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Ecolab Alcohol 60 mL/100mL Liquid, 750 mL — NDC 47593-0507-41 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ecolab Alcohol 60 mL/100mL Liquid, 750 mL — NDC 47593-507-41 (Billing 47593-0507-41)

by Ecolab Inc. · 750 mL in 1 BOTTLE, PLASTIC

This is a package of 750 mL of Ecolab Alcohol 60 mL/100mL Liquid from Ecolab Inc., marketed since Oct 2013 and currently FDA-listed.

NDC 47593-0507-41
🏷️ FDA NDC (as labeled) 47593-507-41 billing pads the product segment with a zero
This package
Contains750 mL Pack sizes4 compare ↓
Product page 47593-0507-11 Also comes in: 1200 ml 47593-507-56 1200 ml 47593-507-70 3780 ml 47593-507-11
OTC On market Non-controlled ⇄ 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 47593-507-41 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
47593 labeler · 507 product · 41 package
Package marketed since
Oct 31, 2013
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC)
0025469082930
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 47593-507-41
Product NDC 47593-507
11-digit billing NDC 47593050741
RxCUI 581658
UNII 3K9958V90M
UPC 0025469082930
Application # 505G(a)(3)
SPL Set ID f8561810-9d12-4c05-a547-b41bbb5170a9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-10-31
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 581658
Why two NDCs? The FDA registers this code as 47593-507-41 — 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 → 47593-0507-41. 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 Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants
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

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 Read our full Alcohol guide →

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: 1200 ml 1200 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.

Packaging — all sizes for this product

Package NDCDescription Marketing startMarketing endStatus
47593-0507-41 You're viewing this 750 mL in 1 BOTTLE, PLASTIC 2013-10-31 — Active
47593-0507-56 47593-507-56 1200 mL in 1 BOTTLE, PLASTIC 2013-10-31 — Active
47593-0507-11 47593-507-11 Main listing 3780 mL in 1 BOTTLE, PLASTIC 2023-01-31 — Active
47593-0507-70 47593-507-70 1200 mL in 1 BOTTLE, PLASTIC 2025-05-22 — Active

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 47593-0507-56?
Both are Ecolab Alcohol 60 mL/100mL Liquid — the drug itself is identical. This page's package is the 750 mL one, while NDC 47593-0507-56 is the 1200 ml package.
What NDC number is used to bill for this package of Ecolab Alcohol 60 mL/100mL 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
Isagel 600 mL/1000mL 11701-0025-45 Coloplast 800 ml — — Discontinued —
Ecolab 60 mL/100mLthis 47593-0507-41 Ecolab 750 ml — — FDA listed —
Ecolab Facilipro 60 mL/100mL 47593-0508-56 Ecolab 1200 ml — — FDA listed —
Ecolab Clear 60 mL/100mL 47593-0638-41 Ecolab 750 ml — — Discontinued —
SSDC Gel Hand Sanitizer 60 mL/100mL 47593-0664-70 Ecolab 1200 ml — — FDA listed —
Covex Antibacterial Hand Sanitizer, COOL BREEZE .6 mL/mL 51209-0012-00 DALAN 236 ml — — FDA listed —
Covex Antibacterial Hand Sanitizer, FRESH ALOE .6 mL/mL 51209-0013-00 DALAN 236 ml — — FDA listed —
Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer 600 mL/L 51801-0437-08 Nomax, 237 l — — FDA listed —
SunDrops 75 .6 mL/mL 63621-0356-14 Sunburst 3785 ml — — FDA listed —
Aire-Master Hand Sanitizer 600 mL/L 65585-0358-01 Whisk 473 l — — FDA listed —
Sani-Sure 600 mL/L 65585-0359-01 Whisk 237 l — — FDA listed —
WhiskCare 375 600 mL/L 65585-0375-01 Whisk 8 l — — Discontinued —
WhiskCare 375 Fragrance Free 600 mL/L 65585-0378-01 Whisk 8 l — — FDA listed —
Pacific Breeze Instant Hand Sanitizer Gel 600 mL/L 65585-0380-01 Whisk 1 l — — FDA listed —
D-Germ 600 mL/L 65585-0498-01 Whisk 118 l — — FDA listed —
Algonquin HanSan 600 mL/L 65585-0522-02 Whisk 237 l — — FDA listed —
Aire-Master Waterless Hand Sanitizer 600 mL/L 65585-0525-01 Whisk 8 l — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2074-01 Raining 44 ml — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2075-01 Raining 30 ml — — FDA listed —
Unscented Hand Sanitizer 60 mL/100mL 65692-2076-01 Raining 59 ml — — FDA listed —
Vindicator Instant Hand Sanitizer 600 mL/1000mL 66608-0515-05 Kimball 3785 ml — — Discontinued —
Natural Extensions Fragrance- Free Instant Hand Sanitizer 60 mL/100mL 66975-0101-02 Benco 251 ml — — FDA listed —
Applause 3 g/5g 67858-0693-02 QuestSpecialty 24 bottles — — FDA listed —
Avant Original - Fragrance Free 60 mL/100mL 68306-0106-01 B4 82.5 ml — — Discontinued —
Zogics Instant Hand Sanitizer Hydrating Gel 60 mL/100mL 72202-0026-01 Zogics, 1000 ml — — FDA listed —
palm party 60 mL/100mL 87322-1614-01 Dongyang 30 ml — — FDA listed —
Clean and Go 600 mL/1000mL 87377-0001-01 Satellite 800 ml — — Discontinued —
Retail Hand Sanitizer 60 mL/100mL 47593-0684-56 Ecolab 1200 ml — — FDA listed —
Alcohol Gel Hand Sanitizer 60 mL/100mL 47593-0690-70 Ecolab 1200 ml — — FDA listed —
Pureforce 60 mL/100mL 47593-0473-25 Ecolab 800 ml — — Discontinued —
Chemstar Retail Hand Sanitizer 60 mL/100mL 47593-0687-56 Ecolab 1200 ml — — FDA listed —
Keystone Liquid Hand Sanitizer 60 mL/100mL 47593-0466-25 Ecolab 800 ml — — FDA listed —
First Mark Ultra Hand Sanitizer 60 mL/100mL 51042-0002-09 Performance 1200 ml — — FDA listed —
Sysco Reliance 60 mL/100mL 47593-0480-25 Ecolab 800 ml — — Discontinued —
SSDC Alphasan Hand Sanitizer 60 mL/100mL 47593-0680-25 Ecolab 800 ml — — FDA listed —
QSR Hand Sanitizer 60 mL/100mL 47593-0673-25 Ecolab 800 ml — — FDA listed —
Swisher Instant Hand Sanitizer Gel 60 mL/100mL 47593-0697-41 Ecolab 750 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

