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eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL Solution, 1200 mL — NDC 50865-0688-50 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL Solution, 1200 mL — NDC 50865-688-50 (Billing 50865-0688-50)

by Kutol Products Company · 1200 mL in 1 BAG

This is a package of 1,200 mL of eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL Solution from Kutol Products Company, marketed since Jun 2013 and currently FDA-listed.

NDC 50865-0688-50
🏷️ FDA NDC (as labeled) 50865-688-50 billing pads the product segment with a zero
This package
Contains1200 mL Pack sizes6 compare ↓
Product page 50865-0688-09 Also comes in: 50 ml 50865-688-17 950 ml 50865-688-78 1000 ml 50865-688-24 1000 ml 50865-688-41 3785 ml 50865-688-09
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 50865-688-50
Product NDC 50865-688
11-digit billing NDC 50865068850
RxCUI 616763
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 1f56b4c5-d703-4193-83a8-3be815c8acda
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2013-06-27
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616763
Why two NDCs? The FDA registers this code as 50865-688-50 — 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 → 50865-0688-50. 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: 50 ml 950 ml 1000 ml 1000 ml 3785 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
50865-0688-09 50865-688-09 Main listing 3785 mL in 1 JUG 2013-06-27 — Active
50865-0688-17 50865-688-17 50 mL in 1 BOTTLE, PLASTIC 2013-06-27 — Active
50865-0688-24 50865-688-24 1000 mL in 1 BAG 2013-06-27 — Active
50865-0688-41 50865-688-41 1000 mL in 1 BAG 2013-06-27 — Active
50865-0688-50 You're viewing this 1200 mL in 1 BAG 2013-06-27 — Active
50865-0688-78 50865-688-78 950 mL in 1 BOTTLE, PLASTIC 2013-06-27 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1200 mL — 1200 ml in 1 bag.
How does this package differ from NDC 50865-0688-17?
Both are eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL Solution — the drug itself is identical. This page's package is the 1200 mL one, while NDC 50865-0688-17 is the 50 ml package.
What NDC number is used to bill for this package of eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mL 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
Alcare OR Foamed Antiseptic Handrub 62 g/100g 11084-0802-80 SC 482 g — — FDA listed —
Alcare Plus Foamed Antiseptic Handrub 62 g/100g 11084-0803-36 SC 255 g — — FDA listed —
FoamFresh Alco-Foam Hand Sanitizer 62 mL/100mL 11429-1004-00 Woodbine 400 ml — — FDA listed —
Doctors Kline and Green Board Certified Dermatologist Hand Sanitizer Antiseptic 62 mL/100mL 23667-0104-00 Formulated 222 ml — — Discontinued —
Symmetry Foaming Hand Sanitizer 62 mL/100mL 30805-0003-03 Buckeye 2000 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer-Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0009-04 Buckeye 1200 ml — — FDA listed —
Altra Foaming Hand Sanitizer with Aloe and Vitamin E 62 mL/100mL 30805-0012-04 Buckeye 1200 ml — — FDA listed —
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 62 mL/100mL 30805-0013-04 Buckeye 1200 ml — — FDA listed —
Hand Guard Foaming Alcohol Instant Hand Sanitizer 620 mL/L 31507-0024-24 Wechem, 1 l — — FDA listed —
Hand Guard Foaming Instant Hand Sanitizer .62 mL/mL 31507-0585-08 Wechem, 1000 ml — — FDA listed —
Ecolab 62 mL/100mL 47593-0472-41 Ecolab 750 ml — — FDA listed —
eZFoam Foaming Alcohol Hand Sanitizer 62 mL/100mLthis 50865-0688-50 Kutol 1200 ml — — FDA listed —
Amcon Labs Hand Sanitizer Instant Foam Sanitizer with Alcohol 620 mL/L 51801-0366-18 Nomax, 55 l — — FDA listed —
Scott Moisturizing Foam Hand Sanitizer 62 mL/100mL 55118-0546-63 Kimberly-Clark 6 bottles — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Cherry Scented 62 mL/100mL 56136-0021-01 Ganzhou 50 ml — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Pineapple Scented 62 mL/100mL 56136-0022-01 Ganzhou 50 ml — — FDA listed —
Foaming Mousse Anti-Bacterial Hand Sanitizer Pink Grapefruit Scented 62 mL/100mL 56136-0023-01 Ganzhou 50 ml — — FDA listed —
Alpet E3 Hand Sanitizer Foam 62 mL/100mL 59900-0125-02 Best 208197 ml — — FDA listed —
Simple Hygiene foaming hand Sanitizer 62 .62 mL/mL 60933-0062-01 FULLER 1000 ml — — FDA listed —
Simple Hygiene Hand Sanitizer 620 mg/mL 60933-0220-00 FULLER 1000 ml — — FDA listed —
Foaming Alcohol Hand Sanitizer .62 mL/mL 63900-0002-00 Simoniz 1000 ml — — FDA listed —
Soft Care Foam Instant Hand Sanitizer 62 mL/100mL 64536-7295-04 Diversey, 532 ml — — FDA listed —
WhiskCare 373 620 mL/L 65585-0374-01 Whisk 1 l — — Discontinued —
Aire-Master Foaming Hand Sanitizer Fragrance Free 620 mL/L 65585-0524-01 Whisk 3.785 l — — FDA listed —
Avant Foaming Hand Sanitizer 62 mL/100mL 68306-0109-01 B4 530 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 69674-0100-01 Saraya 500 ml — — FDA listed —
Servo Stat-Foam 62 mL/100mL 76378-0011-01 Enzyme 59 ml — — FDA listed —
Hillyard Foaming Instant Hand Sanitizer 62 mL/100mL 76402-0410-02 Hillyard 1000 ml — — FDA listed —
CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0000-01 CleanGenic, 3790 ml — — FDA listed —
CleanGenic 1 GALLON HAND SANITIZER 62 mL/100mL 81385-0001-04 CleanGenic, 24 bottles — — FDA listed —
CleanGenic Foaming Hand Sanitizer 62 mL/100mL 81385-0002-08 CleanGenic, 237 ml — — FDA listed —
CleanGenic 8 OZ HAND SANITIZER 62 mL/100mL 81385-0003-08 CleanGenic, 24 bottles — — FDA listed —
Transcend Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0001-01 Von 1250 ml — — FDA listed —
Harbor Mist Alco-Foam Hand Sanitizer 62 mL/100mL 81792-0003-01 Von 1250 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
Jun 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 QCD5R22RNT
    A fluorinated phosphate compound used as a surfactant and emulsifier in topical formulations. It helps mix oil and water-based ingredients together and improves product texture and spreadability on skin.
  • 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 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.

