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ALTA ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE .13 g/100g Cloth, 1 packet — NDC 79165-0777-20 package photo

ALTA ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE .13 g/100g Cloth, 1 packet

by Alta Sales Inc · 20 PACKAGE in 1 PACKET (79165-777-20) / 3.6 g in 1 PACKAGE
NDC 79165-0777-20
🏷️ FDA NDC (as labeled) 79165-777-20 billing pads the product segment with a zero
This package
Contains1 packet Pack sizes2 compare ↓
Also comes in: 3.6 g 79165-0777-90
OTC On market Non-controlled
🗂️ Data synced Aug 6, 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

⚠️
Other active recalls for Benzalkonium Chloride (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 · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0374-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 79165-777-20
Product NDC 79165-777
11-digit billing NDC 79165077720
RxCUI 1038558
UNII F5UM2KM3W7
UPC 0379165777905
Application # 505G(a)(3)
SPL Set ID 9064a1b1-dd4a-4f74-99c4-5ea93b4be210
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-07-01
Route TOPICAL
Dosage form CLOTH
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 79165-777-20 — 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 → 79165-0777-20. 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.

🏭 Manufacturer & labeler

LabelerAlta Sales Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code79165
First marketedJul 2020
Product typeHuman Otc Drug
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

🧪 What is this product?

This is an over-the-counter antibacterial hand wipe cloth containing benzalkonium chloride, a topical antimicrobial agent. The cloth is designed for cleaning and disinfecting hands and skin surfaces. Benzalkonium chloride is commonly used in hand sanitizers and antiseptic products to reduce bacteria on the skin. These wipes are marketed as an OTC monograph product, meaning they follow established FDA guidelines for this category of antiseptic cleaners.

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 8SKN0B0MIM
    Benzoic acid is a naturally occurring organic acid used as a preservative in medicines and foods. It helps prevent bacterial and fungal growth to extend shelf life and maintain product stability.
  • UNII 2968PHW8QP
    A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
  • UNII 5OCF3O11KX
    A plant-derived surfactant made from coconut oil. It helps mix oil and water ingredients together in the formulation and can improve how the medicine spreads or feels on the skin.
  • UNII 2KAG279R6R
    Dehydroacetic acid is a synthetic preservative that prevents mold, yeast, and bacterial growth in medicines. It extends shelf life by protecting the product from spoilage during storage and use.
  • UNII MP1J8420LU
    A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend 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 VNX7251543
    A plant-derived emulsifier made from coconut oil and polyethylene glycol. It helps mix oil and water-based ingredients together and improves how the medicine spreads or absorbs.
  • 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 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • 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 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.

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

The official label also statesAqua, Phenoxyethanol, Perfume, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Benzoic acid, Tetrasodium Edta, Dehydroacetic acid, Glycerin, Polysorbate 20, Citric acid

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.

