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WhiskCare 373 Alcohol 700 mL/L Solution, 6 bottles — NDC 65585-0361-09 package photo

WhiskCare 373 Alcohol 700 mL/L Solution, 6 bottles

by Whisk Products, Inc. · 6 BOTTLE, PUMP in 1 BOX (65585-361-09) / .55 L in 1 BOTTLE, PUMP
NDC 65585-0361-09
🏷️ FDA NDC (as labeled) 65585-361-09 billing pads the product segment with a zero
This package
Contains6 bottles Pack sizes7 compare ↓
Also comes in: 1 L 65585-0361-01 1 L 65585-0361-05 3.785 l 65585-0361-02 05 l 65585-0361-10 24 bottles 65585-0361-11 208.2 l 65585-0361-12
OTC On market Non-controlled
🗂️ Data synced Aug 20, 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

FDA NDC (as labeled) 65585-361-09
Product NDC 65585-361
11-digit billing NDC 65585036109
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 57d5cd5d-8597-ce66-e063-6394a90a0047
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2026-07-31
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 65585-361-09 — 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 → 65585-0361-09. 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.

🏭 Manufacturer & labeler

LabelerWhisk Products, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code65585
First marketedJul 2026
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?
📖 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.

💊 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 RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII ZJ6U4W4J7C
    A silicone-based polymer that helps reduce foam and improve how liquid medicines flow and spread. It works as a surfactant and anti-foaming agent in oral liquids and topical products.
  • UNII VNX7251543
    A plant-derived emulsifier made from coconut oil and polyethylene glycol. It helps mix oil and water-based ingredients together and improves how the medicine spreads or absorbs.
  • 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, Bis-PEG-1- Dimethicone, Propylene Glycol, PEG-7 Glyceryl Cocoate, 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.

💲 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: 1 L 1 L 3.785 l 05 l 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Aire-Master Foaming Hand Sanitizer Fragrance Free 700 mL/L 65585-0532-01 Whisk 3.785 l — — FDA listed —
WhiskCare 373 700 mL/Lthis 65585-0361-09 Whisk 6 bottles — — 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

🏛️
2026
On the market since
Jul 2026
📍
2026
Currently FDA-listed
listed with the FDA
🔒
·
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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
65585-0361-01 8 BAG in 1 BOX (65585-361-01) / 1 L in 1 BAG 2026-07-31 Active
65585-0361-02 3.785 L in 1 BOTTLE, PLASTIC (65585-361-02) 2026-07-31 Active
65585-0361-05 4 BAG in 1 BOX (65585-361-05) / 1 L in 1 BAG 2026-07-31 Active
65585-0361-09 You're viewing this 6 BOTTLE, PUMP in 1 BOX (65585-361-09) / .55 L in 1 BOTTLE, PUMP 2026-07-31 Active
65585-0361-10 .05 L in 1 BOTTLE, PUMP (65585-361-10) 2026-07-31 Active
65585-0361-11 24 BOTTLE, PUMP in 1 BOX (65585-361-11) / .05 L in 1 BOTTLE, PUMP 2026-07-31 Active
65585-0361-12 208.2 L in 1 DRUM (65585-361-12) 2026-07-31 Active

Pack size FAQ

What quantity is in NDC 65585-0361-09?
NDC 65585-0361-09 contains 6 bottles — 6 bottle, pump in 1 box / .55 l in 1 bottle, pump.
What is the difference between NDC 65585-0361-09 and NDC 65585-0361-02?
Both are WhiskCare 373 Alcohol 700 mL/L Solution — the drug itself is identical. NDC 65585-0361-09 is the 6 bottles package, while NDC 65585-0361-02 is the 3.785 l package.
What NDC number is used to bill for this package of WhiskCare 373 Alcohol 700 mL/L Solution?
Bill NDC 65585-0361-09 — the 11-digit billing format is 65585036109. 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
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 FDA registers it as 65585-361-09, 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: 65585-0361-09, written without dashes as 65585036109. 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 65585-0361-09, the first segment (65585) is the labeler code FDA assigned to Whisk Products, Inc.; the middle segment (0361) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (09) identifies this exact package size and type. Together they name one specific package of one specific product.
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 Whisk Products, 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 6 other package presentations of this same product, including 1 l (65585-0361-01), 1 l (65585-0361-05), 3.785 l (65585-0361-02). 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 10 words ▾

Use To help reduce the amount of bacteria on 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. Rub 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 70% v/v

🧪 Inactive Ingredients 14 words ▾

Inactive Ingredients Water, Bis-PEG-1- Dimethicone, Propylene Glycol, PEG-7 Glyceryl Cocoate, Aloe Barbadensis Leaf Juice

🎯 Purpose 3 words ▾

Purpose Skin Sanitizer

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 65585-0360-01 · Whisk 65585-0365-02 · 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.