Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.
Ecolab Chloroxylenol 10 mg/mL Liquid, 750 mL — NDC 47593-506-41 (Billing 47593-0506-41)
by Ecolab Inc. · 750 mL in 1 BOTTLE, PLASTIC
This is a package of 750 mL of Ecolab Chloroxylenol 10 mg/mL Liquid from Ecolab Inc., marketed since Mar 2014 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.
NDC 47593-0506-41
🏷️ FDA NDC (as labeled)
47593-506-41
billing pads the product segment with a zero
This package
Contains750 mL
Pack sizes2 compare ↓
Main listing for product 47593-506 · Also comes in:
1250 ml 47593-506-59
🗂️ 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 →
NDC database record
One package, one record: these facts belong to NDC 47593-506-41 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 47593 labeler · 506 product · 41 package
- Package marketed since
- Mar 21, 2014
- Sample package
- No — commercial package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC)
- 0025469010957
- FDA record last changed
- Jul 24, 2026
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
FDA NDC (as labeled)
47593-506-41
Product NDC
47593-506
11-digit billing NDC
47593050641
RxCUI
413257
UNII
0F32U78V2Q
UPC
0025469010957
Application #
505G(a)(3)
SPL Set ID
174e2533-88a4-453d-ad5e-f936c4104c19
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2014-03-21
Route
TOPICAL
Dosage form
LIQUID
Substance
CHLOROXYLENOL
Quick answers
- RxCUI (RxNorm): 413257
Why two NDCs?
The FDA registers this code as 47593-506-41 — 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 → 47593-0506-41. 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 8, 2026
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.
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
🧪 What is this product?
Ecolab Chloroxylenol 10 mg/mL is a topical liquid containing chloroxylenol, an antimicrobial agent commonly used in cleansers and disinfectants. This product is marketed as an over-the-counter monograph drug, meaning it follows FDA's established rules for antiseptic and antimicrobial products rather than being individually reviewed. Chloroxylenol is typically included in products intended for skin cleansing and antimicrobial purposes.
Patient education
Supplement & herbal interactions
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.
- MedlinePlus (NLM) · refreshed Oct 8, 2026
- FDA label on DailyMed · label index refreshed Oct 8, 2026
💬 Questions about Chloroxylenol?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
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 system | Per mL | Per 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.
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 8, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 47593-0506-41 You're viewing this Main listing | 750 mL in 1 BOTTLE, PLASTIC | 2014-03-21 | — | Active |
| 47593-0506-59 47593-506-59 | 1250 mL in 1 BOTTLE, PLASTIC | 2014-03-21 | — | Active |
You're viewing the smallest of 2 pack sizes for this product.
Pack size FAQ
What quantity is in this package?
This package contains 750 mL — 750 ml in 1 bottle, plastic.
How does this package differ from NDC 47593-0506-59?
Both are Ecolab Chloroxylenol 10 mg/mL Liquid — the drug itself is identical. This page's package is the 750 mL one, while NDC 47593-0506-59 is the 1250 ml package.
What NDC number is used to bill for this package of Ecolab Chloroxylenol 10 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
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Kindest Kare Hand Antimicrobial Handwash 1 g/100mL 11084-0036-41 | SC | 1000 ml | — | — | FDA listed | — |
| Acute-Kare Healthcare Personnel Handwash 1 g/100mL 11084-0800-41 | SC | 1000 ml | — | — | FDA listed | — |
| DigiClean E 1 mg/100mL 47593-0308-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab 10 mg/mLthis 47593-0506-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| VioNexus 1 g/100mL 55443-0600-03 | Metrex | 2 bottles | — | — | FDA listed | — |
| SoftenSure Foam Antimicrobial 10 mg/mL 59900-0127-05 | Best | 1250 ml | — | — | FDA listed | — |
| Soften Sure Foam Antimicrobial 10 g/1000mL 59900-0211-06 | Best | 1000 ml | — | — | FDA listed | — |
| Prestige 10 mg/mL 63621-0335-14 | Sunburst | 3785 ml | — | — | FDA listed | — |
| FoamyIQ Healthcare Personnel Handwash 10.11 g/L 64009-0203-06 | Spartan | 1.25 l | — | — | FDA listed | — |
| Lite nFoamy Healthcare Personnel Handwash 10.11 g/L 64009-0335-82 | Spartan | 532 l | — | — | FDA listed | — |
| Antiseptic Hand Cleaner 10.11 g/L 64009-0336-85 | Spartan | 3.79 l | — | — | FDA listed | — |
| Clean Xpress Antiseptic Hand Cleaner 10 mg/mL 64009-0338-02 | Spartan | 1000 ml | — | — | FDA listed | — |
| Soft Care Defend Foam Antibacterial Handwash 1 g/100mL 64536-8308-02 | Diversey, | 1200 ml | — | — | Discontinued | — |
| Soft Care Defend Antibacterial Handwash 1 g/100mL 64536-8748-02 | Diversey, | 1200 ml | — | — | Discontinued | — |
| Soft Care Defend Antibacterial Handwash 10 g/L 64536-8760-02 | Diversey, | 3.78 l | — | — | FDA listed | — |
| WhiskCare 365 10 mg/mL 65585-0365-02 | Whisk | 3785 ml | — | — | FDA listed | — |
| AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL 66949-0139-01 | Zep | 208198 ml | — | — | FDA listed | — |
| AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL 66949-0141-01 | Zep | 208198 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.
