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Antimicrobial Hand So ap Chloroxylenol .003 mg/mL Liquid, 2000 mL — NDC 61666-003-67 (Billing 61666-0003-67)

by Waxie Sanitary Supply · 2000 mL in 1 PACKAGE

This is a package of 2,000 mL of Antimicrobial Hand So ap Chloroxylenol .003 mg/mL Liquid from Waxie Sanitary Supply, no longer marketed (first marketed Jan 2003), no longer in the FDA NDC Directory.

NDC 61666-0003-67
🏷️ FDA NDC (as labeled) 61666-003-67 billing pads the product segment with a zero
This package
Contains2000 mL Pack sizes2 compare ↓
Product page 61666-0003-42 Also comes in: 1250 ml 61666-003-42
OTC Discontinued Non-controlled ⚠ Discontinued by firm ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 61666-003-67 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
61666 labeler · 003 product · 67 package
Barcode (UPC-A, from the NDC)
3 6166600367 6
FDA record last changed
Jul 24, 2026
⚠️
Excluded from the active FDA NDC Directory. The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. The listing was last certified through Sep 2026. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory. Search the FDA NDC Directory ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 61666-003-67
Product NDC 61666-003
11-digit billing NDC 61666000367
UNII 0F32U78V2Q
Application # M505G(a)(3)
SPL Set ID 73fd1b9e-4a27-4bb8-8e97-6cc08459597f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status Discontinued
FDA listing status Discontinued by firm (certified through Sep 2026)
Marketing start 2003-01-01
Marketing end 2026-09-01
Route TOPICAL
Dosage form LIQUID
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 61666-003-67 — 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 → 61666-0003-67. 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

🧪 What is this product?

This is a topical antimicrobial hand soap liquid containing chloroxylenol. Chloroxylenol is commonly used in over-the-counter hand cleansing products as an antimicrobial agent to help reduce certain bacteria and microorganisms on the skin. As an OTC monograph drug, this product is marketed under FDA rules established for this category of cleansers rather than through an individual application review. Hand soaps containing chloroxylenol are typically used during routine handwashing.

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: 1250 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
61666-0003-42 61666-003-42 Main listing 1250 mL in 1 PACKAGE 2003-01-01 Sep 1, 2026 Discontinued by firm
61666-0003-67 You're viewing this 2000 mL in 1 PACKAGE 2003-01-01 — Discontinued by firm

You're viewing the largest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 2000 mL — 2000 ml in 1 package.
How does this package differ from NDC 61666-0003-42?
Both are Antimicrobial Hand So ap Chloroxylenol .003 mg/mL Liquid — the drug itself is identical. This page's package is the 2000 mL one, while NDC 61666-0003-42 is the 1250 ml package.
What NDC number is used to bill for this package of Antimicrobial Hand So ap Chloroxylenol .003 mg/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
Luxury Foam Antibacterial .003 mg/mL 21749-0080-42 GOJO 1250 ml — — FDA listed —
GOJO PCMX E-2 Sanitizing Ltn Sp .003 mg/mL 21749-0457-20 GOJO 2000 ml — — FDA listed —
Antimicrobial Hand So ap .003 mg/mLthis 61666-0003-67 Waxie 2000 ml — — Discontinued —
PRO-LINK Free Hands Antibacterial Foam So ap .003 mg/mL 66908-0081-40 Pro-Link, 1200 ml — — FDA listed —
GOJO Gold and Klean Antimicrobial Ltn Sp .003 mg/mL 21749-0501-80 GOJO 800 ml — — FDA listed —
BRIGHTON PROFESSIONAL Antibacterial Foaming Hand So ap .003 mg/mL 49514-0080-42 Staples 1250 ml — — FDA listed —
BRIGHT SOLUTIONS Antimicrobial Foam So ap .003 mg/mL 66885-0081-40 Kel-San, 1200 ml — — FDA listed —
EXTENDED CARE Foaming Antimicrobial Handwash .003 mg/mL 71875-0080-42 TRIPLE 1250 ml — — FDA listed —
RENOWN Antibacterial Foam Cleanser .003 mg/mL 71896-0081-42 Interline 1250 ml — — FDA listed —
QSC Foam Fresh Antimicrobial Hand .003 mg/mL 59110-0081-42 Triple 1250 ml — — FDA listed —
WAXIECARE Pink Antibacterial Ltion So ap .003 mg/mL 61666-0004-67 Waxie 2000 ml — — FDA listed —
DON Luxury Foam Antibacterial Handwash .003 mg/mL 66910-0600-42 Edward 1250 ml — — FDA listed —
Premium Foam Antibacterial .003 mg/mL 21749-0085-23 GOJO 222 ml — — FDA listed —
PRIMORY Antimicrobial Foam .003 mg/mL 21749-0555-43 GOJO 1500 ml — — Discontinued —
MICRELL Antibacterial Ltn Sp .003 mg/mL 21749-0975-04 GOJO 118 ml — — Discontinued —
GRAND TOUCH Antimicrobial Ltion So ap .003 mg/mL 61666-0007-34 Waxie 1000 ml — — Discontinued —
GENUINE JOE Cleaning Supplies Antibacterial Foam So ap Refill .003 mg/mL 62832-0080-42 S.P. 1250 ml — — FDA listed —
PROVON Foaming Antimicrobial Handwash with Moisturizers .003 mg/mL 21749-0090-22 GOJO 200 ml — — Discontinued —
ACQUAINT Antibacterial Foam Handwash .003 mg/mL 21749-0551-90 GOJO 1250 ml — — FDA listed —
TOUGH GUY Antibacterial Foam Hand So ap .003 mg/mL 40096-0081-01 W.W. 1200 ml — — FDA listed —
GOJO Antibacterial Ltn Sp .003 mg/mL 21749-0458-37 GOJO 3780 ml — — FDA listed —
PROVON Antimicrobial Ltn Sp with 0.3% PCMX .003 mg/mL 21749-0750-04 GOJO 118 ml — — FDA listed —
Southern Soft Luxury Foam Antibacterial Hand Wash .003 mg/mL 53341-0080-42 CCP 1250 ml — — FDA listed —
Antimicrobial Foam So ap with PCMX .003 mg/mL 61666-0005-40 Waxie 1200 ml — — FDA listed —
PRIME SOURCE Antimicrobial Foam So ap .003 mg/mL 66294-0082-40 BUNZL 1200 ml — — FDA listed —
Reliable Luxury Foam Antimicrobial Handwash Fresh Fruit Scent .003 mg/mL 71897-0080-40 Veritiv 1200 ml — — FDA listed —
EXCELON Antimicrobial Foam .003 mg/mL 21749-0580-43 GOJO 1500 ml — — Discontinued —
SIGNATRY Antimicrobial Foam .003 mg/mL 21749-0581-43 GOJO 1500 ml — — Discontinued —
TOUGH GUY 821 Antimicrobial Liquid Ltion So ap .003 mg/mL 40096-0051-01 W.W. 3780 ml — — FDA listed —
TOUGH GUY Antimicrobial Foam So ap .003 mg/mL 40096-0080-05 W.W. 1250 ml — — FDA listed —
AFFEX Foaming Antimicrobial Hand So ap .003 mg/mL 54057-0083-42 Afflink, 1250 ml — — FDA listed —
BRIGHT SOLUTIONS Foaming Antimicrobial So ap .003 mg/mL 66885-0080-42 Kel-San, 1250 ml — — FDA listed —
RENOWN Antimicrobial So ap .003 mg/mL 71896-0051-27 Interline 800 ml — — Discontinued —
BRIGHTON PROFESSIONAL Premium Antibacterial Foam So ap .003 mg/mL 49514-0081-40 Staples 1200 ml — — FDA listed —
BOARDWALK Antibacterial Foam Handwash .003 mg/mL 71906-0080-42 Essendant 1250 ml — — FDA listed —
QSC TF Ambre Antibacterial Wash .003 mg/mL 59110-0082-40 Triple 1200 ml — — FDA listed —
GOJO RICH PINK Antibacterial Ltn Sp .003 mg/mL 21749-0060-20 GOJO 2000 ml — — FDA listed —
GOJO Ultra Mild Antimicrobial Ltn Sp with Chloroxylenol .003 mg/mL 21749-0211-10 GOJO 1000 ml — — Discontinued —
COMPANIONS Luxury Foam Hand So ap, Antimicrobial .003 mg/mL 24205-0080-42 UniPro 1250 ml — — FDA listed —
ARRAY Anitbacterial Foam Handwash .003 mg/mL 52220-0080-40 Gordon 1200 ml — — Discontinued —
AFFEX Antimicrobial Foaming Hand So ap .003 mg/mL 54057-0082-42 Afflink, 1250 ml — — FDA listed —
PRIME SOURCE Antimicrobial Foaming Hand So ap .003 mg/mL 66294-0080-42 BUNZL 1250 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

