Instant Foam Non-alcohol PURE Hand Sanitizer BENZALKONIUM CHLORIDE .13 g/100mL Liquid, 1000 mL — NDC 11084-300-27 (Billing 11084-0300-27)
This is a package of 1,000 mL of Instant Foam Non-alcohol PURE Hand Sanitizer BENZALKONIUM CHLORIDE .13 g/100mL Liquid from SC Johnson Professional USA, Inc., no longer marketed (first marketed Apr 2015), no longer in the FDA NDC Directory.
NDC database record
One package, one record: these facts belong to NDC 11084-300-27 alone.
- Record
- FDA NDC Directory package listing · Human OTC drug
- Code segments
- 11084 labeler · 300 product · 27 package
- Listing certified through
- Dec 31, 2026
- Barcode (UPC-A, from the NDC)
- 3 1108430027 7
- FDA record last changed
- Jul 24, 2026
Other active recalls for Benzalkonium Chloride (different manufacturers) — 6 · tap to view
Identity & classification
Regulatory identifiers FDA, NLM and CMS codes for this package
- RxCUI (RxNorm): 1020365
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
- RxNorm (NLM RxNav) · catalog refreshed Oct 1, 2026
- Medi-Span GPI (licensed)
- First Databank (licensed) · refreshed Oct 1, 2026
RxNorm drug class
This medicine belongs to the Quaternary ammonium compounds class.
Where does this data come from?
- RxClass (NLM) · catalog refreshed Oct 1, 2026
Clinical
Instant Foam Non-alcohol PURE Hand Sanitizer is a topical liquid foam intended for application to the hands. It contains benzalkonium chloride, an antimicrobial agent typically used in hand sanitizers to reduce bacteria and other microorganisms on the skin. This product is an OTC monograph drug, meaning it is marketed under FDA's established rules for over-the-counter hand sanitizers rather than as an individually reviewed application. The alcohol-free formulation makes it suitable for frequent use on hands.
Patient education
Supplement & herbal interactions
Some supplements/herbs that may interact with Benzalkonium Chloride — tap one for details:
Where does this data come from?
- MedlinePlus (NLM) · refreshed Oct 1, 2026
- FDA label on DailyMed · label index refreshed Oct 6, 2026
Ask a licensed pharmacist directly — free, answered by our team.
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 mL | 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. | |
Where does this data come from?
- CMS NADAC weekly file
- CMS ASP pricing files · refreshed Sep 20, 2026
- CMS Medicaid State Drug Utilization Data · refreshed Oct 6, 2026
- CMS Part D plan pricing files · refreshed Sep 24, 2026
- VA National Acquisition Center price file
Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Marketing end | Status |
|---|---|---|---|---|
| 11084-0300-01 11084-300-01 Main listing | 47 mL in 1 BOTTLE, PLASTIC | 2020-04-15 | — | Discontinued by firm |
| 11084-0300-12 11084-300-12 | 1200 mL in 1 BOTTLE, PLASTIC | 2020-04-15 | — | Active |
| 11084-0300-27 You're viewing this | 1000 mL in 1 BOTTLE, PLASTIC | 2020-04-15 | — | Discontinued by firm |
| 11084-0300-40 11084-300-40 | 400 mL in 1 BOTTLE, PLASTIC | 2020-10-01 | — | Discontinued by firm |
| 11084-0300-97 11084-300-97 | 296 mL in 1 BOTTLE, PLASTIC | 2020-04-15 | — | Discontinued by firm |
| 11084-0300-66 11084-300-66 | 1000 mL in 1 BOTTLE | 2023-02-17 | — | Active |
Pack size FAQ
What quantity is in this package?
How does this package differ from NDC 11084-0300-01?
What NDC number is used to bill for this package of Instant Foam Non-alcohol PURE Hand Sanitizer BENZALKONIUM CHLORIDE .13 g/100mL Liquid?
