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Facilipro Ethyl Alcohol 620 mg/mL Solution, 1200 mL — NDC 47593-0563-56 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Facilipro Ethyl Alcohol 620 mg/mL Solution, 1200 mL — NDC 47593-563-56 (Billing 47593-0563-56)

by Ecolab Inc. · 1200 mL in 1 BOTTLE, PLASTIC

This is a package of 1,200 mL of Facilipro Ethyl Alcohol 620 mg/mL Solution from Ecolab Inc., marketed since Dec 2010 and currently FDA-listed. It is this product's only package size.

NDC 47593-0563-56
🏷️ FDA NDC (as labeled) 47593-563-56 billing pads the product segment with a zero
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

⚠️
Other active recalls for Ethyl Alcohol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 23, 2025 — Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol (Consumer Product Partners, LLC) · FDA recall D-0458-2025
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) 47593-563-56
Product NDC 47593-563
11-digit billing NDC 47593056356
RxCUI 247835
UNII 3K9958V90M
UPC 0025469012586
Application # 505G(a)(3)
SPL Set ID 71f2504a-2da3-4273-9603-47e4cf64ad24
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2010-12-03
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 247835
Why two NDCs? The FDA registers this code as 47593-563-56 — 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 → 47593-0563-56. 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.
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
47593-0563-56 You're viewing this Main listing 1200 mL in 1 BOTTLE, PLASTIC 2010-12-03 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Alcohol 62 mL/100mL 00363-0046-16 Walgreen 59 ml — — FDA listed —
Alcohol 62 mL/100mL 11344-0849-16 Nice-Pak 59 ml — — FDA listed —
Alcohol 62 mL/100mL 11673-0826-16 Target 59 ml — — FDA listed —
Alcohol 62 mL/100mL 30142-0849-16 The 59 ml — — FDA listed —
Symmetry Hand Sanitizer 62 mL/100mL 30805-0001-01 Buckeye 9 ml — — FDA listed —
Altra Hand Sanitizer with Aloe and Vitamin E 62 mL/100mL 30805-0014-06 Buckeye 59.2 ml — — FDA listed —
Alcohol 62 mL/100mL 41163-0826-16 United 59 ml — — FDA listed —
Alcohol 62 mL/100mL 41163-0975-16 United 59 ml — — FDA listed —
Alcohol 62 mg/mL 41190-0849-16 Wakefern 59 ml — — FDA listed —
Ecolab 620 mg/mL 47593-0489-33 Ecolab 118 ml — — FDA listed —
Facilipro 620 mg/mLthis 47593-0563-56 Ecolab 1200 ml — — FDA listed —
Safety 1st Oh Sh t Kit 50428-0033-01 Dorel 1 kit — — FDA listed —
Alcohol 62 mL/100mL 55910-0889-48 Old 1005 ml — — Discontinued —
XtraCare Instant Hand Sanitizer 37 g/60g 57337-0058-02 Rejoice 60 g — — FDA listed —
XtraCare Instant Hand Sanitizer 37 g/60g 57337-0059-02 Rejoice 60 g — — FDA listed —
Alcohol 62 mL/100mL 59450-0471-16 The 89 ml — — Discontinued —
Lacura Moisturizing Hand Sanitizer 62 g/100mL 64024-0008-08 Aldi 236 ml — — FDA listed —
Antibacterial Hand Sanitizer 62 mL/100mL 71160-0188-12 TEKWELD 12 ml — — FDA listed —
Freeman Packaging Hand Sanitizer 62 mL/100mL 71734-0201-01 JIANGMEN 7.5 ml — — FDA listed —
KidzStuff Hand Sanitizer 62 g/100g 71734-0204-01 JIANGMEN 2 g — — FDA listed —
Afassco Hand Sanitizer 62 mL/100mL 71734-0206-01 JIANGMEN 2 ml — — FDA listed —
Hand Sanitizer 62 g/100g 71734-0348-01 JIANGMEN 4.2 g — — FDA listed —
Mrs. Meyers Clean Day Hand Sanitizer Basil Scent .62 mL/mL 71763-0101-01 The 59 ml — — FDA listed —
Mrs. Meyers Clean Day Hand Sanitizer Lavender Scent .62 mL/mL 71763-0201-01 The 59 ml — — FDA listed —
Alcohol 62 mL/100mL 72288-0826-32 Amazon.com 354 ml — — FDA listed —
Alcohol 62 mL/100mL 72288-0849-32 Amazon.com 354 ml — — FDA listed —
