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Ecolab Chloroxylenol 5.2 mg/mL Solution, 750 mL — NDC 47593-0501-41 package photo

Ecolab Chloroxylenol 5.2 mg/mL Solution, 750 mL

by Ecolab Inc. · 750 mL in 1 BOTTLE, PLASTIC (47593-501-41)
NDC 47593-0501-41
🏷️ FDA NDC (as labeled) 47593-501-41 billing pads the product segment with a zero
This package
Contains750 mL Pack sizes7 compare ↓
Also comes in: 540 ml 47593-0501-31 1000 ml 47593-0501-26 1000 ml 47593-0501-32 1200 ml 47593-0501-56 1250 ml 47593-0501-59 3780 ml 47593-0501-11
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

🆔 Identity & classification

FDA NDC (as labeled) 47593-501-41
Product NDC 47593-501
11-digit billing NDC 47593050141
RxCUI 436367
UNII 0F32U78V2Q
UPC 0025469009876
Application # 505G(a)(3)
SPL Set ID b4493ad6-e1c8-4b2d-8a57-1845589b04f9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2012-10-24
Route TOPICAL
Dosage form SOLUTION
Substance CHLOROXYLENOL
Why two NDCs? The FDA registers this code as 47593-501-41 — 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 → 47593-0501-41. 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 Phenol and derivatives class.

Drug family (ATC) Phenol and derivatives
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

LabelerEcolab Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code47593
First marketedOct 2012
Product typeHuman Otc Drug
Portfolio115 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?

Ecolab Chloroxylenol 5.2 mg/mL Solution is a topical liquid product containing chloroxylenol, an antimicrobial ingredient. Chloroxylenol is typically used in skin-cleansing and disinfectant products to reduce bacteria and other microorganisms on the skin surface. This product is an over-the-counter monograph drug, meaning it is marketed under the FDA's established rulebook for antiseptic and antimicrobial skin cleansers rather than as an individually reviewed application.

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.

🧪 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 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 ICS790225B
    A plant-derived cleaning agent made from coconut oil and glucose. It works as a surfactant and emulsifier to help mix oil and water-based ingredients together in the formulation.
  • UNII 9DBA0SBB0L
    A synthetic red dye derived from coal tar used as a colorant in medicines and cosmetics. It gives tablets, capsules, and liquids their red or pink appearance for identification and visual appeal.
  • 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 WZB9127XOA
    A synthetic red dye used to color medications and make them easier to identify. It serves as a colorant in tablets, capsules, and liquid formulations.
  • UNII I753WB2F1M
    FD&C Yellow No. 5 is a synthetic yellow colorant approved by the FDA. It is added to medicines to make pills, tablets, or liquids visually distinct and easier to identify.
  • 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 4PC054V79P
    A fatty acid derived from glycerin and oleic acid (a natural oil component). It acts as an emulsifier to help mix oil and water-based ingredients, and serves as a lubricant and surfactant in the formulation.
  • UNII KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • UNII 7Q6P4JN1QT
    Hydroxyethyl cellulose is a plant-derived thickening agent made from cellulose, a natural fiber. In medications, it acts as a binder and thickener to hold ingredients together and control the product's consistency and flow.
  • UNII DEL7T5QRPN
    A synthetic preservative that kills bacteria and fungi. It's added to medications to prevent microbial growth and extend shelf life, especially in liquid or topical formulations.
  • UNII 229D0E1QFA
    Methylisothiazolinone is a synthetic chemical preservative that prevents bacterial and fungal growth in liquid medicines and topical products. It helps keep the medication safe and extends shelf life during storage.
  • UNII F8U72V8ZXP
    Potassium cocoate is a salt derived from coconut oil. It acts as a surfactant and emulsifier in medicines, helping to mix oil and water-based ingredients together and improve the product's texture and stability.
  • UNII 368GB5141J
    A detergent and foaming agent derived from coconut or palm oil. In medications, it helps break down and mix oil and water-based ingredients, aids in tablet disintegration, and improves how the drug dissolves and spreads in the mouth or digestive system.
  • UNII 0YPR65R21J
    Sodium sulfate is a mineral salt used in pharmaceuticals as a filler and diluent. It helps provide bulk and stability to tablets and capsules while remaining inert in the body.
  • 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.

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

The official label also statesInactive ingredients   water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerin, cocoglucoside, glyceryl oleate, citric acid, frangrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C red #40, FD&C yellow #5, D&C red #33

