Home › NDC Lookup › Ingredients › Benzalkonium Chloride › 68041-0519-00
Chemcor Chemical Foaming Hand Sanitizer Benzalkonium Chloride .0013 mg/mL Liquid — NDC 68041-0519-00 package photo

Chemcor Chemical Foaming Hand Sanitizer Benzalkonium Chloride .0013 mg/mL Liquid

by Chemcor Chemical Corporation · 4 BOTTLE in 1 BOX (68041-519-00) / 3785 mL in 1 BOTTLE (68041-519-01)
NDC 68041-0519-00
🏷️ FDA NDC (as labeled) 68041-519-00 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ Data synced 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

⚠️
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-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

🆔 Identity & classification

FDA NDC (as labeled) 68041-519-00
Product NDC 68041-519
11-digit billing NDC 68041051900
RxCUI 1049254
UNII F5UM2KM3W7
Application # M
SPL Set ID 5c9d90c1-0381-4237-9529-398fa51b3ab4
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-01
Route TOPICAL
Dosage form LIQUID
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 68041-519-00 — 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 → 68041-0519-00. 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

LabelerChemcor Chemical Corporation
FDA applicationM (OTC MONOGRAPH DRUG)
Labeler code68041
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio4 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?

This is a topical foaming hand sanitizer marketed as an over-the-counter monograph product. It contains benzalkonium chloride, an antimicrobial ingredient that is commonly used in sanitizers and disinfectants to help reduce bacteria on skin. The product is applied by hand and is intended for routine hand hygiene purposes. As an OTC monograph drug, it is manufactured according to FDA category standards rather than as an individually approved application.

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 LVX2APC4XR
    A synthetic organic compound used as a humectant and solvent in medicines. It helps retain moisture in formulations and improve the texture and spreadability of topical products.
  • 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 H2KVQ74JM4
    A compound derived from coconut oil that acts as a conditioning agent and surfactant. It helps stabilize and thicken liquid formulations while reducing static and improving texture in topical products.
  • UNII 8AR51R3BL5
    A cleaning agent derived from coconut oil, used as a surfactant and emulsifier to help mix oil and water-based ingredients together in liquid formulations.
  • 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.

