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WhiskCare 373 Alcohol 620 mL/L Soap, 3.785 l — NDC 65585-0374-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

WhiskCare 373 Alcohol 620 mL/L Soap, 3.785 l — NDC 65585-374-02 (Billing 65585-0374-02)

by Whisk Products, Inc. · 3.785 L in 1 BOTTLE, PLASTIC

This is a package of 3.785 l of WhiskCare 373 Alcohol 620 mL/L Soap from Whisk Products, Inc., marketed since Jun 2022 and currently FDA-listed, this package's marketing is listed to end Jun 2028.

NDC 65585-0374-02
🏷️ FDA NDC (as labeled) 65585-374-02 billing pads the product segment with a zero
This package
Contains3.785 l Pack sizes12 compare ↓
Product page 65585-0374-01 Also comes in: 1 L 65585-374-01 1 L 65585-374-04 1 L 65585-374-05 1 L 65585-374-08 05 l 65585-374-06 05 l 65585-374-10 6 bottles 65585-374-03 6 bottles 65585-374-09 24 bottles 65585-374-07 24 bottles 65585-374-11 208.2 l 65585-374-12
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Aug 13, 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 65585-374-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
65585 labeler · 374 product · 02 package
Package marketed since
Jun 17, 2022
Package marketing ended
Jun 30, 2028
Sample package
No — commercial package
Barcode (UPC-A, from the NDC)
3 6558537402 2
FDA record last changed
Aug 13, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 65585-374-02
Product NDC 65585-374
11-digit billing NDC 65585037402
RxCUI 616763
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID cce95a6a-1188-4c69-8f20-4a1670c4c09b
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-06-17
Marketing end 2028-09-30
Route TOPICAL
Dosage form SOAP
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616763
Why two NDCs? The FDA registers this code as 65585-374-02 — 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 → 65585-0374-02. 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 eachPer 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: 1 L 1 L 1 L 1 L 05 l 05 l 6 bottles 6 bottles 24 bottles 24 bottles 208.2 l
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
65585-0374-01 65585-374-01 Main listing 8 BAG in 1 BOX / 1 L in 1 BAG 2022-06-17 — Discontinued by firm
65585-0374-02 You're viewing this 3.785 L in 1 BOTTLE, PLASTIC 2022-06-17 Jun 30, 2028 Active
65585-0374-03 65585-374-03 6 BOTTLE, DISPENSING in 1 BOX / .55 L in 1 BOTTLE, DISPENSING 2022-06-17 — Discontinued by firm
65585-0374-04 65585-374-04 3 BAG in 1 BOX / 1 L in 1 BAG 2022-06-17 — Discontinued by firm
65585-0374-05 65585-374-05 4 BAG in 1 BOX / 1 L in 1 BAG 2022-06-17 Dec 31, 2027 Active
65585-0374-06 65585-374-06 .05 L in 1 BOTTLE, DISPENSING 2022-06-17 — Discontinued by firm
65585-0374-07 65585-374-07 24 BOTTLE, DISPENSING in 1 BOX / .05 L in 1 BOTTLE, DISPENSING 2022-06-17 — Discontinued by firm
65585-0374-08 65585-374-08 4 BAG in 1 BOX / 1 L in 1 BAG 2022-06-17 — Discontinued by firm
65585-0374-09 65585-374-09 6 BOTTLE, PUMP in 1 BOX / .55 L in 1 BOTTLE, PUMP 2022-06-17 Sep 30, 2028 Active
65585-0374-10 65585-374-10 .05 L in 1 BOTTLE, PUMP 2022-06-17 — Discontinued by firm
65585-0374-11 65585-374-11 24 BOTTLE, PUMP in 1 BOX / .05 L in 1 BOTTLE, PUMP 2022-06-17 Dec 31, 2027 Active
65585-0374-12 65585-374-12 208.2 L in 1 DRUM 2024-07-08 Jun 30, 2028 Active

Pack size FAQ

What quantity is in this package?
This package contains 3.785 l — 3.785 l in 1 bottle, plastic.
How does this package differ from NDC 65585-0374-06?
Both are WhiskCare 373 Alcohol 620 mL/L Soap — the drug itself is identical. This page's package is the 3.785 l one, while NDC 65585-0374-06 is the 05 l package.
What NDC number is used to bill for this package of WhiskCare 373 Alcohol 620 mL/L Soap?
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/100mL 50865-0688-09 Kutol 3785 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/Lthis 65585-0374-02 Whisk 3.785 l — — FDA listed —
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

🏛️
2022
On the market since
Jun 2022
📍
2026
Currently FDA-listed
4 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.

What it looks like

Color white
One label can cover several strengths, so colors may be combined — always confirm a loose pill against the dispensed prescription label or a pharmacist.
Where does this data come from?
Physical description (imprint, shape, color, scoring, coating) from this product’s FDA Structured Product Labeling (SPL), mirrored from DailyMed / openFDA.

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 G2R5YO5N3V
    A synthetic fluorinated alcohol used as a surfactant and wetting agent in pharmaceutical formulations. It helps improve how the medicine disperses and spreads within the product for better consistency and absorption.
  • 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 HLB263IJK9
    A synthetic polymer coating made from three acrylic compounds combined together. It forms a protective film on tablets or capsules to control how and when the medicine releases inside the body.
  • 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.

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

The official label also statesWater, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice

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

LabelerWhisk Products, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code65585
First marketedJun 2022
Product typeHuman Otc Drug
Portfolio31 products on file

More NDCs from Whisk Products, Inc. labeler code 65585

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 11 words ▾

Use To help reduce the amount of bacteria on the skin

⏱️ Dosage and Administration 47 words ▾

Directions Pump a small amount of foam into palm of hand. Spread on hands and rub into skin until dry. Place a smaller amount into one hand and spread over both hands and wrists. Run into skin until dry. Children should be supervised while using this product.

⚠️ Warnings 59 words ▾

Warnings Flammable. Keep away from fire or flame. For external use only. If swallowed, seek medical attention. When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately. Stop use and consult a doctor when skin irritation appears and lasts. KEEP OUT OF REACH OF CHILDREN.

🧪 Active Ingredient 6 words ▾

Active Ingredient Ethyl Alcohol 62% v/v

🧪 Inactive Ingredients 13 words ▾

Inactive Ingredients Water, Acrylates/Perfluorohexylethyl Methacrylate Copolymer, Perfluorohexylethyl Alcohol, Glycerin, Aloe Barbadensis Leaf Juice

🎯 Purpose 3 words ▾

Purpose Skin Sanitizer

📄 Keep Out of Reach of Children 6 words ▾

KEEP OUT OF REACH OF CHILDREN.

📄 Package Label / Principal Display Panel 4 words ▾

1 Gallon Product 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 WhiskCare 373 (this brand).

Top reported reactions

Toxicity To Various Agents6,004
Completed Suicide5,433
Drug Abuse5,289
Overdose1,887
Death1,594
Intentional Overdose1,540
Cardio-respiratory Arrest1,346

Age at onset

Neonate26
Infant14
Child16
Adolescent92
Adult2,810
Elderly294

Reporter sex

0 reports

Serious outcomes

Death15,128
Hospitalization8,619
Life-threatening1,403
Disabling212
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,655 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 it is currently marketed — but Whisk Products, Inc. has reported a marketing end date of 2028-09-30, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Does this product come in other package sizes?
Yes — the FDA directory lists 11 other package presentations of this same product, including 1 l (65585-0374-01), 1 l (65585-0374-04), 1 l (65585-0374-05). 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?
Whisk Products, 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.
← 65585-0372-01 · Whisk 65585-0375-01 · Whisk →
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.