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Ecolab Ethyl Alcohol 620 mg/mL Solution, 37 mL — NDC 47593-0489-49 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Ecolab Ethyl Alcohol 620 mg/mL Solution, 37 mL — NDC 47593-489-49 (Billing 47593-0489-49)

by Ecolab Inc. · 37 mL in 1 BOTTLE, PLASTIC

This is a package of 37 mL of Ecolab Ethyl Alcohol 620 mg/mL Solution from Ecolab Inc., marketed since Dec 2013 and currently FDA-listed.

NDC 47593-0489-49
🏷️ FDA NDC (as labeled) 47593-489-49 billing pads the product segment with a zero
This package
Contains37 mL Pack sizes3 compare ↓
Product page 47593-0489-33 Also comes in: 118 ml 47593-489-33 1000 ml 47593-489-55
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) 47593-489-49
Product NDC 47593-489
11-digit billing NDC 47593048949
RxCUI 247835
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID f30e801c-d7ae-4a6f-830b-31d86c4f5b8c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-12-07
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 247835
Why two NDCs? The FDA registers this code as 47593-489-49 — 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 → 47593-0489-49. 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: 118 ml 1000 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
47593-0489-33 47593-489-33 Main listing 118 mL in 1 BOTTLE, PLASTIC 2013-12-07 — Active
47593-0489-49 You're viewing this 37 mL in 1 BOTTLE, PLASTIC 2013-12-07 — Active
47593-0489-55 47593-489-55 1000 mL in 1 BOTTLE, PLASTIC 2013-12-07 — Active

You're viewing the smallest of 3 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 37 mL — 37 ml in 1 bottle, plastic.
How does this package differ from NDC 47593-0489-33?
Both are Ecolab Ethyl Alcohol 620 mg/mL Solution — the drug itself is identical. This page's package is the 37 mL one, while NDC 47593-0489-33 is the 118 ml package.
What NDC number is used to bill for this package of Ecolab Ethyl Alcohol 620 mg/mL Solution?
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
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/mLthis 47593-0489-49 Ecolab 37 ml — — FDA listed —
Facilipro 620 mg/mL 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

🏛️
2013
On the market since
Dec 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.

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

  • UNII 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • UNII A9EJ3J61HQ
    A synthetic liquid derived from benzoic acid and long-chain alcohols. It functions as a solvent and penetration enhancer in topical formulations, helping active ingredients dissolve and absorb into the skin.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 59TL3WG5CO
    A synthetic polymer made by crosslinking acrylic acid with allyl sucrose. It thickens liquids, forms gels, and helps control how fast the medicine is released in your body.
  • 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 92RU3N3Y1O
    Dimethicone is a silicone-based oil that acts as an anti-foaming agent and lubricant in medicines. It reduces gas bubbles in liquid formulations and helps coat and protect the stomach lining when ingested.
  • UNII K5APE098ZI
    A synthetic chemical compound used as a chelating agent and stabilizer in medicines. It helps bind to metal ions and prevent unwanted chemical reactions that could degrade the drug's quality during storage.
  • 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 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 8CRQ2TH63M
    Isopropyl palmitate is an oily liquid derived from palm oil. It acts as an emollient and lubricant in medicines, helping soften the skin or improve how the product spreads and flows.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • 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.

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

The official label also statesInactive ingredients water (aqua), glycerin, tetrahydroxyethyl ethylenediamine, ethylhexylglycerin, isopropyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, C12-C15 alkyl benzoate, panthenol, tert-butyl alcohol, tocopheryl acetate, dimethicone, aloe barbadensis leaf juice, denatonium 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 2013
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 📄 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 10 words ▾

Directions Apply product onto hands, spread thoroughly and rub dry

⚠️ Warnings 79 words ▾

Warnings For external use only Flammable, keep away from fire or flame, heat, sparts 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 doctor if Skin irritation or redness persists 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 29 words ▾

Inactive ingredients water (aqua), glycerin, tetrahydroxyethyl ethylenediamine, ethylhexylglycerin, isopropyl palmitate, acrylates/C10-30 alkyl acrylate crosspolymer, C12-C15 alkyl benzoate, panthenol, tert-butyl alcohol, tocopheryl acetate, dimethicone, aloe barbadensis leaf juice, denatonium benzoate

🎯 Purpose 3 words ▾

Purpose Antiseptic handwash

📄 Do Not Use 5 words ▾

Do not use In eyes

📄 Ask a Doctor Before Use If 16 words ▾

Stop use and ask doctor if Skin irritation or redness persists 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 redness 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 6 words ▾

Questions? call 1 866 781 8787

📚 References 24 words ▾

Other information for additional information, see Material Safety Data Sheet (MSDS) for emergency medical information in USA and Canada, call 1 800 328 0026

📄 Package Label / Principal Display Panel 60 words ▾

Representative Label and Principal Display Panel ECOLAB ® NDC 47593-489-55 Moisturizing Gel Hand Sanitizer Dye and Fragrance Free Active Ingredient: 62% Ethyl Alcohol Net Contents: 6084642 1000 mL (33.8 fl oz) 746338/8501/0912 Ecolab · 370 Wabasha Street N · St Paul MN 55102-1390 USA © 2018 Ecolab USA Inc · All rights reserved Made in United States 746340/8502/1218 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 2 other package presentations of this same product, including 118 ml (47593-0489-33), 1000 ml (47593-0489-55). 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.
← 47593-0488-26 · Ecolab 47593-0490-82 · 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.