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Alcare Extra Hand Sanitizer Alcohol 80 mL/100mL Solution, 1000 mL — NDC 11084-0006-27 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

Alcare Extra Hand Sanitizer Alcohol 80 mL/100mL Solution, 1000 mL — NDC 11084-006-27 (Billing 11084-0006-27)

by SC Johnson Professional USA, Inc. · 1000 mL in 1 BOTTLE, PLASTIC

This is a package of 1,000 mL of Alcare Extra Hand Sanitizer Alcohol 80 mL/100mL Solution from SC Johnson Professional USA, Inc., marketed since Mar 2017 and currently FDA-listed, this package's marketing is listed to end Dec 2026.

NDC 11084-0006-27
🏷️ FDA NDC (as labeled) 11084-006-27 billing pads the product segment with a zero
This package
Contains1000 mL Pack sizes7 compare ↓
Product page 11084-0006-01 Also comes in: 1000 mL 11084-006-13 2 bottles 11084-006-14 47 ml 11084-006-01 400 ml 11084-006-40 1000 ml 11084-006-12 1000 ml 11084-006-66
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 1, 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 11084-006-27 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
11084 labeler · 006 product · 27 package
Package marketed since
Mar 1, 2017
Package marketing ended
Dec 31, 2026
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 1108400627 8
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 11084-006-27
Product NDC 11084-006
11-digit billing NDC 11084000627
RxCUI 1039339
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID b1c8e5d0-a766-4bf0-a385-b7b8940a0e2c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2017-03-01
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1039339
Why two NDCs? The FDA registers this code as 11084-006-27 — 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 → 11084-0006-27. 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 Other antiseptics and disinfectants class.

Drug family (ATC) Other antiseptics and disinfectants, Antidotes, Nerve depressants
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.

Clinical

📗 Our plain-language guide HelloPharmacist
  • It depends on the product. Hand sanitizers and wipes help reduce bacteria on your skin, and alcohol pads prepare skin before an injection. A separate injected form is used by heart...
  • Most directions say to cover all surfaces of your hands and rub until dry. Sprays and wipes follow similar steps. Check your product's label, since directions differ a bit between...
  • Children under 6 should use hand sanitizer only with adult supervision to avoid swallowing. Keep all products out of reach of children. If someone swallows it, get medical help or...
  • Stop using it and ask a doctor if you get irritation and redness, or if your condition lasts more than 72 hours. Avoid broken skin and keep it out of your eyes. If it gets in your...
📖 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.

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 bottles 47 ml 400 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
11084-0006-01 11084-006-01 Main listing 47 mL in 1 BOTTLE, PLASTIC 2017-03-01 — Active
11084-0006-12 11084-006-12 1000 mL in 1 BOTTLE, PLASTIC 2017-03-01 — Active
11084-0006-27 You're viewing this 1000 mL in 1 BOTTLE, PLASTIC 2017-03-01 Dec 31, 2026 Active
11084-0006-40 11084-006-40 400 mL in 1 BOTTLE, PLASTIC 2017-03-01 — Active
11084-0006-66 11084-006-66 1000 mL in 1 BOTTLE 2023-02-17 — Active
11084-0006-13 11084-006-13 1 BOTTLE, PLASTIC in 1 KIT / 1000 mL in 1 BOTTLE, PLASTIC 2025-11-01 — Active
11084-0006-14 11084-006-14 2 BOTTLE, PLASTIC in 1 BOX / 1000 mL in 1 BOTTLE, PLASTIC 2025-11-01 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1000 mL — 1000 ml in 1 bottle, plastic.
How does this package differ from NDC 11084-0006-01?
Both are Alcare Extra Hand Sanitizer Alcohol 80 mL/100mL Solution — the drug itself is identical. This page's package is the 1000 mL one, while NDC 11084-0006-01 is the 47 ml package.
What NDC number is used to bill for this package of Alcare Extra Hand Sanitizer Alcohol 80 mL/100mL Solution?
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
Alcare Extra Hand Sanitizer 80 mL/100mLthis 11084-0006-27 SC 1000 ml — — FDA listed —
ProGel Max Hand Sanitizer 80 mL/100mL 66353-0117-01 Delta 350 ml — — FDA listed —
PSSI E-San .08 L/.1L 69886-0111-03 Safe 189.27 l — — FDA listed —
Hand Sanitizer 80 mL/100mL 75214-0502-12 HANUL 120 ml — — FDA listed —
Hand Sanitizer 80 mL/100mL 77556-0580-01 Astera 30 ml — — FDA listed —
Latalia Alcohol Antiseptic 80 Sanitizing 80 mL/100mL 80016-0004-00 INTERNATIONAL 200 ml — — FDA listed —
Latalia Alcohol Antiseptic 80% Sanitizing 80 mL/100mL 80016-0005-01 INTERNATIONAL 55 ml — — FDA listed —
StellaLife Hand Sanitizer 80 mL/100mL 69685-0201-02 StellaLife, 2 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

