WhiskCare 365 Chloroxylenol 10 mg/mL Soap, 59 mL
by Whisk Products, Inc. · 59 mL in 1 BOTTLE, PLASTIC (65585-365-13)
NDC 65585-0365-13
🏷️ FDA NDC (as labeled)
65585-365-13
billing pads the product segment with a zero
This package
Contains59 mL
Pack sizes9 compare ↓
Also comes in:
4 bottles 65585-0365-09
6 bottles 65585-0365-08
12 bottles 65585-0365-10
59 ml 65585-0365-04
800 ml 65585-0365-05
1000 ml 65585-0365-11
3785 ml 65585-0365-02
208198 ml 65585-0365-06
OTC
On market
Non-controlled
🗂️ 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 →
🆔 Identity & classification
FDA NDC (as labeled)
65585-365-13
Product NDC
65585-365
11-digit billing NDC
65585036513
RxCUI
413257
UNII
0F32U78V2Q
Application #
505G(a)(3)
SPL Set ID
420f941d-8ed0-42f4-901a-b04b29b51da6
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2000-03-31
Route
TOPICAL
Dosage form
SOAP
Substance
CHLOROXYLENOL
Why two NDCs?
The FDA registers this code as 65585-365-13 — 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 → 65585-0365-13. 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 Phenol and derivatives class.
Drug family (ATC)
Phenol and derivatives
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 marketedMar 2000
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
🧪 What is this product?
WhiskCare 365 Chloroxylenol 10 mg/mL Soap is a topical cleanser containing chloroxylenol, an antimicrobial ingredient commonly used in over-the-counter soaps and body washes. Chloroxylenol is typically used as a germ-fighting agent in personal hygiene products. This is an OTC monograph drug, meaning it is marketed under FDA's established rules for the antimicrobial soap category rather than through an individual product application.
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 Chloroxylenol?
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 2968PHW8QP
A weak organic acid derived from citrus fruits or made through fermentation. It works as a buffer to control pH, a preservative to extend shelf life, and a flavoring agent in medications.
-
UNII MP1J8420LU
A salt derived from edetic acid that binds to trace metals in medicines. It serves as a chelating agent and preservative to prevent metal-catalyzed breakdown of the drug and extend shelf life.
-
UNII ND2M416302
Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
-
UNII I29I2VHG38
A foaming and thickening agent derived from lauric acid (a natural fatty acid). It helps create texture and stability in liquid or semi-solid formulations, often used in topical products.
-
UNII 0L414VCS5Y
A synthetic polymer used as a film-former and conditioning agent. It helps create a protective coating on hair or skin surfaces and improves texture and manageability in topical formulations.
-
UNII O9W3D3YF5U
A synthetic surfactant derived from petroleum-based olefins. It helps dissolve or suspend active ingredients and other substances in liquid formulations, improving how the medicine mixes and flows.
-
UNII BPV390UAP0
Sodium laureth sulfate is a mild detergent and surfactant derived from coconut oil or petroleum. It helps mix oil and water in formulations and is often used as a cleaning or foaming agent in topical products like shampoos and cleansers.
7 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, Sodium C14-16 Olefin Sulfonate, Sodium Laureth Sulfate, Lauramide DEA, Isopropyl Alcohol, Polyquaternium-7, Fragrance, Styrene/Acrylates Copolymer, Tetrasodium EDTA, Citric Acid
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 each | 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 |
|---|---|---|---|---|---|---|
| Kindest Kare Hand Antimicrobial Handwash 1 g/100mL 11084-0036-41 | SC | 1000 ml | — | — | FDA listed | — |
| Acute-Kare Healthcare Personnel Handwash 1 g/100mL 11084-0800-41 | SC | 1000 ml | — | — | FDA listed | — |
| DigiClean E 1 mg/100mL 47593-0308-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Ecolab 10 mg/mL 47593-0506-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| VioNexus 1 g/100mL 55443-0600-03 | Metrex | 2 bottles | — | — | FDA listed | — |
| SoftenSure Foam Antimicrobial 10 mg/mL 59900-0127-05 | Best | 1250 ml | — | — | FDA listed | — |
| Soften Sure Foam Antimicrobial 10 g/1000mL 59900-0211-06 | Best | 1000 ml | — | — | FDA listed | — |
| Prestige 10 mg/mL 63621-0335-14 | Sunburst | 3785 ml | — | — | FDA listed | — |
| FoamyIQ Healthcare Personnel Handwash 10.11 g/L 64009-0203-06 | Spartan | 1.25 l | — | — | FDA listed | — |
| Lite nFoamy Healthcare Personnel Handwash 10.11 g/L 64009-0335-82 | Spartan | 532 l | — | — | FDA listed | — |
| Antiseptic Hand Cleaner 10.11 g/L 64009-0336-85 | Spartan | 3.79 l | — | — | FDA listed | — |
| Clean Xpress Antiseptic Hand Cleaner 10 mg/mL 64009-0338-02 | Spartan | 1000 ml | — | — | FDA listed | — |
| Soft Care Defend Foam Antibacterial Handwash 1 g/100mL 64536-8308-02 | Diversey, | 1200 ml | — | — | Discontinued | — |
| Soft Care Defend Antibacterial Handwash 1 g/100mL 64536-8748-02 | Diversey, | 1200 ml | — | — | Discontinued | — |
| Soft Care Defend Antibacterial Handwash 10 g/L 64536-8760-02 | Diversey, | 3.78 l | — | — | FDA listed | — |
| WhiskCare 365 10 mg/mLthis 65585-0365-13 | Whisk | 59 ml | — | — | FDA listed | — |
| AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL 66949-0139-01 | Zep | 208198 ml | — | — | FDA listed | — |
| AFCO 5508 Sanifect Foam-E II 2081980 mg/208198mL 66949-0141-01 | Zep | 208198 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
🏛️
2000
On the market since
Mar 2000
📍
2026
Currently FDA-listed
26 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 365 (this brand).
