WhiskCare 357 Benzalkonium Chloride 1 mg/mL Soap
by Whisk Products, Inc. · 4 BAG in 1 BOX (65585-557-09) / 1000 mL in 1 BAG
NDC 65585-0557-09
🏷️ FDA NDC (as labeled)
65585-557-09
billing pads the product segment with a zero
This package
Contains1000 mL in 1 bag
Pack sizes9 compare ↓
Also comes in:
6 bottles 65585-0557-02
6 bottles 65585-0557-04
6 bottles 65585-0557-07
50 ml 65585-0557-01
1000 ml 65585-0557-03
1000 ml 65585-0557-08
3785 ml 65585-0557-05
208198 ml 65585-0557-06
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 →
⚠️
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · Apr 8, 2026 — CGMP Deviations: product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0693-2026
Class II · Apr 8, 2026 — CGMP Deviations; product manufactured in the same facility under the same conditions as the product found to be contaminated (Blaine Labs Inc) · FDA recall D-0699-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0375-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0369-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0365-2026
Class II · Jan 20, 2026 — CGMP Deviations (ACME UNITED CORPORATION) · FDA recall D-0360-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗
🆔 Identity & classification
FDA NDC (as labeled)
65585-557-09
Product NDC
65585-557
11-digit billing NDC
65585055709
RxCUI
1233282
UNII
F5UM2KM3W7
Application #
505G(a)(3)
SPL Set ID
6d423304-de27-402c-9b18-99ab22b457e0
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
On market
FDA listing status
Listed (active directory)
Marketing start
2020-03-25
Marketing end
2027-06-30
Route
TOPICAL
Dosage form
SOAP
Substance
BENZALKONIUM CHLORIDE
Why two NDCs?
The FDA registers this code as 65585-557-09 — 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 → 65585-0557-09. 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.
🏷️ RxNorm drug class
This medicine belongs to the Quaternary ammonium compounds class.
Drug family (ATC)
Quaternary ammonium compounds, Medicated dressings with antiinfectives, Antiseptics
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 2020
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 357 is an over-the-counter topical soap that contains benzalkonium chloride, a type of antimicrobial agent. Benzalkonium chloride is commonly used in cleansing products for its ability to reduce bacteria and other microorganisms on the skin. This product is marketed as an OTC monograph drug, meaning it follows FDA's established rules for this category of antimicrobial soap rather than undergoing individual product review.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Benzalkonium Chloride — tap one for details:
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 Benzalkonium Chloride?
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 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 4F6FC4MI8W
Lauramine oxide is a surfactant, a substance that helps mix oil and water together. It's used in medicines to improve how ingredients blend and to help the product dissolve or spread properly.
-
UNII YM0K64F20V
A synthetic emulsifier derived from polyethylene glycol and glucose. It helps blend oil and water-based ingredients together and improves the texture and spreadability of the product.
-
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.
4 inactive ingredients listed in the exact product block matched to this NDC.
The official label also statesWater, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate
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 |
|---|---|---|---|---|---|---|
| g and h Protect Hand 1 mg/mL 10056-0026-00 | Access | 250 ml | — | — | FDA listed | — |
| Summit 367 Antibacterial Foam 1 mg/mL 23590-0200-10 | R.L. | 850 ml | — | — | FDA listed | — |
| Summit E2 1 mg/mL 23590-0300-10 | R.L. | 850 ml | — | — | FDA listed | — |
| Swisher 1 mg/mL 47593-0592-41 | Ecolab | 750 ml | — | — | FDA listed | — |
| Swisher TF 1 mg/mL 47593-0601-26 | Ecolab | 1000 ml | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Refill Vanilla Passion Flower .5 g/444g 57337-0045-01 | Rejoice | 444 g | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Refill Wild Berry Blast .5 g/444g 57337-0046-01 | Rejoice | 444 g | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Vanilla Passion Flower .2 g/221g 57337-0047-01 | Rejoice | 221 g | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Wild Berry Blast .2 g/221g 57337-0048-01 | Rejoice | 221 g | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Pink Cherry Blossom .2 g/221g 57337-0049-01 | Rejoice | 221 g | — | — | FDA listed | — |
| XtraCare Foam Antibacterial Hand Wash Refill Pink Cherry Blossom .5 g/444g 57337-0050-01 | Rejoice | 444 g | — | — | FDA listed | — |
| SunDrops 87 1 mg/mL 63621-0387-14 | Sunburst | 3785 ml | — | — | Discontinued | — |
| WhiskCare 387 1 mg/mL 65585-0513-01 | Whisk | 50 ml | — | — | FDA listed | — |
| Algonquin HanClean Foam 1 mg/mL 65585-0520-01 | Whisk | 4000 ml | — | — | FDA listed | — |