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

The official label also statesWater, Cocamidopropyl PG-dimonium Chloride Phosphate, Dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, 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 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.
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
Walgreens Advanced Wound Wash 1.3 mg/mL 00363-9656-10 Walgreens 1 bottle — — FDA listed —
HUMCO Merthiolate 1.3 mg/mL 00395-8010-92 Humco 59 ml — — FDA listed —
Bak 1 750 .1713 g/100mL 12745-0145-01 Medical 473 ml — — FDA listed —
Tincture Merthiolate 1.3 mg/mL 24286-1532-07 DLC 30 ml — — FDA listed —
Puri-San Plus Instant Hand Sanitizer 1.3 mg/mL 43097-0457-10 People's 1000 ml — — Discontinued —
United Airlines .13 g/100mL 52305-0601-25 Freshorize 250 ml — — FDA listed —
Alaska Airlines .13 g/100mL 52305-0602-30 Freshorize 250 ml — — FDA listed —
El Valle Merthiolate 1.3 mg/mL 55758-0375-02 Pharmadel 30 ml — — FDA listed —
safeHands Hand Sanitizer Fragrance Free .13 g/100mL 60867-0150-02 Safehands 52 ml — — FDA listed —
safeHands Hand Sanitizer Clean Linen .13 g/100mL 60867-0152-02 Safehands 52 ml — — FDA listed —
QS Plus Plus Instant Hand Sanitizer 1.3 mg/mL 62257-0457-10 ABC 1000 ml — — Discontinued —
RELEEV Cold Sore Treatment 1.3 mg/mL 63287-0419-01 Merix 1 pouch — — FDA listed —
Quality Choice Merthiolate 1.3 mg/mL 63868-0493-02 Chain 59 ml — — FDA listed —
Soft Care Instant Hand Sanitizer AF .13 g/100mL 64536-3628-03 Diversey, 1300 ml — — FDA listed —
Bactine Max .13 g/100mL 65197-0820-80 WellSpring 1 bottle — — FDA listed —
Cold Sore Treatment, 24-7 Life by 7-Eleven 1.3 mg/mL 66715-5189-00 Lil' 1 bottle — — FDA listed —
Novex Hand Sanitizer 1.3 mg/mL 66902-0037-25 Natural 225 ml — — FDA listed —
Chemcor Chemical Foaming Hand Sanitizer .0013 mg/mLthis 68041-0519-00 Chemcor 4 bottles — — FDA listed —
Antimicrobial 1.3 ug/mg 68599-0214-04 McKesson 118 mg — — FDA listed —
Zoono Hand Sanitizer .13 g/100mL 69221-0203-11 Zoono 50 ml — — FDA listed —
Zoono Alcohol Free Hand Sanitizer .13 g/100mL 69221-0601-11 Zoono 50 ml — — FDA listed —
CVS Merthiolate 1.3 mg/mL 69842-0749-92 CVS 59 ml — — FDA listed —
ElimiShield Home and Outdoor Moisturizing Hand Sanitizer 1.3 mg/mL 71853-0006-01 Bryson 50 ml — — FDA listed —
U Hand Sanitizer Classic .13 g/100mL 72119-0004-01 BLUE 100 ml — — FDA listed —
Mercurochrome First Aid Antiseptic 1.3 mg/mL 73635-1223-01 Germa 30 ml — — Discontinued —
Merthiolate Tincture First Aid Antiseptic 1.3 mg/mL 73635-1224-01 Germa 30 ml — — Discontinued —
tazza HAND SANITIZER .13 g/.1L 76370-0032-00 Tazza 3.78 l — — FDA listed —
tazza Alcohol-Free sanitizer .13 g/.1L 76370-0041-00 Tazza 1 l — — FDA listed —
Hygiene Clean Clean Cotton Hand Sanitizer 1.3 mg/mL 80499-0001-01 USA 237 ml — — FDA listed —
Hygiene Clean Eucalyptus Hand Sanitizer 1.3 mg/mL 80499-0002-01 USA 237 ml — — FDA listed —
Hygiene Clean Unscented Hand Sanitizer 1.3 mg/mL 80499-0003-01 USA 237 ml — — FDA listed —
Hygiene Clean Pumpkin Spice Hand Sanitizer 1.3 mg/mL 80499-0008-01 USA 50 ml — — FDA listed —
Hygiene Clean Blueberry Lemonade Hand Sanitizer 1.3 mg/mL 80499-0009-01 USA 50 ml — — FDA listed —
Hygiene Clean Leather Oak Hand Sanitizer 1.3 mg/mL 80499-0010-01 USA 50 ml — — FDA listed —
Hygiene Clean Mahogany Teakwood Hand Sanitizer 1.3 mg/mL 80499-0011-01 USA 50 ml — — FDA listed —
Hygiene Clean Bubble Gum Hand Sanitizer 1.3 mg/mL 80499-0012-01 USA 50 ml — — FDA listed —
Hygiene Clean Eucalyptus Hand Sanitizer 1.3 mg/mL 80499-0013-01 USA 50 ml — — FDA listed —
Hygiene Clean Unscented Clean Hand Sanitizer 1.3 mg/mL 80499-0014-01 USA 50 ml — — FDA listed —
Hygiene Clean Balsam Fir Hand Sanitizer 1.3 mg/mL 80499-0015-01 USA 50 ml — — FDA listed —
Hygiene Clean Blueberry Lemonade Hand Sanitizer Car Safe Alcohol-Free 1.3 mg/mL 80499-0017-00 USA 237 ml — — FDA listed —
Hygiene Clean Vanilla Woods Hand Sanitizer Car Safe Alcohol Free 1.3 mg/mL 80499-0018-00 USA 237 ml — — FDA listed —
Hygiene Clean Vanilla Sugar Hand Sanitizer on the go and car safe 1.3 mg/mL 80499-0030-01 USA 50 ml — — FDA listed —
Hygiene Clean Luxury Clean hand Sanitizer on the go and car safe 1.3 mg/mL 80499-0031-01 USA 50 ml — — FDA listed —
Hygiene Clean Lavender Blossom Hand Sanitizer 1.3 mg/mL 80499-0103-01 USA 50 ml — — FDA listed —
Hygiene Clean Lilac Garden Hand Sanitizer 1.3 mg/mL 80499-0104-01 USA 50 ml — — FDA listed —
Hygiene Clean Spring Bloom Hand Sanitizer 1.3 mg/mL 80499-0105-01 USA 50 ml — — FDA listed —
Purifi Hand Sanitizer .13 g/100mL 80659-0301-01 Purifi 250 ml — — FDA listed —
Merthiolate 1.3 mg/mL 82645-0912-92 Pharma 59 ml — — FDA listed —
Caseys .13 g/100g 85844-0001-01 Zhejiang 15 patches — — FDA listed —
Foaming Antibacterial Handsoap .0013 mg/mL 68041-0512-01 Chemcor 3780 ml — — FDA listed —
Victoria Bay Antimicrobial Foam Handwash 1200 mL .0013 mg/mL 71907-0114-40 Dade 1200 ml — — FDA listed —
PURELL HEALTHY SP BAK E2 Antimicrobial Foam Sp .0013 mg/mL 21749-0113-40 GOJO 2000 ml — — FDA listed —
Reliable Brand Powered by PURELL Antimicrobial Fragrance Free Foam CB10 1.2L .0013 mg/mL 71897-0114-40 Veritiv 1200 ml — — FDA listed —
GOJO E2 Foam Handwash with BAK .0013 mg/mL 21749-0112-20 GOJO 2000 ml — — FDA listed —
RENOWN RB10 1200 ML Antibacterial Foam Hand SP .0013 mg/mL 42584-0401-01 Home 1200 ml — — FDA listed —
Hawthorn Hygiene Solutions ENERGY ANTIBACTERIAL FOAM FRAGRANCE FREE 1200 mL .0013 mg/mL 66294-0114-40 BUNZL 1200 ml — — 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
Jun 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.

🔬 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 Chemcor Chemical Foaming Hand Sanitizer (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

Hospitalization175
Life-threatening27
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
68041-0519-00 You're viewing this 4 BOTTLE in 1 BOX (68041-519-00) / 3785 mL in 1 BOTTLE (68041-519-01) 2020-06-01 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 68041-519-00, 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: 68041-0519-00, written without dashes as 68041051900. 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 68041-0519-00, the first segment (68041) is the labeler code FDA assigned to Chemcor Chemical Corporation; the middle segment (0519) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (00) 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 Chemcor Chemical Corporation. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
Chemcor Chemical Corporation 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 14 words ▾

Uses For hand sanitizing to decrease bacteria on the skin Recommended for repeated use

⏱️ Dosage and Administration 25 words ▾

Directions Pump a small amount of foam into palm of hand Rub thoroughly over all surfaces of both hands Rub hands together briskly until dry

⚠️ Warnings 61 words ▾

Warnings For external use only When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.1%

🧪 Inactive Ingredients 13 words ▾

Inactive Ingredients Water, Cocamidopropyl PG-dimonium Chloride Phosphate, Dihydroxyethyl cocamine oxide, acetamidoethoxyethanol, citric acid.

🎯 Purpose 2 words ▾

Purpose Antimicrobial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 68041-0512-01 · Chemcor 68041-0604-01 · Chemcor →
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.