Top reported reactions
Reporter sex
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 |
|---|---|---|---|
| 65585-0365-02 | 3785 mL in 1 BOTTLE, PLASTIC (65585-365-02) | 2000-03-31 | Active |
| 65585-0365-04 | 59 mL in 1 TUBE (65585-365-04) | 2000-03-31 | Discontinued by firm |
| 65585-0365-05 | 12 BAG in 1 BOX (65585-365-05) / 800 mL in 1 BAG | 2000-03-31 | Active |
| 65585-0365-06 | 208198 mL in 1 DRUM (65585-365-06) | 2000-03-31 | Active |
| 65585-0365-08 | 6 BOTTLE, PUMP in 1 BOX (65585-365-08) / 1750 mL in 1 BOTTLE, PUMP | 2005-10-13 | Active |
| 65585-0365-09 | 4 BOTTLE, PUMP in 1 BOX (65585-365-09) / 4000 mL in 1 BOTTLE, PUMP | 2005-10-13 | Discontinued by firm |
| 65585-0365-10 | 12 BOTTLE, PUMP in 1 BOX (65585-365-10) / 236.6 mL in 1 BOTTLE, PUMP | 2006-10-03 | Active |
| 65585-0365-11 | 8 BAG in 1 BOX (65585-365-11) / 1000 mL in 1 BAG | 2006-06-16 | Active |
| 65585-0365-13 You're viewing this | 59 mL in 1 BOTTLE, PLASTIC (65585-365-13) | 2023-03-29 | Active |
Pack size FAQ
What quantity is in NDC 65585-0365-13?
NDC 65585-0365-13 contains 59 mL — 59 ml in 1 bottle, plastic.
What is the difference between NDC 65585-0365-13 and NDC 65585-0365-10?
Both are WhiskCare 365 Chloroxylenol 10 mg/mL Soap — the drug itself is identical. NDC 65585-0365-13 is the 59 mL package, while NDC 65585-0365-10 is the 12 bottles package.
What NDC number is used to bill for this package of WhiskCare 365 Chloroxylenol 10 mg/mL Soap?
Bill NDC 65585-0365-13 — the 11-digit billing format is 65585036513. 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 65585-365-13, 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: 65585-0365-13, written without dashes as 65585036513. 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 65585-0365-13, the first segment (65585) is the labeler code FDA assigned to Whisk Products, Inc.; the middle segment (0365) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (13) 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 8 other package presentations of this same product, including 4 bottles (65585-0365-09), 6 bottles (65585-0365-08), 12 bottles (65585-0365-10). 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 reduces amount of bacteria on hands
⏱️ Dosage and Administration ▾
Directions Wet hands and forearms. Apply a small amount (5 mL) or palmful to hands and forearms. Scrub thoroughly for at least fifteen seconds. Rinse completely and dry.
⚠️ Warnings ▾
Warnings For external use only. Do not use in eyes. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a physician. Not for use on children under six months of age. For institutional and professional use only.
🧪 Active Ingredient ▾
Active Ingredient Chloroxylenol 1%
🧪 Inactive Ingredients ▾
Inactive Ingredients Water, Sodium C14-16 Olefin Sulfonate, Sodium Laureth Sulfate, Lauramide DEA, Isopropyl Alcohol, Polyquaternium-7, Fragrance, Styrene/Acrylates Copolymer, Tetrasodium EDTA, Citric Acid
🎯 Purpose ▾
Purpose Skin Antimicrobial
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.