WhiskCare 375 Alcohol 600 mL/L Gel, 8 l
by Whisk Products, Inc. · 1 BAG in 1 CARTON (65585-375-01) / .8 L in 1 BAG
NDC 65585-0375-01
🏷️ FDA NDC (as labeled)
65585-375-01
billing pads the product segment with a zero
This package
Contains8 l
Pack sizes15 compare ↓
Also comes in:
1 L 65585-0375-09
1 L 65585-0375-11
1 L 65585-0375-12
1 L 65585-0375-13
1 L 65585-0375-14
1 L 65585-0375-19
3.785 l 65585-0375-05
8 l 65585-0375-10
8 l 65585-0375-17
12 bottles 65585-0375-06
24 bottles 65585-0375-02
059 l 65585-0375-18
203.8 l 65585-0375-16
473 l 65585-0375-15
OTC
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
65585-375-01
Product NDC
65585-375
11-digit billing NDC
65585037501
RxCUI
581658
UNII
3K9958V90M
Application #
505G(a)(3)
SPL Set ID
63c61968-73d7-4d31-9604-e56748b990fa
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2005-06-01
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 65585-375-01 — 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 → 65585-0375-01. 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.
🏭 Manufacturer & labeler
LabelerWhisk Products, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code65585
First marketedJun 2005
Product typeHuman Otc Drug
Portfolio31 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.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- Chemically they are related, but hand sanitizer is absolutely not safe to drink — it contains alcohol in concentrations that are toxic if swallowed and often includes other ingredi...
- Is the alcohol in hand sanitizer the same as the alcohol in a drink?
- Yes — most of these products are specifically labeled 'recommended for repeated use.' Just apply enough to cover your hands and rub until dry. If you notice skin irritation or redn...
- Can I use hand sanitizer over and over throughout the day?
Patient education
Supplement & herbal interactions
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.
💬 Questions about Alcohol?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
💊 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.
💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.
-
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 BR9JLI40NO
A weak organic base used as a pH adjuster and neutralizing agent in liquid formulations. It helps maintain the proper acidity level so the medicine remains stable and effective in its container.
-
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 6DC9Q167V3
Propylene glycol is a clear liquid derived from petroleum or vegetable sources. It acts as a solvent, humectant, and preservative in medicines, helping dissolve active ingredients and maintain product stability.
-
UNII 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, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine
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.
💲 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 system | Per g | Per 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
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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Isagel 600 mL/1000mL 11701-0025-45 | Coloplast | 800 ml | — | — | Discontinued | — |
| Ecolab 60 mL/100mL 47593-0507-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab Facilipro 60 mL/100mL 47593-0508-56 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Ecolab Clear 60 mL/100mL 47593-0638-41 | Ecolab | 750 ml | — | — | Discontinued | — |
| SSDC Gel Hand Sanitizer 60 mL/100mL 47593-0664-70 | Ecolab | 1200 ml | — | — | FDA listed | — |
| Covex Antibacterial Hand Sanitizer, COOL BREEZE .6 mL/mL 51209-0012-00 | DALAN | 236 ml | — | — | FDA listed | — |
| Covex Antibacterial Hand Sanitizer, FRESH ALOE .6 mL/mL 51209-0013-00 | DALAN | 236 ml | — | — | FDA listed | — |
| Amcon Labs Hand Sanitizer Fragrance Free Gel Sanitizer 600 mL/L 51801-0437-08 | Nomax, | 237 l | — | — | FDA listed | — |
| SunDrops 75 .6 mL/mL 63621-0356-14 | Sunburst | 3785 ml | — | — | FDA listed | — |
| Aire-Master Hand Sanitizer 600 mL/L 65585-0358-01 | Whisk | 473 l | — | — | FDA listed | — |
| Sani-Sure 600 mL/L 65585-0359-01 | Whisk | 237 l | — | — | FDA listed | — |
| WhiskCare 375 600 mL/Lthis 65585-0375-01 | Whisk | 8 l | — | — | Discontinued | — |
| WhiskCare 375 Fragrance Free 600 mL/L 65585-0378-01 | Whisk | 8 l | — | — | FDA listed | — |
| Pacific Breeze Instant Hand Sanitizer Gel 600 mL/L 65585-0380-01 | Whisk | 1 l | — | — | FDA listed | — |
| D-Germ 600 mL/L 65585-0498-01 | Whisk | 118 l | — | — | FDA listed | — |
| Algonquin HanSan 600 mL/L 65585-0522-02 | Whisk | 237 l | — | — | FDA listed | — |
| Aire-Master Waterless Hand Sanitizer 600 mL/L 65585-0525-01 | Whisk | 8 l | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2074-01 | Raining | 44 ml | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2075-01 | Raining | 30 ml | — | — | FDA listed | — |
| Unscented Hand Sanitizer 60 mL/100mL 65692-2076-01 | Raining | 59 ml | — | — | FDA listed | — |
| Vindicator Instant Hand Sanitizer 600 mL/1000mL 66608-0515-05 | Kimball | 3785 ml | — | — | Discontinued | — |
| Natural Extensions Fragrance- Free Instant Hand Sanitizer 60 mL/100mL 66975-0101-02 | Benco | 251 ml | — | — | FDA listed | — |
| Applause 3 g/5g 67858-0693-02 | QuestSpecialty | 24 bottles | — | — | FDA listed | — |
| Avant Original - Fragrance Free 60 mL/100mL 68306-0106-01 | B4 | 82.5 ml | — | — | Discontinued | — |
| Zogics Instant Hand Sanitizer Hydrating Gel 60 mL/100mL 72202-0026-01 | Zogics, | 1000 ml | — | — | FDA listed | — |
| palm party 60 mL/100mL 87322-1614-01 | Dongyang | 30 ml | — | — | FDA listed | — |
| Clean and Go 600 mL/1000mL 87377-0001-01 | Satellite | 800 ml | — | — | Discontinued | — |
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
🏛️
2005
On the market since
Jun 2005
📍
2026
Currently FDA-listed
21 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.
