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KeepGoing Non Sting Cleaning Wipe benzalkonium chloride .13 g/100g Swab, 5 g — NDC 82942-1007-01 package photo

KeepGoing Non Sting Cleaning Wipe benzalkonium chloride .13 g/100g Swab, 5 g

by J&A Digital Inc. · 5 g in 1 PACKAGE (82942-1007-1)
NDC 82942-1007-01
🏷️ FDA NDC (as labeled) 82942-1007-1 billing pads the package segment with a zero
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) 82942-1007-1
Product NDC 82942-1007
11-digit billing NDC 82942100701
RxCUI 1038558
UNII F5UM2KM3W7
Application # M003
SPL Set ID 1a6303ce-8df7-4e8b-93f2-e162fdd2540c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-15
Route TOPICAL
Dosage form SWAB
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 82942-1007-1 — 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 → 82942-1007-01. 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.

🏭 Manufacturer & labeler

LabelerJ&A Digital Inc.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code82942
First marketedJul 2026
Product typeHuman Otc Drug
Portfolio7 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

🧪 What is this product?

KeepGoing Non Sting Cleaning Wipe is a topical antiseptic swab containing benzalkonium chloride, an antimicrobial agent commonly used to reduce bacteria on the skin. This over-the-counter monograph product is formulated as a pre-moistened wipe for topical application. Benzalkonium chloride functions as a surface disinfectant and is typically used for skin cleansing and minor wound care before medical procedures or to help prevent infection in minor cuts and scrapes.

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 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.

1 inactive ingredient listed in the exact product block matched to this NDC.

The official label also statesPurified 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.

💲 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.
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/100gthis 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/100g 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

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

🔬 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 KeepGoing Non Sting Cleaning Wipe (this brand).

Top reported reactions

Drug Hypersensitivity118
Condition Aggravated114
Arthralgia112
Musculoskeletal Stiffness111
Pain In Extremity111
Infection110
Hepatotoxicity108

Age at onset

Infant1
Adolescent3
Adult36
Elderly10

Reporter sex

331 reports
Male · 28%
Female · 72%
Unknown · 0%

Serious outcomes

Death25
Disabling18
Reports over time (by year) — tap or hover for the count & year
2023 2024 2025 2026 24 5
Most recent year is provisional (FAERS lags ~3 months).
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
82942-1007-01 You're viewing this 5 g in 1 PACKAGE (82942-1007-1) 2026-07-15 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 ✓ 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 82942-1007-1, 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: 82942-1007-01, written without dashes as 82942100701. 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 82942-1007-01, the first segment (82942) is the labeler code FDA assigned to J&A Digital Inc.; the middle segment (1007) 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 J&A Digital Inc.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
J&A Digital 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 16 words ▾

Uses: First aid to help decrease the risk of infection in minor cuts, scrapes, and burns.

⏱️ Dosage and Administration 10 words ▾

Directions Gently wipe wound and/or surrounding skin. Discard after use.

⚠️ Warnings 83 words ▾

Warnings For external use only. Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor. Stop use and ask a doctor if the condition persists or gets worse. Do not use longer than 1 week unless directed by a doctor. Keep out of reach of children. Keep out of reach of children. If swallowed get medical help or contact a Posion Control Center immediately.

🧪 Active Ingredient 7 words ▾

Active Ingredient Benzalkonium Chloride .......... 0.13 %

🧪 Inactive Ingredients 4 words ▾

Inactive Ingredients: Purified Water

🎯 Purpose 4 words ▾

Purpose First Aid Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 82942-1006-01 · J&A 82944-0100-10 · Ion →
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.