If 23 words ▾

Ask a doctor before use if you have deep or puncture wounds deep cuts animal bites serious bleeding diabetes poor circulation serious burns

📄 When Using This Product 25 words ▾

When using this product do not store at temperatures above 120°F intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal

📄 Stop Use and Ask a Doctor If 14 words ▾

Stop use and ask a doctor if condition persists or gets worse infection occurs

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Questions or Comments 2 words ▾

Questions? 1-800-345-0032

📄 Package Label / Principal Display Panel 52 words ▾

PRINCIPAL DISPLAY PANEL - 30 mL Bottle Box new- Skin ® Benzethonium Chloride 0.2%/First Aid Antiseptic LIQUID BANDAGE Brush ALL-IN-ONE PROTECTION Prevents Infection Seals Out Water, Dirt & Germs Helps Heal Cuts #1 pharmacist recommended Works Where Bandages Can't

1.0 FL OZ (30 mL) PRINCIPAL DISPLAY PANEL - 30 mL Bottle Box

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 FDA registers it as 16864-440-01, 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: 16864-0440-01, written without dashes as 16864044001. 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 16864-0440-01, the first segment (16864) is the labeler code FDA assigned to Advantice Health, LLC; the middle segment (0440) 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 Advantice Health, LLC. 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 4 other package presentations of this same product, including 1 bottle (16864-0440-02), 1 bottle (16864-0440-03), 8 packets (16864-0440-04). Each has its own NDC and its own page — see the package list near the top of this page.
Who lists this product with the FDA?
Advantice Health, LLC 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.
← 16864-0240-01 · Advantice 16864-0450-01 · Advantice →
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.