🔬 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 375 (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 55%
Female · 45%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 65585-0375-01 You're viewing this | 1 BAG in 1 CARTON (65585-375-01) / .8 L in 1 BAG | 2005-06-01 | Discontinued by firm |
| 65585-0375-02 | 24 BOTTLE, PLASTIC in 1 BOX (65585-375-02) / .118 L in 1 BOTTLE, PLASTIC | 2005-06-01 | Active |
| 65585-0375-05 | 3.785 L in 1 BOTTLE, PLASTIC (65585-375-05) | 2005-11-22 | Active |
| 65585-0375-06 | 12 BOTTLE, PUMP in 1 BOX (65585-375-06) / .237 L in 1 BOTTLE, PUMP | 2006-10-03 | Active |
| 65585-0375-09 | 8 BAG in 1 BOX (65585-375-09) / 1 L in 1 BAG | 2011-10-01 | Discontinued by firm |
| 65585-0375-10 | 12 BAG in 1 BOX (65585-375-10) / .8 L in 1 BAG | 2011-10-11 | Active |
| 65585-0375-11 | 8 BAG in 1 BOX (65585-375-11) / 1 L in 1 BAG | 2011-10-01 | Active |
| 65585-0375-12 | 4 BAG in 1 BOX (65585-375-12) / 1 L in 1 BAG | 2011-10-01 | Active |
| 65585-0375-13 | 6 BAG in 1 BOX (65585-375-13) / 1 L in 1 BAG | 2015-07-16 | Active |
| 65585-0375-14 | 6 BAG in 1 BOX (65585-375-14) / 1 L in 1 BAG | 2016-01-21 | Discontinued by firm |
| 65585-0375-15 | .473 L in 1 BOTTLE, PUMP (65585-375-15) | 2019-01-21 | Active |
| 65585-0375-16 | 203.8 L in 1 DRUM (65585-375-16) | 2020-04-07 | Active |
| 65585-0375-17 | 6 BAG in 1 BOX (65585-375-17) / .8 L in 1 BAG | 2020-06-06 | Active |
| 65585-0375-18 | .059 L in 1 BOTTLE, PLASTIC (65585-375-18) | 2023-10-24 | Active |
| 65585-0375-19 | 4 BAG in 1 BOX (65585-375-19) / 1 L in 1 BAG | 2024-02-22 | Active |
Pack size FAQ
What quantity is in NDC 65585-0375-01?
NDC 65585-0375-01 contains 8 l — 1 bag in 1 carton / .8 l in 1 bag.
What is the difference between NDC 65585-0375-01 and NDC 65585-0375-05?
Both are WhiskCare 375 Alcohol 600 mL/L Gel — the drug itself is identical. NDC 65585-0375-01 is the 8 l package, while NDC 65585-0375-05 is the 3.785 l package.
What NDC number is used to bill for this package of WhiskCare 375 Alcohol 600 mL/L Gel?
Bill NDC 65585-0375-01 — the 11-digit billing format is 65585037501. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 FDA registers it as 65585-375-01, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 65585-0375-01, written without dashes as 65585037501. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 65585-0375-01, the first segment (65585) is the labeler code FDA assigned to Whisk Products, Inc.; the middle segment (0375) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 14 other package presentations of this same product, including 1 l (65585-0375-09), 1 l (65585-0375-11), 1 l (65585-0375-12). 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.
📄 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
🎯 Indications and Usage ▾
Use To help reduce the amount of bacteria on skin
⏱️ Dosage and Administration ▾
Directions Place 5 grams or palmful of product in one hand. Spread on hands and rub into skin until dry. Place a smaller amount (2.5 grams) in one hand and spread over both hands and wrists. Rub into skin until dry. Children should be supervised while using this product.
⚠️ Warnings ▾
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 ▾
Active Ingredient Ethyl Alcohol 60% v/v
🧪 Inactive Ingredients ▾
Inactive Ingredients Water, Glycerin, Fragrance, Carbomer, Propylene Glycol, Diisopropylamine
🎯 Purpose ▾
Purpose Skin Sanitizer
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.