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

The official label also statesWater, AMP-C8-18 Perfluoroalkylethyl Phosphate, Glycerin.

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

LabelerKutol Products Company
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code50865
First marketedJun 2013
Product typeHuman Otc Drug
Portfolio7 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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 64 words ▾

Hand sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use. Avoid contact with eyes. If eye contact occurs, flush with water. Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, contact a physician or poison control center.

⏱️ Dosage and Administration 18 words ▾

To decrease bacteria on skin, apply small amount to palm. Briskly rub, covering hands with product until dry.

⚠️ Warnings 58 words ▾

For external use only. FLAMMABLE. Keep away from heat or flames. Avoid contact with eyes. If eye contact occurs, flush with water. Stop use if, in rare instances, redness or irritation develop. If condition persists for more than 72 hours, consult a physician. Keep out of reach of children. If swallowed, contact a physician or poison control center.

🧪 Active Ingredient 5 words ▾

Ethyl Alcohol 62% v/v.......Antibacterial Agent

🧪 Inactive Ingredients 5 words ▾

Water, AMP-C8-18 Perfluoroalkylethyl Phosphate, Glycerin.

🎯 Purpose 17 words ▾

Hand Sanitizer to help reduce bacteria on the skin that could cause disease. Recommended for repeated use.

📄 Keep Out of Reach of Children 15 words ▾

Keep out of reach of children. If swallowed, contact a physician or poison control center.

📄 Package Label / Principal Display Panel 2 words ▾

Principal Display

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 Kutol Products Company. 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 5 other package presentations of this same product, including 50 ml (50865-0688-17), 950 ml (50865-0688-78), 1000 ml (50865-0688-24). 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?
Kutol Products Company 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.
← 50865-0683-04 · Kutol 50865-0710-17 · Kutol →
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.