💲 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: 3.6 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Antibacterial Wet Wipes .13 g/100g 70412-0500-10 Zhejiang 10 patches — — FDA listed —
FIRSTAR BZK Antiseptic Towelette .13 g/100g 71734-0111-01 JIANGMEN 2 g — — FDA listed —
Antibacterial Wet Wipes .13 g/100g 73015-0001-01 HangZhou 15 pouches — — FDA listed —
Antibacterial Wipes .13 g/100g 81079-0001-01 SHAOXING 38 g — — FDA listed —
Biopure Anti-bacterial Hand Wipes Fresh Morning Breeze Scent .13 g/100g 78691-0032-00 Quest 20 g — — FDA listed —
Klean Freak .13 g/100g 78982-0002-01 KLEAN 4 g — — FDA listed —
Zoviro .13 g/100g 83814-0003-01 Zoviro, 80 pouches — — FDA listed —
Zehn Antiseptic Sanitizing Wipes .13 g/100g 84488-0002-01 Zehn 1500 patches — — FDA listed —
SimplyGreat Antibacterial wet wipes .13 g/100g 85057-0001-01 Simply 40 patches — — FDA listed —
Clorox Hand Sanitizer .13 g/100g 69540-0036-01 Brand 20 patches — — Discontinued —
Hand Wipes .13 g/100g 77677-0013-20 Advanced 20 packets — — FDA listed —
Zoviro .13 g/100g 83814-0001-01 Zoviro, 20 pouches — — FDA listed —
Sipa HAND SANITIZING WIPES .13 g/100g 85137-0001-01 Sipa 50 patches — — FDA listed —
Value Wipes .13 g/100g 72202-0013-80 Zogics, 800 packets — — FDA listed —
Sanitizing Wipes .13 g/100g 72202-0200-01 Zogics, 2000 packets — — FDA listed —
Terramed Just Think Comfort Armor Antibacterial Cleansing Bar .13 g/100g 83004-0033-01 Rida 120 g — — FDA listed —
Zehn Antiseptic Sanitizing Wipes .13 g/100g 84488-0001-01 Zehn 10 patches — — FDA listed —
MedPride Bath Wipes .13 g/100g 52410-4107-07 Shield 13 g — — FDA listed —
Sanitex Antibacterial Hand Wipes Fresh Scent .13 g/100g 53118-0002-01 Precare 1 canister — — FDA listed —
MediChoice Cleansing .13 g/100g 39892-0305-01 O&M 1000 patches — — FDA listed —
Klean Freak .13 g/100g 78982-0004-01 KLEAN 4 g — — FDA listed —
Biopure20Ct Anti Bacterial Hand Wipes .13 g/100g 79794-0114-01 Zhejiang 480 patches — — FDA listed —
MediChoice BZK Antiseptic .13 g/100g 39892-0304-01 O&M 1000 patches — — FDA listed —
Antibacterial Wipes .13 g/100g 52000-0419-80 Universal 337 g — — Discontinued —
Antibacterial Wipes .13 g/100g 71293-0020-01 ERC 2000 packets — — FDA listed —
Klean Freak .13 g/100g 78982-0001-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0003-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0006-01 KLEAN 4 g — — FDA listed —
Loris BZK Antiseptic Wipes .13 g/100g 68356-0126-01 LernaPharm 100 packets — — Discontinued —
McKesson Benzalkonium Chloride Towelette .13 g/100g 68599-5807-03 McKesson 100 packets — — FDA listed —
Zoviro .13 g/100g 83814-0004-01 Zoviro, 80 pouches — — FDA listed —
Antiseptic Towelettes .13 g/100g 49687-0011-01 CMC 10 patches — — FDA listed —
Zoom Wipes .13 g/100g 70401-0150-01 ZOOM 1500 packets — — Discontinued —
Antiseptic Wipe .13 g/100g 71584-0002-01 Guangdong 1.6 g — — FDA listed —
Safly BZK Antiseptic Towelette .13 g/100g 71734-0116-01 JIANGMEN 2 g — — FDA listed —
2XL Mega Rolls Sanitizing Wipes .13 g/100g 71995-0020-01 2xl 2300 packets — — FDA listed —
tazza JIM WIPES .13 g/100g 76370-0039-01 Tazza 1500 patches — — FDA listed —
tazza ECOFIT WIPES .13 g/100g 76370-0040-01 Tazza 1500 patches — — FDA listed —
Biopure Anti-bacterial Hand Wipes Honey Wildflower Scent .13 g/100g 78691-0033-00 Quest 20 g — — FDA listed —
Klean Freak .13 g/100g 78982-0005-01 KLEAN 4 g — — FDA listed —
Klean Freak .13 g/100g 78982-0007-01 KLEAN 4 g — — FDA listed —
Sanitising Wipes .13 g/100g 81331-0001-13 Sportsmith, 800 nots — — Discontinued —
Wet Ones Antibacterial Hand Wipes Lavender Scent .13 g/100g 63354-0536-20 Edgewell 20 g — — FDA listed —
Diamond Wipes Antibacterial Hand Wipes .13 g/100g 64709-0111-10 Diamond 1 g — — FDA listed —
Antibacterial Wet wipes .13 g/100g 73760-0001-01 Zhejiang 15 pouches — — FDA listed —
tazza HAND SANITIZER KING WIPES .13 g/100g 76370-0030-01 Tazza 950 patches — — FDA listed —
MediChoice OB Cleansing .13 g/100g 39892-0306-01 O&M 1000 patches — — FDA listed —
McKesson Obstetrical Antiseptic Towelette .13 g/100g 68599-5806-03 McKesson 100 packets — — FDA listed —
Sanitizing Wipes .13 g/100g 70972-1200-01 Wipes 1200 packets — — FDA listed —
Antibacterial Bandages .13 g/100g 71584-0111-01 Guangdong 5 g — — FDA listed —
Simplify Antibacterial Hand Wipes .13 g/100g 11822-0286-02 RITE 24 patches — — FDA listed —
Antibacterial Hand wipes .13 g/100g 51628-9999-01 MY 12 g — — FDA listed —
Crayola ANTIBACTERIAL HAND WIPES .13 g/100g 70108-0310-01 ASHTEL 20 patches — — FDA listed —
Keep Going Non Sting Cleaning Wipe .13 g/100g 71734-0343-01 JIANGMEN 2 g — — FDA listed —
Go Home And Haven Antibacterial Hand Wipes .13 g/100g 85828-0301-01 Grocery 124 g — — FDA listed —
KeepGoing Non Sting Cleaning Wipe .13 g/100g 82942-1007-01 J&A 5 g — — FDA listed —
24 7 life by 7 Eleven Antibacterial HAND WIPES .13 g/100g 10202-0402-01 7-ELEVEN, 20 patches — — FDA listed —
Alta Antibacterial Hand Wipes .13 g/100gthis 79165-0777-20 Alta 1 packet — — FDA listed —
DrugStore Antibacterial Hand Wipes .13 g/100g 29485-6666-01 Lil' 30 patches — — 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