| FOAM-BAC Antibacterial Hand 1 mg/mL 65585-0521-01 | Whisk | 1000 ml | — | — | FDA listed | — |
| Algonquin HanClean Foam 1 mg/mL 65585-0530-01 | Whisk | 4000 ml | — | — | FDA listed | — |
| WhiskCare 387 1 mg/mL 65585-0531-01 | Whisk | 50 ml | — | — | FDA listed | — |
| WhiskCare 357 1 mg/mLthis 65585-0557-09 | Whisk | 1000 ml | — | — | FDA listed | — |
| WhiskCare 357 1 mg/mL 65585-0558-01 | Whisk | 50 ml | — | — | FDA listed | — |
| Jade Antibacterial Hand 1 mg/mL 65585-0586-01 | Whisk | 900 ml | — | — | FDA listed | — |
| Natural Extensions Antibacterial Foaming Hand 1 mg/mL 66975-0104-01 | Benco | 3785 ml | — | — | FDA listed | — |
| Aterra7 Antibacterial Foaming Hand 1 mg/mL 68306-0115-01 | B4 | 530 ml | — | — | FDA listed | — |
| Aterra7 Antibacterial Foaming Hand Fragrance Free 1 mg/mL 68306-0117-01 | B4 | 3785 ml | — | — | FDA listed | — |
| Germ-Free 24 Sanitizing 1 mg/mL 71884-0026-01 | Enviro | 245 ml | — | — | FDA listed | — |
| My-Shield Sanitizing 1 mg/mL 71884-0040-01 | Enviro | 244 ml | — | — | FDA listed | — |
| Doctor Inks Sanitizing 1 mg/mL 71884-0200-01 | Enviro | 118 ml | — | — | FDA listed | — |
| Hustle Butter Antibacterial Foaming .1 g/100mL 72014-0200-07 | H.B.D. | 207 ml | — | — | Discontinued | — |
| Lavex Foaming Antibacterial Hand 1 mg/mL 81551-0387-01 | Clark | 1000 ml | — | — | FDA listed | — |
| Foamy Blue 1 mg/mL 83188-0405-04 | Pro | 1000 ml | — | — | FDA listed | — |
| FloraMedis Hand Sanitizer .1 g/100mL 87215-0001-01 | Sichuan | 450 ml | — | — | FDA listed | — |
| GERMisept Antibacterial Hand Sanitizing Wipes 1 mg/mL 70335-0012-01 | Innovent | 200 patches | — | — | FDA listed | — |
| New Wave Cleaning Solutions Foaming Hand Sanitizer 1 mg/mL 80042-0003-00 | NEW | 3785 ml | — | — | FDA listed | — |
| Theraplus Antibacterial Wipes Fresh Scent with Aloe and Vitamin E 1 mg/mL 80684-0007-20 | Fourstar | 20 patches | — | — | Discontinued | — |
| SunDrops 77 1 mg/mL 63621-0354-70 | Sunburst | 6 bottles | — | — | Discontinued | — |
| MyTerra Hand Sanitizer Foam NA 1 mg/mL 70780-0151-13 | PortionPac | 1000 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
🏛️
2020
On the market since
Mar 2020
📍
2026
Currently FDA-listed
6 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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 65585-0557-01 | 50 mL in 1 BOTTLE, PUMP (65585-557-01) | 2020-03-25 | Discontinued by firm |
| 65585-0557-02 | 6 BOTTLE, PUMP in 1 BOX (65585-557-02) / 500 mL in 1 BOTTLE, PUMP | 2020-03-25 | Discontinued by firm |
| 65585-0557-03 | 8 BAG in 1 BOX (65585-557-03) / 1000 mL in 1 BAG | 2020-03-25 | Discontinued by firm |
| 65585-0557-04 | 6 BOTTLE, PUMP in 1 BOX (65585-557-04) / 1750 mL in 1 BOTTLE, PUMP | 2020-03-25 | Active |
| 65585-0557-05 | 3785 mL in 1 BOTTLE, PLASTIC (65585-557-05) | 2020-03-25 | Discontinued by firm |
| 65585-0557-06 | 208198 mL in 1 DRUM (65585-557-06) | 2020-03-25 | Discontinued by firm |
| 65585-0557-07 | 6 BOTTLE, PUMP in 1 BOX (65585-557-07) / 850 mL in 1 BOTTLE, PUMP | 2020-11-20 | Discontinued by firm |
| 65585-0557-08 | 4 BAG in 1 BOX (65585-557-08) / 1000 mL in 1 BAG | 2021-03-04 | Discontinued by firm |
| 65585-0557-09 You're viewing this | 4 BAG in 1 BOX (65585-557-09) / 1000 mL in 1 BAG | 2024-02-22 | Active |
Pack size FAQ
What quantity is in NDC 65585-0557-09?
NDC 65585-0557-09 is listed by the FDA — 4 bag in 1 box / 1000 ml in 1 bag.
What NDC number is used to bill for this package of WhiskCare 357 Benzalkonium Chloride 1 mg/mL Soap?
Bill NDC 65585-0557-09 — the 11-digit billing format is 65585055709. 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 65585-557-09, 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: 65585-0557-09, written without dashes as 65585055709. 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 65585-0557-09, the first segment (65585) is the labeler code FDA assigned to Whisk Products, Inc.; the middle segment (0557) 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 it is currently marketed — but Whisk Products, Inc. has reported a marketing end date of 2027-06-30, 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 8 other package presentations of this same product, including 6 bottles (65585-0557-02), 6 bottles (65585-0557-04), 6 bottles (65585-0557-07). 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 ▾
Uses Reduces amount of bacteria on hand Recommended for repeated use
⏱️ Dosage and Administration ▾
Directions Pump a small amount of foam into palm of hand. Rub thoroughly over all surfaces of both hands for at least fifteen seconds. Rinse with potable water.
⚠️ Warnings ▾
Warnings For external use only. When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Stop use and ask a doctor if irritation or redness develops, or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
🧪 Active Ingredient ▾
Active Ingredient Benzalkonium Chloride 0.1%
🧪 Inactive Ingredients ▾
Inactive Ingredients Water, Lauramine Oxide, Glycerin, PEG-120 Methyl Glucose Dioleate
🎯 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.