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Foaming Instant Hand Sanitizer with Aloe ethanol 70 g/100g Gel, 251 g — NDC 68599-5205-1 (Billing 68599-5205-01)

by MCKESSON MEDICAL-SURGICAL INC. · 251 g in 1 PACKAGE

This is a package of 251 g of Foaming Instant Hand Sanitizer with Aloe ethanol 70 g/100g Gel from MCKESSON MEDICAL-SURGICAL INC., marketed since Jan 2015 and currently FDA-listed. It is the main listing for this product, which comes in 2 package sizes.

NDC 68599-5205-01
🏷️ FDA NDC (as labeled) 68599-5205-1 billing pads the package segment with a zero
This package
Contains251 g Pack sizes2 compare ↓
Main listing for product 68599-5205 · Also comes in: 1000 g 68599-5205-2
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 2026 · this listing last changed Oct 8, 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 68599-5205-1 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
68599 labeler · 5205 product · 1 package
Package marketed since
Oct 24, 2017
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC)
0612479197039, 0612479196421
FDA record last changed
Oct 8, 2026
⚠️
Other active recalls for Ethanol (different manufacturers) — 1 · tap to view
These affect other manufacturers’ products for the same ingredient — not necessarily the exact NDC on this page.
Class II · May 22, 2026 — Microbial contamination of sterile products (Zep Inc) · FDA recall D-0586-2026
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) 68599-5205-1
Product NDC 68599-5205
11-digit billing NDC 68599520501
RxCUI 616805
UNII 3K9958V90M
UPC 0612479197039, 0612479196421
Application # M003
SPL Set ID 5c1f69b7-c8d8-477c-b614-47a3287b0e4c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2015-01-09
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 616805
Why two NDCs? The FDA registers this code as 68599-5205-1 — a 5-4-1 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 package segment → 68599-5205-01. 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 →
4
Nutrient depletion considerations

Ethanol may be associated with lower levels of 4 nutrients — worth a chat with your pharmacist, not a cause for alarm.

🧪 Full Ethanol nutrient depletion report →
An association is not a deficiency. Educational only — don't start or stop anything without professional guidance.
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: 1000 g
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
68599-5205-01 You're viewing this Main listing 251 g in 1 PACKAGE 2017-10-24 — Active
68599-5205-02 68599-5205-2 1000 g in 1 PACKAGE 2017-10-24 — Active

