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Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid, 1200 mL — NDC 11084-0807-12 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid, 1200 mL — NDC 11084-807-12 (Billing 11084-0807-12)

by SC Johnson Professional USA, Inc. · 1200 mL in 1 BOTTLE, PLASTIC

This is a package of 1,200 mL of Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid from SC Johnson Professional USA, Inc., marketed since Feb 2018 and currently FDA-listed. It is the main listing for this product, which comes in 7 package sizes.

NDC 11084-0807-12
🏷️ FDA NDC (as labeled) 11084-807-12 billing pads the product segment with a zero
This package
Contains1200 mL Pack sizes7 compare ↓
Main listing for product 11084-807 · Also comes in: 1000 mL 11084-807-67 2 cartridges 11084-807-68 444 ml 11084-807-13 1000 ml 11084-807-27 1000 ml 11084-807-41 1000 ml 11084-807-66
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Jul 24, 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 11084-807-12 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
11084 labeler · 807 product · 12 package
Package marketed since
Apr 1, 2018
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 1108480712 7
FDA record last changed
Jul 24, 2026
⚠️
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-0374-2026
Each entry is an official FDA enforcement report — look up any recall number in the FDA recall database ↗

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11084-807-12
Product NDC 11084-807
11-digit billing NDC 11084080712
UNII F5UM2KM3W7
Application # 505G(a)(3)
SPL Set ID 9ea1175e-45aa-45c5-87a1-55d64cc37a88
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2018-02-01
Route TOPICAL
Dosage form LIQUID
Substance BENZALKONIUM CHLORIDE
Why two NDCs? The FDA registers this code as 11084-807-12 — 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 → 11084-0807-12. 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.

Clinical

🧪 What is this product?

Kindest Kare Advanced Antimicrobial Foam Handwash is a topical liquid foam cleanser containing benzalkonium chloride, a quaternary ammonium compound typically used as an antimicrobial agent in handwashing products. This product is marketed as an over-the-counter drug under FDA's monograph system for antimicrobial hand soaps. Benzalkonium chloride functions as a broad-spectrum antimicrobial to reduce bacteria and certain other microorganisms on the skin during hand cleansing.

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 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: 1000 mL 2 cartridges 444 ml 1000 ml 1000 ml 1000 ml
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
11084-0807-12 You're viewing this Main listing 1200 mL in 1 BOTTLE, PLASTIC 2018-04-01 — Active
11084-0807-13 11084-807-13 444 mL in 1 BOTTLE, PLASTIC 2018-02-01 — Active
11084-0807-27 11084-807-27 1000 mL in 1 BOTTLE, PLASTIC 2018-04-01 — Active
11084-0807-41 11084-807-41 1000 mL in 1 BOTTLE, PLASTIC 2018-02-01 — Active
11084-0807-66 11084-807-66 1000 mL in 1 BOTTLE 2023-02-17 — Active
11084-0807-67 11084-807-67 1 CARTRIDGE in 1 KIT / 1000 mL in 1 CARTRIDGE 2018-02-01 — Active
11084-0807-68 11084-807-68 2 CARTRIDGE in 1 BOX / 1000 mL in 1 CARTRIDGE 2018-02-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1200 mL — 1200 ml in 1 bottle, plastic.
How does this package differ from NDC 11084-0807-13?
Both are Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid — the drug itself is identical. This page's package is the 1200 mL one, while NDC 11084-0807-13 is the 444 ml package.
What NDC number is used to bill for this package of Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid?
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
Kindest Kare Advanced Antimicrobial Foam Handwash .5 mg/100mLthis 11084-0807-12 SC 1200 ml — — FDA listed —
Signatry Antibacterial Plum Foam Handwash .5 mg/100mL 21749-0545-08 GOJO 236 ml — — Discontinued —
Reliable Brand Powered by PURELL Antimicrobial Scented Foam CB10 1.2L .5 mg/100mL 71897-0610-40 Veritiv 1200 ml — — FDA listed —
PURELL Antimicrobial Foaming Hand .5 mg/100mL 21749-0610-40 GOJO 1200 ml — — FDA listed —
Excelon Antibacterial Plum Foam Handwash .5 mg/100mL 21749-0400-08 GOJO 236 ml — — Discontinued —
Primory Antibacterial Plum Foam Handwash .5 mg/100mL 21749-0454-08 GOJO 236 ml — — Discontinued —
GOJO Antibacterial Plum Foam Handwash .5 mg/100mL 21749-0968-08 GOJO 236 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

🏛️
2018
On the market since
Feb 2018
📍
2026
Currently FDA-listed
8 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.

