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Instant Hand Sanitizer alcohol 665 mL/1000mL Gel, 1.68 mL — NDC 0404-5988-02 (Billing 00404-5988-02)

by Henry Schein, Inc. · 1.68 mL in 1 POUCH

This is a package of 1.68 mL of Instant Hand Sanitizer alcohol 665 mL/1000mL Gel from Henry Schein, Inc., marketed since Feb 2012 and currently FDA-listed.

NDC 00404-5988-02
🏷️ FDA NDC (as labeled) 0404-5988-02 billing pads the labeler segment with a zero
This package
Contains1.68 mL Pack sizes4 compare ↓
Product page 00404-5988-01 Also comes in: 237 ml 0404-5988-03 473 ml 0404-5988-04 800 ml 0404-5988-01
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

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 0404-5988-02
Product NDC 0404-5988
11-digit billing NDC 00404598802
RxCUI 616762
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 3b075cdc-509d-4259-99a2-0e219998949d
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2012-02-07
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616762
Why two NDCs? The FDA registers this code as 0404-5988-02 — a 4-4-2 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 labeler segment → 00404-5988-02. 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 gPer 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: 237 ml 473 ml 800 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
00404-5988-01 0404-5988-01 Main listing 800 mL in 1 BOX 2012-02-07 — Active
00404-5988-02 You're viewing this 1.68 mL in 1 POUCH 2012-02-07 — Active
00404-5988-03 0404-5988-03 237 mL in 1 BOTTLE, PUMP 2012-02-07 — Active
00404-5988-04 0404-5988-04 473 mL in 1 BOTTLE, PUMP 2012-02-07 — Active

Pack size FAQ

What quantity is in this package?
This package contains 1.68 mL — 1.68 ml in 1 pouch.
How does this package differ from NDC 00404-5988-03?
Both are Instant Hand Sanitizer alcohol 665 mL/1000mL Gel — the drug itself is identical. This page's package is the 1.68 mL one, while NDC 00404-5988-03 is the 237 ml package.
What NDC number is used to bill for this package of Instant Hand Sanitizer alcohol 665 mL/1000mL Gel?
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
Instant Hand Sanitizer 665 mL/1000mLthis 00404-5988-02 Henry 1.68 ml — — FDA listed —
Instant Hand Sanitizer 665 mL/1000mL 00404-5991-01 Henry 800 ml — — FDA listed —
First Aid Only Instant Hand Sanitizer 665 mL/L 00924-0450-00 Acme 034 l — — FDA listed —
First Aid Direct Hand Sanitizer 66.5 g/100g 42961-0123-02 Cintas 10 packets — — FDA listed —
Hand Sanitizer 540.26 g/L 47682-0511-12 Unifirst 10 packets — — FDA listed —
Be Smart Get Prepared Hand Sanitizer .665 mL/mL 55550-0106-02 Total 1 ml — — Discontinued —
Instant Hand Sanitizer 665 mL/L 61010-1112-00 Safetec 046 l — — FDA listed —
Instant Hand Sanitizer 665 mg/L 61010-5111-00 Safetec 1026 l — — FDA listed —
Instant Hand Sanitizer 665 mg/L 61010-8700-01 Safetec 8 l — — FDA listed —
McKesson Antiseptic Hand Sanitizer 665 g/L 68599-1120-01 McKesson 144 packets — — FDA listed —
Antiseptic 666 mg/mL 72663-0111-23 Welly 9 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

🏛️
2012
On the market since
Feb 2012
📍
2026
Currently FDA-listed
14 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.

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

LabelerHenry Schein, Inc.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code00404
First marketedFeb 2012
Product typeHuman Otc Drug
Portfolio172 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.

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 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 12 words ▾

Uses for handwashing to decrease bacteria on skin without soap and water

⏱️ Dosage and Administration 29 words ▾

Directions place a small amount and rub over both hands & wrists until dry allow to dry without wiping children under 6 should be supervised while using this product

⚠️ Warnings 65 words ▾

Warnings For external use only. Flammable, keep away from fire or flame When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water Stop use and ask doctor if irritation and redness develops and 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 5 words ▾

Active Ingredient Ethyl Alcohol 66.5%

🧪 Inactive Ingredients 21 words ▾

Inactive Ingredients aloe vera, carbomer, fragrance, purified water, triethanolamine Distributed by HENRY SCHEIN, INC. Melville, NY 11747 USA Made in U.S.A.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 When Using This Product 17 words ▾

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water

📄 Stop Use and Ask a Doctor If 17 words ▾

Stop use and ask doctor if irritation and redness develops and persists for more than 72 hours

📄 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

📄 Package Label / Principal Display Panel 76 words ▾

PRINCIPAL DISPLAY PANEL – 800 mL Box Label Henry Schein 112-5988 Maxiclens Instant Hand Sanitizer NDC 0404-5988-01

27.05FL. OZ. (800 ML) PRINCIPAL DISPLAY PANEL – 800 mL Box Label

PRINCIPAL DISPLAY PANEL – 1.68 mL Pouch Henry Schein Maxiclens Instant Hand Sanitizer Citrus Scent To Order: Contact your Henry Schein Sales Rep 0.0570 fl.oz. (1.68 ML) Distributed by HENRY SCHEIN, Inc. Melville, NY 11747 USA Made in U.S.A. PRINCIPAL DISPLAY PANEL – 1.68 mL Pouch

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 — Not published for this NDC No photo available yet for this listing.
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 Henry Schein, 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 3 other package presentations of this same product, including 237 ml (00404-5988-03), 473 ml (00404-5988-04), 800 ml (00404-5988-01). 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?
Henry Schein, 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.
← 00404-5987-01 · Henry 00404-5990-01 · Henry →
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.