🏛️
2017
On the market since
Mar 2017
📍
2026
Currently FDA-listed
9 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.

🧪 Avoiding an ingredient? See Alcohol inactive ingredients by manufacturer: every current product's list side by side, so you can ask your pharmacy for the version that does not list it.

Loading inactive ingredients from the official FDA label in the background. No external source is being called by this page request.
Where does this data come from?
Source: official FDA Structured Product Labeling (SPL) via DailyMed and the openFDA label index. Structured IACT rows and label-wide narrative are kept separate; availability and product-level specificity depend on the submitted label.

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 marketedMar 2017
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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 When Using This Product 📄 Keep Out of Reach of Children 📖 Instructions for Use 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 10 words ▾

Uses for hand sanitizing to reduce bacteria on the skin

⏱️ Dosage and Administration 13 words ▾

Directions apply foaming sanitizer to cover hands rub into skin no rinsing required

⚠️ Warnings 47 words ▾

Warnings For external use only Flammable: Keep away from fire or flame. When using this product avoid contact with eyes. In case of eye contact, flush with water. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 7 words ▾

Flammable: Keep away from fire or flame.

🧪 Active Ingredient 6 words ▾

Active ingredient ETHYL ALCOHOL, 80% w/w

🧪 Inactive Ingredients 23 words ▾

Inactive ingredients AQUA (WATER), BIS-PEG-12 DIMETHICONE, CITRIC ACID, COCO-GLUCOSIDE, DIHYDROXYPROPYL PEG-5 LINOLEAMMONIUM CHLORIDE, GLYCERYL OLEATE, PANTHENOL, PEG-200 HYDROGENATED GLYCERYL PALMITATE, PEG-7 GLYCERYL COCOATE

🎯 Purpose 2 words ▾

Purpose Antibacterial

📄 When Using This Product 16 words ▾

When using this product avoid contact with eyes. In case of eye contact, flush with water.

📄 Keep Out of Reach of Children 19 words ▾

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

📖 Instructions for Use 4 words ▾

For external use only

📄 Package Label / Principal Display Panel 72 words ▾

PRINCIPAL DISPLAY PANEL - 1 Liter Bottle Label SCJ PROFESSIONAL HEALTHCARE Alcare ® NDC 11084-006-12 Hand Sanitizer Foaming Hand Sanitizer Extra Contains Skin Moisturizer 15 seconds Fast-acting CHG Compatible Pat.www.scjp.com/patents SC Johnson Professional USA, Inc. Charlotte, NC 28217 1-866-783-0422 www.scjp.com Made in Canada 1 Liter (33.8 fl oz) SAP # 4000013140 L-1483-R1 / 1000011952 REORDER # 101531 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) — 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.
“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 bottle (11084-0006-13), 2 bottles (11084-0006-14), 47 ml (11084-0006-01). 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.
← 11071-0931-01 · Eisai 11084-0009-01 · 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.