Therapeutic equivalents
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- FDA Orange Book · refreshed Oct 3, 2026
- CMS NADAC weekly file
Availability & generic status
We did not find an FDA-approved generic match for this exact strength, form and route.
Where does this data come from?
- FDA Orange Book · refreshed Oct 3, 2026
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.
Where does this data come from?
IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.- FDA label on DailyMed · label index refreshed Oct 6, 2026
- FDA openFDA NDC Directory · synced Oct 1, 2026
Inactive ingredient FAQ
Are inactive ingredients the same for every manufacturer?
Why might an inactive ingredient be missing?
Can inactive ingredients matter?
Manufacturer & labeler
More NDCs from SC Johnson Professional USA, Inc. labeler code 11084
- Alcare Antiseptic Handrub ALCOHOL 70 mL/100mL Liquid NDC 11084-035-18
- Kindest Kare Hand Antimicrobial Handwash CHLOROXYLENOL 1 g/100mL Soap NDC 11084-036-41
- Bactoshield CHG Chlorhexidine Gluconate 20 mg/mL Solution NDC 11084-038-03
- Bactoshield CHG CHLORHEXIDINE GLUCONATE 40 mg/mL Solution NDC 11084-039-03
- Bactoshield CHG CHLORHEXIDINE GLUCONATE 20 mg/mL Liquid NDC 11084-126-03
- Bactoshield CHG CHLORHEXIDINE GLUCONATE 40 mg/mL Liquid NDC 11084-128-03
- InstantFoam Complete PURE ALCOHOL 80 g/100mL Liquid NDC 11084-303-01
- InstantFoam Complete PURE ALCOHOL 85.6 mL/100mL Liquid NDC 11084-309-12
- Acute-Kare Healthcare Personnel Handwash CHLOROXYLENOL 1 g/100mL Soap NDC 11084-800-41
- Alcare OR Foamed Antiseptic Handrub ALCOHOL 62 g/100g Aerosol, Foam NDC 11084-802-80
- Alcare Plus Foamed Antiseptic Handrub ALCOHOL 62 g/100g Aerosol, Foam NDC 11084-803-36
- Kindest Kare Advanced Antimicrobial Foam Handwash BENZALKONIUM CHLORIDE .5 mg/100mL Liquid NDC 11084-807-12
Where does this data come from?
- FDA openFDA NDC Directory · synced Oct 1, 2026
- Drugs@FDA
FDA label — Drug Facts FDA SPL
🎯 Indications and Usage ▾
Uses to decrease bacteria on the skin that could cause disease
⏱️ Dosage and Administration ▾
Directions Wet hands thouroughly with product and allow to dry without wiping. For children under 6, use only under adult supervision.
⚠️ Warnings ▾
Warnings For external use only When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if irritation and redness develop 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, 0.13%
🧪 Inactive Ingredients ▾
Inactive ingredients Aqua (Water), Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Cocamidopropyl Betaine, Lauramine Oxide, Phenoxyethanol, Propylene Glycol, Tetrasodium EDTA
🎯 Purpose ▾
Purpose Antiseptic
📄 When Using This Product ▾
When using this product Keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest.
📄 Stop Use and Ask a Doctor If ▾
Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours
📄 Keep Out of Reach of Children ▾
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
📄 Package Label / Principal Display Panel ▾
PRINCIPAL DISPLAY PANEL - 1 L Bottle Label SCJ PROFESSIONAL A Family Company™ NDC 11084-300-27 InstantFOAM™ Non-Alcohol PURE HAND SANITIZER Alcohol-Free FOAM Hand sanitizer - Dye & Perfume-Free Stock #: 55857/4000007087 SC Johnson Professional USA, Inc. Charlotte, NC 28217, 1-800-248-7190 www.scjp.com 1 L (33.8 fl oz) deb SKIN CARE 1000003036/0220 PRINCIPAL DISPLAY PANEL - 1 L Bottle Label
About this NDC listing & data coverage
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) | — Not published for this NDC The labeler did not submit a structured excipient list, or no SPL is 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. |