You're viewing the smallest of 2 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 251 g — 251 g in 1 package.
How does this package differ from NDC 68599-5205-02?
Both are Foaming Instant Hand Sanitizer with Aloe ethanol 70 g/100g Gel — the drug itself is identical. This page's package is the 251 g one, while NDC 68599-5205-02 is the 1000 g package.
What NDC number is used to bill for this package of Foaming Instant Hand Sanitizer with Aloe ethanol 70 g/100g 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
PURELL Advanced E3 Rated Instant Hand Sanitizer Foam .7 mL/mL 21749-0802-51 GOJO 550 ml — — Discontinued —
PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0806-51 GOJO 550 ml — — Discontinued —
PURELL Advanced Instant Hand Sanitizer .7 mL/mL 21749-0807-17 GOJO 515 ml — — FDA listed —
PURELL Healthcare Advanced Hand Sanitizer Foam .7 mL/mL 21749-0811-45 GOJO 450 ml — — Discontinued —
PURELL Healthcare Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0822-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Gentle and Free Foam .7 mL/mL 21749-0826-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Fragrance Free Foam .7 mL/mL 21749-0827-17 GOJO 515 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Moisturizing 2in1 Foam 70 mL/100mL 21749-0851-10 GOJO 295 ml — — FDA listed —
PURELL Healthcare Advanced Hand Sanitizer ULTRA NOURISHING Foam .7 mL/mL 21749-0854-53 GOJO 535 ml — — FDA listed —
PURELL Advanced Hand Sanitizer ULTRA NOURISHING Foam 70 mL/100mL 21749-0856-17 GOJO 515 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Naturals Foam 70 mL/100mL 21749-0875-10 GOJO 295 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer Fragrance Free 70 mL/100mL 30805-0020-04 Buckeye 1200 ml — — FDA listed —
Symmetry Foaming Hand Sanitizer 70 mL/100mL 30805-0021-09 Buckeye 1000 ml — — FDA listed —
Altra Foaming Hand Sanitizer Fragrance Free with Aloe and Vitamin E 70 mL/100mL 30805-0023-07 Buckeye 550 ml — — FDA listed —
I-70 Foaming .7 mL/mL 43097-0968-12 People's 1000 ml — — FDA listed —
ESC Protecting Foam Hand Sanitizer 76.9 mL/100mL 47593-0667-41 Ecolab 750 ml — — FDA listed —
Ecolab Retail Foaming Alcohol Hand Sanitizer 70 mL/100mL 47593-0685-56 Ecolab 1200 ml — — FDA listed —
Kay Alcohol Foam Hand Sanitizer 70 mL/100mL 47593-0686-56 Ecolab 1200 ml — — FDA listed —
Tork Hand Sanitizing Alcohol Foam 70 mL/100mL 49351-0301-01 Essity 1000 ml — — FDA listed —
Foaming Hand Sanitizer 70 mL/100mL 50021-0020-01 Empack 550 ml — — FDA listed —
MG FoamSan 70 .7 L/L 50241-0223-02 Morgan 3.785 l — — FDA listed —
EnMotion Foam Hand Sanitizer 70 mL/100mL 54622-0120-01 Georgia-Pacific 1000 ml — — FDA listed —
enMotion Foam High Frequency Use .7 mL/mL 54622-0121-01 Georgia-Pacific 2 bottles — — FDA listed —
Pacific Blue Ultra Foaming Fragrance Free 70 mg/mL 54622-0122-01 Georgia-Pacific 1000 ml — — FDA listed —
Pacific Blue Select Foam Hand Sanitizer, Fragrance Free, Dye Free 70 mL/100mL 54622-0311-01 Georgia-Pacific 24 bottles — — FDA listed —
enMotion Foam High Frequency Use 70 mL/100mL 54622-0486-01 Georgia-Pacific 1000 ml — — FDA listed —
Kleenex Ultra Moisturizing Hand Sanitizer 70 mL/100mL 55118-0530-10 Kimberly-Clark 1000 ml — — Discontinued —
Kleenex Reveal Moisturizing Foam Hand Sanitizer 70 mL/100mL 55118-0531-10 Kimberly-Clark 6 bottles — — Discontinued —
Lynx san a foam .7 mL/mL 62257-0007-10 ABC 1000 ml — — FDA listed —
Fast .7 mL/mL 62257-0658-08 ABC 1000 ml — — Discontinued —
Dermacen Foaming Instant Hand Sanitizer With Aloe 70 mL/100mL 62654-0149-13 Central 1000 ml — — FDA listed —
Saniclean 70 g/100mL 63900-0150-02 Simoniz 1000 ml — — FDA listed —
Foaming Instant Hand Sanitizer with Aloe 70 g/100gthis 68599-5205-01 MCKESSON 251 g — — FDA listed —
Hand Sanitizer 70 mL/100mL 69790-0456-44 Uline 532 ml — — FDA listed —
EXTENDED CARE Foaming Hand Sanitizer .7 mL/mL 71875-0800-40 TRIPLE 1200 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 71897-0465-86 Veritiv 1000 ml — — FDA listed —
Clean Revolution Foaming Hand Sanitizer Refill Supply Container - Gentle and Aloe Enriched - ELIMINATES 99.9% Germs - 70% Ethanol - Ready To Use 70 mL/100mL 74810-0725-00 Replenish 3785 ml — — FDA listed —
Recens Foam .7 mL/mL 75990-0968-07 Certus 700 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 76370-0003-01 Tazza 10000 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 76370-0005-02 Tazza 3785 ml — — Discontinued —
Tazza 70% Alcohol-Based Hand Sanitizing Foam 70 L/100L 76370-0033-00 Tazza 3.785 l — — FDA listed —
Hand Sanitizer Foam 70 mL/100mL 77955-0002-02 Custom 1000 ml — — FDA listed —
Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0101-12 Archer 1000 ml — — FDA listed —
Black Ops 70 Percent Alcohol Foaming Skin Sanitizer 70 mL/100mL 79016-0102-12 Archer 1000 ml — — FDA listed —
KleenLine Essentials Foaming Hand Sanitizer .7 mL/mL 79258-0802-29 Brady 1000 ml — — FDA listed —
MyHealth Advanced Hand Sanitizer 70 mL/100mL 80661-0002-01 Aeroflex 150 ml — — FDA listed —
Novo Foaming Instant Hand Sanitizer .7 mL/mL 81551-0802-04 Noble 3785 ml — — FDA listed —
Foaming Hand Alcohol Foam 70 mL/100mL 83019-0102-11 Draco 1000 ml — — FDA listed —
Premium Hand Sanitizer 70 g/100g 68599-5201-01 MCKESSON 118 g — — Discontinued —
Premium Hand Sanitizer with Aloe 70 g/100g 68599-5202-01 MCKESSON 59 g — — 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