🏛️
2020
On the market since
Jul 2020
📍
2026
Currently FDA-listed
6 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
79165-0777-20 You're viewing this 20 PACKAGE in 1 PACKET (79165-777-20) / 3.6 g in 1 PACKAGE 2020-07-01 Active
79165-0777-90 90 PACKAGE in 1 PACKET (79165-777-90) / 3.6 g in 1 PACKAGE 2020-07-01 Active

Pack size FAQ

What quantity is in NDC 79165-0777-20?
NDC 79165-0777-20 contains 1 packet — 20 package in 1 packet / 3.6 g in 1 package.
What is the difference between NDC 79165-0777-20 and NDC 79165-0777-90?
Both are ALTA ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE .13 g/100g Cloth — the drug itself is identical. NDC 79165-0777-20 is the 1 packet package, while NDC 79165-0777-90 is the 1 packet package.
What NDC number is used to bill for this package of ALTA ANTIBACTERIAL HAND WIPES BENZALKONIUM CHLORIDE .13 g/100g Cloth?
Bill NDC 79165-0777-20 — the 11-digit billing format is 79165077720. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 79165-777-20, 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: 79165-0777-20, written without dashes as 79165077720. 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 79165-0777-20, the first segment (79165) is the labeler code FDA assigned to Alta Sales Inc; the middle segment (0777) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (20) 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 Alta Sales 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 packet (79165-0777-90). 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?
Alta Sales 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.

📄 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
🎯 Indications and Usage 5 words ▾

Use Decreases bacteria on skin

⏱️ Dosage and Administration 25 words ▾

Directions for use Thoroughly wipe hands and face as desired. Allow to dry without wiping. Discard wipe in trash receptacle after use. Do not flush.

⚠️ Warnings 52 words ▾

Warnings For external use only Keep out of eyes. In case of eye contact, rinse with water. If irritation develops, discontinue use. Consult a doctor if irritation persists more than 72 hours. If swallowed, seek medical attention or contact a Poison Control Center. Keep out of the children, except with adult supervision.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.13%

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients Aqua, Phenoxyethanol, Perfume, Propylene Glycol, Cocamidopropyl Betaine, PEG-7 Glyceryl Cocoate, Benzoic acid, Tetrasodium Edta, Dehydroacetic acid, Glycerin, Polysorbate 20, Citric acid

🎯 Purpose 2 words ▾

Purpose Antibacterial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 79163-0399-02 · Eco 79184-0042-01 · Sichuan →
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.