- FDA openFDA NDC Directory · synced Oct 8, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
🏛️
2014
On the market since
Mar 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.
- FDA Orange Book · refreshed Oct 3, 2026
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 3K9958V90M
A liquid solvent derived from fermentation or chemical synthesis. In medicines, alcohol dissolves active ingredients, helps preserve the product, and improves how the body absorbs certain drugs.
-
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 QWA2IZI6FI
A surfactant derived from coconut oil, cocamine oxide helps reduce surface tension and improves how ingredients mix together in liquid formulations, enhancing product stability and texture.
-
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 H3R47K3TBD
FD&C Blue No. 1 is a synthetic blue dye approved for use in foods and medicines. It serves as a colorant to give the medication its distinctive appearance and help with product identification.
-
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 ND2M416302
Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
-
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 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII G4LZF950UR
Sodium xylenesulfonate is a synthetic organic salt used as a solubilizer and buffering agent in liquid medications. It helps dissolve active ingredients that don't mix well with water, improving how the medicine can be formulated and absorbed.
-
UNII 506T60A25R
Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in the product.
-
UNII 8W8T17847W
A nitrogen-containing chemical compound used in pharmaceuticals as a humectant to retain moisture, and sometimes as a keratolytic agent in topical formulations to help soften and remove dead skin cells.
-
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.
14 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesInactive ingredients water (aqua), propylene glycol, urea, sorbitol, potassium cocoate, tetrasodium EDTA, SD alcohol 3-C, glycerin, sodium xylenesulfonate, citric acid, fragrance, cocamine oxide, FDC yellow 5, FDC blue 1
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.- FDA label on DailyMed · label index refreshed Oct 8, 2026
- FDA openFDA NDC Directory · synced Oct 8, 2026
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
LabelerEcolab Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code47593
First marketedMar 2014
Product typeHuman Otc Drug
Portfolio115 products on file
More NDCs from Ecolab Inc. labeler code 47593
- PureForce Alcohol 534 mg/mL Solution NDC 47593-498-25
- Quik-Care Nourishing Foam Hand Sanitizer Alcohol 70 mL/100mL Solution NDC 47593-500-38
- Ecolab Chloroxylenol 5.2 mg/mL Solution NDC 47593-501-11
- Ecolab Alcohol 598.5 mg/mL Solution NDC 47593-502-31
- Ecolab Inc. Chloroxylenol 5 mg/mL Liquid NDC 47593-503-41
- Pure Force Benzalkonium chloride 1 mg/mL Liquid NDC 47593-504-41
- Ecolab Alcohol 60 mL/100mL Liquid NDC 47593-507-11
- Ecolab Facilipro Alcohol 60 mL/100mL Liquid NDC 47593-508-56
- Ecolab Alcohol 700 mg/mL Liquid NDC 47593-509-41
- Ecolab Inc. Benzalkonium chloride 8.9 mg/mL Solution NDC 47593-511-61
- Ecolab Inc. Benzalkonium chloride 8.9 mg/mL Solution NDC 47593-512-61
- Ecolab Inc. Benzalkonium chloride 8.9 mg/mL Solution NDC 47593-513-62
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 openFDA NDC Directory · synced Oct 8, 2026
- Drugs@FDA
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
📄 Do Not Use
📄 Ask a Doctor Before Use If
📄 When Using This Product
📄 Keep Out of Reach of Children
📄 Questions or Comments
📚 References
📄 Package Label / Principal Display Panel
🎯 Indications and Usage ▾
Uses For handwashing to decrease bacteria on the skin
⏱️ Dosage and Administration ▾
Directions Wet hands and apply foam Scrub hands and forearm Rinse thoroughly and dry
⚠️ Warnings ▾
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 for 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active ingredient Chloroxylenol 1.0%
🧪 Inactive Ingredients ▾
Inactive ingredients water (aqua), propylene glycol, urea, sorbitol, potassium cocoate, tetrasodium EDTA, SD alcohol 3-C, glycerin, sodium xylenesulfonate, citric acid, fragrance, cocamine oxide, FDC yellow 5, FDC blue 1
🎯 Purpose ▾
Purpose Antiseptic handwash
📄 Do Not Use ▾
Do not use In eyes
📄 Ask a Doctor Before Use If ▾
Stop use and ask a doctor if Skin irritation or redness occurs for more for 72 hours
📄 When Using This Product ▾
When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and redness develop
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Questions or Comments ▾
Questions? call 1.800.35.CLEAN (352.5326)
📚 References ▾
Other information For additional information, see Safety Data Sheet (SDS) EMERGENCY HEALTH INFORMATION: 1 800 328 0026. If located outside the United States and Canada, call collect 1 651 222 5352 (number is in the US).
📄 Package Label / Principal Display Panel ▾
Principal Display Panel and Representative Label ECOLAB ® 6100719 Gentle Antibacterial Foam Hand Soap 750 ML (25 US FL OZ) Active ingredient: Chloroxylenol 1.0% 755511/5403/0321 Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA tel: 1 800 35 CLEAN (352 5326) © 2021 Ecolab USA Inc. · All rights reserved Made in U.S.A. representative label
No label section mentions that — try another word, or open the full label on DailyMed below.
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 Ecolab (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 54%
Female · 46%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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
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 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 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 1 other package presentation of this same product, including 1250 ml (47593-0506-59). 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.
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.