🏛️
2013
On the market since
Oct 2013
📍
2026
Currently FDA-listed
13 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII 809Y72KV36
    A synthetic polymer made from acrylic acid and crosslinked with allyl pentaerythritol. It's used as a thickening agent and gelling ingredient in creams, gels, and lotions to create the proper texture and help the medicine spread and stay on the skin.
  • 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 V42034O9PU
    A fatty alcohol derived from coconut or palm oil. It serves as an emulsifier and thickener to help blend oil and water in creams or lotions, and improves the product's texture and consistency.
  • 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 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • 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.

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

The official label also statesInactive ingredients  water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

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.

Manufacturer & labeler

LabelerEcolab Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code47593
First marketedOct 2013
Product typeHuman Otc Drug
Portfolio115 products on file

More NDCs from Ecolab Inc. labeler code 47593

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 📄 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 9 words ▾

Uses For handwashing to decrease bacteria on the skin

⏱️ Dosage and Administration 23 words ▾

Directions Apply liberal amount into hand Spread by rubbing hands together Rub to dryness with attention to are around nails and between fingers

⚠️ Warnings 82 words ▾

Warnings For external use only FLAMMABLE, keep away from fire or flame, heat, sparks and sources of static discharge Do not use In eyes When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and rendess develop Stop use and ask a doctor if eye or skin irritation or redenss 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 6 words ▾

Active ingredient Ethanol 60% by volume

🧪 Inactive Ingredients 15 words ▾

Inactive ingredients water (aqua), isopropyl alcohol, triethanolamine, acrylates/C10-30 alkyl acrylate crosspolymer, propylene glycol, myristyl alcohol

🎯 Purpose 3 words ▾

Purpose Antispetic handwash

📄 Do Not Use 5 words ▾

Do not use In eyes

📄 Ask a Doctor Before Use If 19 words ▾

Stop use and ask a doctor if eye or skin irritation or redenss occurs for more than 72 hours

📄 When Using This Product 20 words ▾

When using this product If in eyes, rinse promptly and thoroughly with water Discontinue use if irritation and rendess develop

📄 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.

📄 Questions or Comments 4 words ▾

Questions? call 1-800-35-CLEAN (352-5326)

📚 References 36 words ▾

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 60 words ▾

Principal Display Panel and Representative Label ECOLAB ® 6102487 Instant Hand Sanitizer Gel

3.78L (1 US GAL) Active Ingredient: Ethanol 60% by volume Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326) © 2023 Ecolab USA Inc. · All rights reserved Made in U.S.A. www.ecolab.com · 780002/5400/0123 representative 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 Ecolab (this brand).

Top reported reactions

Toxicity To Various Agents6,041
Completed Suicide5,451
Drug Abuse5,333
Overdose1,922
Death1,631
Intentional Overdose1,559
Suicide Attempt1,360

Age at onset

Neonate26
Infant15
Child16
Adolescent97
Adult2,909
Elderly315

Reporter sex

27,829 reports
Male · 54%
Female · 46%
Unknown · 0%

Serious outcomes

Death15,642
Hospitalization9,024
Life-threatening1,546
Disabling329
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,724 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
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 3 other package presentations of this same product, including 1200 ml (47593-0507-56), 1200 ml (47593-0507-70), 3780 ml (47593-0507-11). 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.
← 47593-0506-41 · Ecolab 47593-0508-56 · 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.