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 T7SWE4S2TT
    Cetyl hydroxyethylcellulose is a thickening agent and film-former made by modifying plant cellulose. It's used in topical medicines to increase texture, improve spreadability, and help create a protective barrier on skin.
  • 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 H2KVQ74JM4
    A compound derived from coconut oil that acts as a conditioning agent and surfactant. It helps stabilize and thicken liquid formulations while reducing static and improving texture in topical products.
  • UNII M4SL82J7HK
    A foaming and cleansing agent derived from coconut oil. It's used in liquid formulations to create texture, improve spreadability, and help distribute active ingredients evenly throughout the product.
  • UNII 21X4Y0VTB1
    A surfactant derived from coconut oil that helps mix oil and water components. It's used in formulations as an emulsifier and foam booster to improve product texture and stability.
  • UNII Z17H97EA6Y
    A plant-derived mild cleanser made from natural sugars and oils. It acts as an emulsifier and surfactant to help mix water and oil-based ingredients together in the medicine.
  • 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 KEH0A3F75J
    Hexylene glycol is a clear liquid alcohol used as a solvent and preservative in medicines. It helps dissolve other ingredients and keeps the product stable during storage.
  • 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 6F36Q0I0AC
    PEG-150 distearate is a waxy substance made by combining polyethylene glycol with stearic acid. It acts as an emulsifier and surfactant to help blend water and oil-based ingredients, and may also function as a thickener or lubricant in the formulation.
  • UNII GIA7T764OD
    A silicone-based ingredient combined with polyethylene glycol. It acts as an emulsifier and surfactant to help blend oils and water-based ingredients, and reduces foaming in liquid formulations.
  • UNII HIE492ZZ3T
    Phenoxyethanol is a synthetic preservative and antimicrobial agent used to prevent bacterial and fungal growth in medicines and cosmetic products, extending shelf life and maintaining product safety.
  • 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 WZH3C48M4T
    Potassium hydroxide is a strong alkaline chemical used in medicines to adjust and maintain the pH level of liquid formulations, helping keep the product stable and the active ingredients effective.
  • UNII 506T60A25R
    Sorbitol is a natural sugar alcohol derived from glucose. It serves as a sweetener, humectant, and bulking agent in medications to improve taste and help maintain moisture in 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.

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

The official label also statesAqua (Water), Hexylene Glycol, Glycerin, PEG-8 Dimethicone, PEG-150 Distearate, Sorbitol, Decyl Glucoside, Soyamidopropyl Amine Oxide, Cocamide MIPA, Cetyl Hydroxyethylcellulose, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Amine Oxide, Lauramine Oxide, Citric Acid, Potassium Hydroxide, Phenoxyethanol.

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

LabelerSC Johnson Professional USA, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code11084
First marketedFeb 2018
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from SC Johnson Professional USA, Inc. labeler code 11084

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 📄 When Using This Product 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Questions or Comments 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 20 words ▾

Uses Healthcare Personnel Handwash to decrease transient bacteria on the skin before contact with patients under medical care or treatments.

⏱️ Dosage and Administration 23 words ▾

Directions Wet hands and apply a small amount of product. Wash hands, rinse thoroughly with water, and repeat as necessary between patient contacts.

⚠️ Warnings 77 words ▾

Warnings For external use only When using this product do not get it in the eyes; causes eye irritation upon direct contact. In case of eye exposure, rinse thoroughly with water. If eye irritation persists, contact a physician.

Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

🧪 Active Ingredient 5 words ▾

Active Ingredient Benzalkonium Chloride 0.50%

🧪 Inactive Ingredients 36 words ▾

Inactive ingredients Aqua (Water), Hexylene Glycol, Glycerin, PEG-8 Dimethicone, PEG-150 Distearate, Sorbitol, Decyl Glucoside, Soyamidopropyl Amine Oxide, Cocamide MIPA, Cetyl Hydroxyethylcellulose, Polyquaternium-7, Cocamidopropyl PG-Dimonium Chloride Phosphate, Cocamidopropyl Amine Oxide, Lauramine Oxide, Citric Acid, Potassium Hydroxide, Phenoxyethanol.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 When Using This Product 33 words ▾

When using this product do not get it in the eyes; causes eye irritation upon direct contact. In case of eye exposure, rinse thoroughly with water. If eye irritation persists, contact a physician.

📄 Stop Use and Ask a Doctor If 18 words ▾

Stop use and ask a doctor if irritation and redness develop and persist for more than 3 days.

📄 Keep Out of Reach of Children 21 words ▾

Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

📄 Questions or Comments 4 words ▾

Questions or comments? 1-866-783-0422

📄 Package Label / Principal Display Panel 74 words ▾

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label SCJ PROFESSIONAL HEALTHCARE Kindest Kare ® NDC 11084-807-27 Hand Soap Antimicrobial Foam Soap Advanced Health Personnel Handwash Moisturizing Fragrance Free Manufactured for : SC Johnson Professional USA, Inc. Charlotte, NC 28217 1-866-783-0422 www.scjp.com Pat. www.scjp.com/patents Made in USA 1 Liter (33.8 fl oz) (1.05 qt) SAP # 4000000171 REORDER # 626461 deb SKIN CARE Open for Drug Facts Principal Display Panel - 1 Liter Bottle Label

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗

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: this package is listed as actively marketed, with no marketing end date reported by SC Johnson Professional USA, 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 cartridge (11084-0807-67), 2 cartridges (11084-0807-68), 444 ml (11084-0807-13). 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?
SC Johnson Professional USA, 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.
← 11084-0803-36 · SC 11084-0908-16 · SC →
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.