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HACCP QE2 Benzalkonium Chloride 1200 ug/mL Liquid, 3785 mL — NDC 59900-0718-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

HACCP QE2 Benzalkonium Chloride 1200 ug/mL Liquid, 3785 mL — NDC 59900-718-03 (Billing 59900-0718-03)

by Best Sanitizers, Inc · 3785 mL in 1 JUG

This is a package of 3,785 mL of HACCP QE2 Benzalkonium Chloride 1200 ug/mL Liquid from Best Sanitizers, Inc, marketed since Jul 2014 and currently FDA-listed.

NDC 59900-0718-03
🏷️ FDA NDC (as labeled) 59900-718-03 billing pads the product segment with a zero
This package
Contains3785 mL Pack sizes3 compare ↓
Product page 59900-0718-01 Also comes in: 1000 ml 59900-718-02 1200 ml 59900-718-01
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

NDC database record

One package, one record: these facts belong to NDC 59900-718-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
59900 labeler · 718 product · 03 package
Package marketed since
Jul 16, 2014
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 5990071803 5
FDA record last changed
Jul 24, 2026
⚠️
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

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 59900-718-03
Product NDC 59900-718
11-digit billing NDC 59900071803
RxCUI 1053188
UNII F5UM2KM3W7
Application # 505G(a)(3)
SPL Set ID 0b861f72-f93e-40d6-9967-43e5f6b7c128
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2014-07-16
Route TOPICAL
Dosage form LIQUID
Substance BENZALKONIUM CHLORIDE
Quick answers
  • RxCUI (RxNorm): 1053188
Why two NDCs? The FDA registers this code as 59900-718-03 — 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 → 59900-0718-03. 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.

Clinical

🧪 What is this product?

HACCP QE2 is a topical liquid containing benzalkonium chloride, an antimicrobial agent commonly used in over-the-counter antiseptic and disinfectant products. This product is marketed under FDA's OTC monograph rules for its category rather than as an individually approved drug application. Benzalkonium chloride typically functions as a broad-spectrum antimicrobial to help reduce bacteria on skin and surfaces. The liquid form is applied directly to the area being treated.

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: 1000 ml 1200 ml
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
59900-0718-01 59900-718-01 Main listing 1200 mL in 1 BOTTLE 2014-07-16 — Active
59900-0718-02 59900-718-02 1000 mL in 1 BAG 2014-07-16 — Active
59900-0718-03 You're viewing this 3785 mL in 1 JUG 2014-07-16 — Active

You're viewing the largest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 3785 mL — 3785 ml in 1 jug.
How does this package differ from NDC 59900-0718-02?
Both are HACCP QE2 Benzalkonium Chloride 1200 ug/mL Liquid — the drug itself is identical. This page's package is the 3785 mL one, while NDC 59900-0718-02 is the 1000 ml package.
What NDC number is used to bill for this package of HACCP QE2 Benzalkonium Chloride 1200 ug/mL 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
Safeguard Antibacterial Foaming .12 g/100mL 37000-0601-40 The 1200 ml — — FDA listed —
Safeguard Antibacterial E2 Foaming .12 g/100mL 37000-0602-40 The 1200 ml — — FDA listed —
Alpet Q E2 1.2 g/1000mL 59900-0130-01 Best 1250 ml — — FDA listed —
Alpet Qe2 Sanitizing Foam 1.2 mg/mL 59900-0214-01 Best 946352 ml — — FDA listed —
HACCP Q E2 Sanitizing 1.2 mg/mL 59900-0215-01 Best 946352 ml — — FDA listed —
Haccp Qe2 1200 ug/mLthis 59900-0718-03 Best 3785 ml — — FDA listed —
Total Solutions Hygien Hand .12 g/100mL 62819-0268-01 Athea 3785 ml — — FDA listed —
Alpha E2 Pro-Q Sanitizing Foam 1.2 g/1000mL 69335-0004-02 Alpha 1250 ml — — FDA listed —
San X E2 .12 g/100mL 69884-0706-06 Amerisan, 1250 ml — — FDA listed —
Avance Incontinence Care .12 g/100g 70936-0112-08 SMART 237 g — — FDA listed —
Chemstation HACCP Q E2 1.2 g/L 71212-0101-00 ChemStation 208.198 l — — FDA listed —
Chemstation Q E2 1.2 g/L 71212-0102-00 Chemstation 208.198 l — — 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

🏛️
2014
On the market since
Jul 2014
📍
2026
Currently FDA-listed
12 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.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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

LabelerBest Sanitizers, Inc
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code59900
First marketedJul 2014
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Best Sanitizers, Inc labeler code 59900

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 📄 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 29 words ▾

Uses handwash to help reduce bacteria that potentially can cause disease helps to prevent cross-contamination by hand contact helps to prevent drying of the skin recommended for repeated use

⏱️ Dosage and Administration 43 words ▾

Directions wet hands and wrists with clean, running water apply appropriate amount of product lather and scrub hands, fingers, fingernails, cuticles and wrists for at least 20 seconds rinse thoroughly with running water dry hands completely (incomplete drying may result in chapped skin)

⚠️ Warnings 5 words ▾

Warnings For external use only

📦 Storage and Handling 13 words ▾

Other information store in a cool dry place below 104° F (40° C)

🧪 Active Ingredient 6 words ▾

Active ingredient Benzalkonium Chloride 0.12% w/w

🧪 Inactive Ingredients 20 words ▾

Inactive ingredients Water, cocamidopropyl betaine, C12-14 amine oxides, 1,2-propanediol, glycerol, guar gum, xanthan gum, benzyl alcohol, dehydroacetic acid, tetra-sodium EDTA

🎯 Purpose 4 words ▾

Purpose Antiseptic Hand Cleanser

📄 When Using This Product 11 words ▾

When using this product do not use in or near eyes.

📄 Stop Use and Ask a Doctor If 11 words ▾

Stop use and ask a doctor if irritation and redness develop.

📄 Keep Out of Reach of Children 18 words ▾

Keep out of reach of children. If swallowed, seek medical attention or contact a Poison Control Center immediately.

📄 Questions or Comments 11 words ▾

Questions? Contact Best Sanitizers at 888-225-3267 Mon-Fri 9am - 4pm PST

📄 Package Label / Principal Display Panel 37 words ▾

BEST SANITIZERS INC. HACCP QE2 Sanitizing Liquid Soap NSF [Nonfood Compounds Program Listed (E2) Registration #149724] 0.12% Benzalkonium Chloride (BAC) formula Rich, thick lather FOR FOOD INDUSTRY PROFESSIONALS Net Contents: 1 U.S. Gallon (3.78 liters) 59900-718 new

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) — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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 Best Sanitizers, 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 2 other package presentations of this same product, including 1000 ml (59900-0718-02), 1200 ml (59900-0718-01). 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?
Best Sanitizers, 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.
← 59900-0352-01 · Best 59900-0757-01 · Best →
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.