🏛️
2003
On the market since
Jan 2003
📍
2026
Currently FDA-listed
23 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.

We could not link this NDC to a current FDA Structured Product Label. An inactive-ingredient list is therefore not available from this source.
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

LabelerWaxie Sanitary Supply
FDA applicationM505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code61666
First marketedJan 2003
Product typeHuman Otc Drug
Portfolio5 products on file

More NDCs from Waxie Sanitary Supply labeler code 61666

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 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 13 words ▾

Uses Handwash to help decrease bacteria on the skin Recommended for repeated use

⏱️ Dosage and Administration 20 words ▾

Directions Wet hands Apply a small amount of product and work into a lather Rinse well and dry hands completely

⚠️ Warnings 58 words ▾

Warnings For external use only When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation or rash appears and lasts Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 4 words ▾

Active ingredient Chloroxylenol 0.3%

🧪 Inactive Ingredients 51 words ▾

Inactive ingredients Water (Aqua), Alcohol, Ammonium Laureth Sulfate, Ammonium Lauryl Sulfate, Propylene Glycol, Ammonium Xylenesulfonate, Cocamide MEA, Glycerin, Isopropyl Alcohol, Lactic Acid, Retinyl Palmitate, Simmondsia Chinensis (Jojoba) Seed Oil, Tetrasodium EDTA, Tocopheryl Acetate, Zea Mays (Corn) Oil, Ammonium Sulfate, Fragrance (Parfum), Methylchloroisothiazolinone, Methylisothiazolinone, Red 4 (CI 14700), Yellow 6 (CI 15985)

🎯 Purpose 2 words ▾

Purpose Antimicrobial

📄 When Using This Product 21 words ▾

When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water.

📄 Stop Use and Ask a Doctor If 13 words ▾

Stop use and ask a doctor if irritation or rash appears and lasts

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel 2 words ▾

Product label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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 Chloroxylenol — the ingredient across all brands.

Top reported reactions

Nausea9
Vomiting9
Pain8
Erythema7
Malaise7
Renal Failure7
Weight Decreased7

Reporter sex

0 reports

Serious outcomes

Death9
Disabling1
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 10 0
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.

About this NDC listing & data coverage

Over-the-counter (OTC) product No longer marketed (per FDA listing data)
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 — Not published for this NDC No photo available yet for this listing.
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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.
Does this product come in other package sizes?
Yes — the FDA directory lists 1 other package presentation of this same product, including 1250 ml (61666-0003-42). 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?
Waxie Sanitary Supply 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.
← 61662-0022-01 · Lianyungang 61666-0004-67 · Waxie →
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.