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.
Try another pack size: 540 ml 1000 ml 1000 ml 1200 ml 1250 ml 3780 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
MICRELL Antibacterial Foam Handwash .005 mg/mL 21749-0095-22 GOJO 200 ml — — Discontinued —
GOJO Antimicrobial Foam Handwash with PCMX .005 mg/mL 21749-0521-53 GOJO 535 ml — — Discontinued —
PROVON Foaming Antimicrobial Handwash with PCMX .005 mg/mL 21749-0541-20 GOJO 2000 ml — — Discontinued —
Ecolab Keystone 5 mg/mL 47593-0465-25 Ecolab 800 ml — — FDA listed —
Ecolab 5.2 mg/mLthis 47593-0501-41 Ecolab 750 ml — — FDA listed —
Ecolab Inc. 5 mg/mL 47593-0503-41 Ecolab 750 ml — — Discontinued —
Ecolab Clean Force 5 mg/mL 47593-0515-25 Ecolab 800 ml — — FDA listed —
Members Mark 5 mg/mL 47593-0573-11 Ecolab 3780 ml — — FDA listed —
Kay Foaming Antibacterial Handsoap PLUS 5 mg/mL 47593-0659-70 Ecolab 1200 ml — — FDA listed —
McD Foaming Antibacterial Handsoap 5 mg/mL 47593-0669-59 Ecolab 1250 ml — — FDA listed —
Kay QSR Antibacterial Handsoap 5 mg/mL 47593-0671-11 Ecolab 3800 ml — — FDA listed —
Qsr Foaming Antibacterial Handsoap 5 mg/mL 47593-0672-41 Ecolab 750 ml — — FDA listed —
Ecolab Foaming Antibacterial Handsoap 5 mg/mL 47593-0678-59 Ecolab 1250 ml — — FDA listed —
Rushing Foaming Antibacterial Handsoap 5 mg/mL 47593-0682-59 Ecolab 1250 ml — — FDA listed —
Kay RTU Foaming AB HandSoap 5 mg/mL 47593-0693-70 Ecolab 1200 ml — — FDA listed —
Fortress Foaming Antibacterial HandSoap 5 mg/mL 47593-0694-41 Ecolab 750 ml — — FDA listed —
CleanGenic Antibacterial Foam Hand 5 mg/.001L 60933-0050-00 Fuller 1 l — — FDA listed —
Simple Hygiene Antibacterial Foam Hand 5 mg/mL 60933-0106-01 Fuller 3790 ml — — FDA listed —
Sierra Soft Antibacterial Wash 5 g/L 70415-0001-01 CWGC 1 l — — FDA listed —
Sierrasoft Clear Antibacterial Wash Foam .5 g/100mL 70415-0901-01 CWGC 1000 ml — — FDA listed —
Hillyard Citrus Fresh Antimicrobial Foaming .5 g/100mL 76402-0408-02 Hillyard 1000 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

🏛️
2012
On the market since
Oct 2012
📍
2026
Currently FDA-listed
14 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
47593-0501-11 3780 mL in 1 BOTTLE, PLASTIC (47593-501-11) 2012-10-26 Active
47593-0501-26 1000 mL in 1 POUCH (47593-501-26) 2012-10-25 Discontinued by firm
47593-0501-31 540 mL in 1 BOTTLE, PLASTIC (47593-501-31) 2012-10-24 Active
47593-0501-32 1000 mL in 1 BOTTLE, PLASTIC (47593-501-32) 2012-10-24 Active
47593-0501-41 You're viewing this 750 mL in 1 BOTTLE, PLASTIC (47593-501-41) 2013-04-22 Active
47593-0501-56 1200 mL in 1 BOTTLE, PLASTIC (47593-501-56) 2012-10-26 Discontinued by firm
47593-0501-59 1250 mL in 1 BOTTLE, PLASTIC (47593-501-59) 2013-04-23 Active

Pack size FAQ

What quantity is in NDC 47593-0501-41?
NDC 47593-0501-41 contains 750 mL — 750 ml in 1 bottle, plastic.
What is the difference between NDC 47593-0501-41 and NDC 47593-0501-31?
Both are Ecolab Chloroxylenol 5.2 mg/mL Solution — the drug itself is identical. NDC 47593-0501-41 is the 750 mL package, while NDC 47593-0501-31 is the 540 ml package.
What NDC number is used to bill for this package of Ecolab Chloroxylenol 5.2 mg/mL Solution?
Bill NDC 47593-0501-41 — the 11-digit billing format is 47593050141. 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 47593-501-41, 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: 47593-0501-41, written without dashes as 47593050141. 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 47593-0501-41, the first segment (47593) is the labeler code FDA assigned to Ecolab Inc.; the middle segment (0501) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (41) 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 Ecolab 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 6 other package presentations of this same product, including 540 ml (47593-0501-31), 1000 ml (47593-0501-26), 1000 ml (47593-0501-32). 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?
Ecolab 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 13 words ▾

Uses For handwashing to decrease bacteria on the skin recommended for repeated use.

⏱️ Dosage and Administration 18 words ▾

Directions Wet skin and spread a small amount on hands and forearms Scrub well, rinse thoroughly and dry

⚠️ Warnings 66 words ▾

Warnings For external use only Do not use In eyes When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and redness develop Stop use and ask a doctor if skin irritation or redness occurs 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 4 words ▾

Active ingredient Chloroxylenol 0.5%

🧪 Inactive Ingredients 34 words ▾

Inactive ingredients water (aqua), potassium cocoate, hexylene glycol, sodium sulfate, tetrasodium EDTA, sodium lauryl sulfate, hydroxyethylcellulose, glycerin, cocoglucoside, glyceryl oleate, citric acid, frangrance, methylchloroisothiazolinone, methylisothiazolinone, FD&C red #40, FD&C yellow #5, D&C red #33

🎯 Purpose 3 words ▾

Purpose Antiseptic handwash

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 47593-0500-38 · Ecolab 47593-0502-31 · Ecolab →
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.