Hand Sanitizer Fresh Linen 62 mL/100mL 73928-0065-02 Kingkey 35 ml — — FDA listed —
Hand Sanitizer Strawberry Fizz 62 mL/100mL 73928-0066-02 Kingkey 35 ml — — FDA listed —
Hand Sanitizer Pink Sugar 62 mL/100mL 73928-0067-01 Kingkey 30 ml — — FDA listed —
Hand Sanitizer Vanilla 62 mL/100mL 73928-0068-02 Kingkey 35 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 73928-0079-02 Kingkey 35 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 73928-0081-01 Kingkey 35 ml — — FDA listed —
Jolly Rancher Hand Sanitizer Set Cherry 62 mL/100mL 73928-0112-01 Kingkey 35 ml — — FDA listed —
Smarties Orange Hand Santizer Set Orange Creamsicle 62 mL/100mL 73928-0113-01 Kingkey 35 ml — — FDA listed —
Sourpatch Kids Hand Sanitizer Set Watermelon 62 mL/100mL 73928-0114-01 Kingkey 35 ml — — FDA listed —
Jolly Rancher Hand Sanitizer Blue Raspberry 62 mL/100mL 73928-0115-01 Kingkey 35 ml — — FDA listed —
Jolly Rancher Hand Sanitizer Cherry 62 mL/100mL 73928-0117-01 Kingkey 35 ml — — FDA listed —
Smarties Hand Sanitizer Orange Creamsicle 62 mL/100mL 73928-0118-01 Kingkey 35 ml — — FDA listed —
Smarties Orange Hand Sanitizer Raspberry Cream 62 mL/100mL 73928-0119-01 Kingkey 35 ml — — FDA listed —
Smarties Orange Hand Sanitizer Mix Berry 62 mL/100mL 73928-0121-01 Kingkey 35 ml — — FDA listed —
Sourpatch Kids Hand Sanitizer Strawberry 62 mL/100mL 73928-0122-01 Kingkey 35 ml — — FDA listed —
Sour Patch Kids Hand Sanitizer Blue Raspberry 62 mL/100mL 73928-0123-01 Kingkey 35 ml — — FDA listed —
Sour Patch Kids Hand Sanitizer Watermelon 62 mL/100mL 73928-0124-01 Kingkey 35 ml — — FDA listed —
Dasiy Hand Sanitizer 62 mL/100mL 73928-0125-01 Kingkey 35 ml — — FDA listed —
Dasiy Hand Sanitizer 62 mL/100mL 73928-0126-01 Kingkey 35 ml — — FDA listed —
Kool Aid Ppink Lemonade Hydrating Hand Sanitizer 62 mL/100mL 73928-0187-01 Kingkey 35 ml — — FDA listed —
Pesi Vanilla Hydratiing Hand Sanitizer 62 mL/100mL 73928-0188-01 Kingkey 35 ml — — FDA listed —
Icee Cherry Hydrating Hand Sanitizer 62 mL/100mL 73928-0189-01 Kingkey 35 ml — — FDA listed —
Jolly Rancher Blue Raspberry Hydrating Hand Sanitizer 62 mL/100mL 73928-0191-01 Kingkey 35 ml — — FDA listed —
Mountain Dew Hydrating Hand Sanitizer 62 mL/100mL 73928-0210-01 Kingkey 35 ml — — FDA listed —
Liquid death hand sanitizer 62 mL/100mL 73928-0211-01 Kingkey 35 ml — — FDA listed —
Dubble Bubble Original Flavor Bubble Gum Hydrating Hand Sanitizer 62 mL/100mL 73928-0217-01 Kingkey 35 ml — — FDA listed —
Sourpatchkids Strawberry Hydrating Hand Sanitizer 62 mL/100mL 73928-0311-01 Kingkey 35 ml — — FDA listed —
Ethyl Alcohol 62 mL/100mL 75712-0849-16 Old 59 ml — — FDA listed —
Alcohol 62 mL/100mL 79481-0826-01 Meijer, 59 ml — — FDA listed —
Alcohol 62 mL/100mL 79481-0849-01 Meijer, 59 ml — — FDA listed —
Antibacterial Hand Sanitizer 62 mL/100mL 82953-0001-01 Cosmuses 10 ml — — FDA listed —
antiseptic hand sanitizer 01 62 mL/100mL 82953-0007-01 Cosmuses 10 ml — — FDA listed —
Antibacterial Hand Sanitizer 62 mL/100mL 82953-0008-01 Cosmuses 15 ml — — FDA listed —
hand sanitizer 01 62 mL/100mL 82953-0015-01 Cosmuses 10 ml — — FDA listed —
Antiseptic Hand Sanitizer 620 mg/g 82996-0005-01 Hubei 9 g — — FDA listed —
Antiseptic Hand Sanitizer 62 mL/100mL 83165-0000-00 Hubei 1.03 ml — — FDA listed —
Ethyl Alcohol 62 mL/100mL 83986-0471-16 UpLift 59 ml — — FDA listed —
Ethyl Alcohol 62 mL/100mL 83986-0973-16 UpLift 59 ml — — FDA listed —
Antiseptic Hand Sanitizer Ethyl Alcohol 62 g/100g 84219-0005-00 M-star 9 g — — FDA listed —
Huanggang Antiseptic Hand Sanitizer 62 mL/100mL 85426-0001-01 Huanggang 9 ml — — Discontinued —
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