🏛️
2015
On the market since
Jan 2015
📍
2026
Currently FDA-listed
11 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

LabelerMCKESSON MEDICAL-SURGICAL INC.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code68599
First marketedJan 2015
Product typeHuman Otc Drug
Portfolio16 products on file

More NDCs from MCKESSON MEDICAL-SURGICAL INC. labeler code 68599

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 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 15 words ▾

McKesson Foaming Hand Sanitizer with Aloe With Moisturizers & Emollients With Pump for frequent use.

⏱️ Dosage and Administration 16 words ▾

Directions Wet hands thoroughly with product. Allow to dry without wiping. Use no water or towels.

⚠️ Warnings 45 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 for 15 minutes. Discontinue use and see a doctor if irritation occurs. Avoid contact with broken skin.

🧪 Active Ingredient 8 words ▾

Active Ingredient Purpose Ethanol 70% .................................................... hand sanitizer

🧪 Inactive Ingredients 22 words ▾

Inactive Ingredients Aloe Barbadensis Leaf Juice, Caprylyl Glycol, Fragrance, Glycerin, Glyceryl Laurate, Isopropyl Myristate, PEG-10 Dimethicone, Phenoxyethanol, Water, (may contain Citric Acid).

🎯 Purpose 23 words ▾

Uses an antiseptic hand sanitizer for topical application. helps prevent infection and cross-contamination. reduces transient microorganisms on intact skin. recommended for repeated use.

📄 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 2 words ▾

8.5 1000

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

Reported adverse events (FAERS)

Read carefully: FAERS reports are voluntary and unverified. Counts are not incidence, do not establish causation, are subject to reporting bias, and cannot be used to compare one drug to another. Shown for signal context only. Reports for Foaming Instant Hand Sanitizer with Aloe (this brand).

Top reported reactions

Completed Suicide2,795
Toxicity To Various Agents1,744
Drug Abuse1,625
Death1,131
Cardiac Arrest841
Cardio-respiratory Arrest806
Respiratory Arrest762

Reporter sex

7,947 reports
Male · 53%
Female · 47%
Unknown · 1%

Serious outcomes

Death6,940
Disabling15
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 1 0
Most recent year is provisional (FAERS lags ~3 months).
Where does this data come from?
Adverse-event reports from the FDA Adverse Event Reporting System (FAERS) via openFDA. FAERS reports are voluntary and unverified — counts are not incidence and don’t establish causation.

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 MCKESSON MEDICAL-SURGICAL 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 1 other package presentation of this same product, including 1000 g (68599-5205-02). 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?
MCKESSON MEDICAL-SURGICAL 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.
← 68599-5204-01 · Mckesson 68599-5207-01 · McKesson →
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.