🏛️
2010
On the market since
Dec 2010
📍
2026
Currently FDA-listed
16 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.

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

  • UNII 36HQN158VC
    Alpha-bisabolol is a naturally derived oily liquid from plant sources. It works as a fragrance, flavor, and skin-conditioning agent in topical medicines and cosmetic products.
  • UNII 2CNS542YRT
    A silicone-based compound that acts as an emulsifier and surfactant to help blend oil and water ingredients together. It improves the texture and spreadability of topical products like creams and lotions.
  • UNII 4YK5Z54AT2
    Denatonium benzoate is a bitter-tasting chemical compound added to medicines to discourage accidental ingestion, especially by children. It serves as a bittering agent with no therapeutic effect on the body.
  • UNII 147D247K3P
    Ethylhexylglycerin is a synthetic preservative used to prevent bacteria and mold from growing in medicines and personal care products. It helps keep the product safe and stable throughout its shelf life.
  • UNII EB41QIU6JL
    Farnesol is a natural fragrant compound found in plants. It's used in medicines as a preservative and flavoring agent to improve taste and help prevent microbial growth.
  • UNII MD83SFE959
    A volatile organic liquid used as a solvent and preservative in medications. It helps dissolve active ingredients and other components, and can improve product stability and shelf life.
  • 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.

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

The official label also statesInactive ingredeints   water (aqua), PEG-10 dimethicone, ethylhexylglycerin, farnesol, bisabolol, tert-butyl alcohol, dentonium benzoate

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 marketedDec 2010
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.

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📚 References 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses For hand washing to decrease bacteria on the skin

⏱️ Dosage and Administration 23 words ▾

Directions wash hands to remove soil dispense palmful spread to cover hands, rub in well air dry, do not rinse or towel dry

⚠️ Warnings 80 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 redness develop Stop use and ask a doctor if skin irritation and redness persist 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 Ethyl alcohol, 62% w/w

🧪 Inactive Ingredients 13 words ▾

Inactive ingredeints water (aqua), PEG-10 dimethicone, ethylhexylglycerin, farnesol, bisabolol, tert-butyl alcohol, dentonium benzoate

🎯 Purpose 3 words ▾

Purpose Antiseptic handwash

📄 Do Not Use 5 words ▾

Do not use in eyes

📄 When Using This Product 20 words ▾

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 17 words ▾

Stop use and ask a doctor if skin irritation and redness persist for more than 72 hours

📄 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 37 words ▾

Other information for additional information, see Material Safety Data Sheet (MSDS) 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 79 words ▾

Principal Display Panel and Representative label ECOLAB ® 6100781 FACILIPRO ™ Waterless Foam Hand Sanitizer Sanitizante en espuma sin agua para manos 1200 mL (40.6 US FL OZ) Active Ingredient: Ethyl alcohol 62% w/w Ecolab · 1 Ecolab Place · St. Paul MN 55102 USA · tel: 1 800 35 CLEAN (352 5326) © 2020 Ecolab USA Inc. · All rights reserved | Todos los derechos reservados Made in U.S.A. | Hecho en EE.UU. www.ecolab.com SDS-WI-15014, SDS-NJ-20007 representative label

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) ✓ 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.
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.
← 47593-0561-41 · Ecolab 47593-0565-59 · 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.