Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel, 149 mL
by ABC Compounding Co., Inc. · 149 mL in 1 BOTTLE, PLASTIC (62257-061-28)
NDC 62257-0061-28
🏷️ FDA NDC (as labeled)
62257-061-28
billing pads the product segment with a zero
This package
Contains149 mL
Pack sizes10 compare ↓
Also comes in:
2.5 ml 62257-0061-21
118 ml 62257-0061-24
473 ml 62257-0061-47
532 ml 62257-0061-17
800 ml 62257-0061-13
1000 ml 62257-0061-11
1000 ml 62257-0061-12
1200 ml 62257-0061-01
3785 ml 62257-0061-14
OTC
Discontinued
Non-controlled
⚠ Discontinued by firm
🗂️ Data synced Jul 24, 2026 · sources: openFDA · FDA label (DailyMed) · FDA Orange & Purple Book · First Databank · CMS NADAC, ASP, Medicare & Medicaid · RxNorm
📋 All sources & update times →
⚠️
Excluded from the active FDA NDC Directory.
The labeler reported this product as discontinued, so it is excluded from the active NDC Directory. A label may still appear on DailyMed, but the NDC is no longer in the current FDA NDC Directory.
Search the FDA NDC Directory ↗
🆔 Identity & classification
FDA NDC (as labeled)
62257-061-28
Product NDC
62257-061
11-digit billing NDC
62257006128
UNII
3K9958V90M
Application #
M004
SPL Set ID
ee46cb57-c79c-4edf-bc88-4a4f8a95bfc8
DEA schedule
Non-controlled
Marketing category
OTC MONOGRAPH DRUG
Marketing status
Discontinued
FDA listing status
Discontinued by firm
Marketing start
2020-07-20
Route
TOPICAL
Dosage form
GEL
Substance
ALCOHOL
Why two NDCs?
The FDA registers this code as 62257-061-28 — 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 → 62257-0061-28. 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.
🏭 Manufacturer & labeler
LabelerABC Compounding Co., Inc.
FDA applicationM004 (OTC MONOGRAPH DRUG)
Labeler code62257
First marketedJul 2020
Product typeHuman Otc Drug
Portfolio15 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.
🩺 Clinical
📗 Our plain-language guide HelloPharmacist
- Chemically they are related, but hand sanitizer is absolutely not safe to drink — it contains alcohol in concentrations that are toxic if swallowed and often includes other ingredi...
- Is the alcohol in hand sanitizer the same as the alcohol in a drink?
- Yes — most of these products are specifically labeled 'recommended for repeated use.' Just apply enough to cover your hands and rub until dry. If you notice skin irritation or redn...
- Can I use hand sanitizer over and over throughout the day?
Patient education
Supplement & herbal interactions
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.
💬 Questions about ALCOHOL?
Ask a pharmacist →
Ask a licensed pharmacist directly — free, answered by our team.
🧪 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.
💲 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 g | 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. | |
ℹ️
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.
🔁 Therapeutic equivalents
| Product | Labeler | Pack | NADAC/unit | TE | Status | Price vs. this |
|---|---|---|---|---|---|---|
| Jianerkang Sanitizing Wipe .7 mL/mL 34645-0003-01 | Jianerkang | 1 patch | — | — | FDA listed | — |
| Instant Hand Sanitizer STERILE 70 Ethyl Alcohol .7 mL/mL 34645-0007-01 | Jianerkang | 1 patch | — | — | FDA listed | — |
| Zany Antiseptic Gel .7 mL/mL 55715-0004-01 | Laboratorios | 120 ml | — | — | FDA listed | — |
| Antibacterial Hand Sanitizer .7 mL/mL 63710-0001-01 | Laboratorios | 500 ml | — | — | FDA listed | — |
| Zeyco Antiseptic Hand Sanitizer Gel .7 mL/mL 63710-0002-01 | Laboratorios | 125 ml | — | — | FDA listed | — |
| Zeyco Hand Sanitizer .7 mL/mL 63710-0003-01 | Laboratorios | 500 ml | — | — | FDA listed | — |
| Antiseptic Hand Sanitizer .7 mL/mL 63710-0004-00 | Laboratorios | 500 ml | — | — | FDA listed | — |
| Hand Sanitizer .7 mL/mL 67326-0005-00 | Degasa, | 118 ml | — | — | FDA listed | — |
| Protec Hand Sani Gel Antibacterial .7 mL/mL 67326-0006-00 | Degasa, | 118 ml | — | — | FDA listed | — |
| Degasa Hand Sanitizer Lemon Lime Scent .7 mL/mL 67326-0010-02 | Degasa, | 59.14 ml | — | — | FDA listed | — |
| Hand Sanitizer .7 mL/mL 70412-0192-36 | Zhejiang | 236 ml | — | — | FDA listed | — |
| Antibacterial Hand Sanitizer .7 mL/mL 73145-0003-01 | ASC | 30 ml | — | — | FDA listed | — |
| Antibacterial Hand Sanitizer .7 mL/mL 73145-0004-01 | ASC | 236 ml | — | — | FDA listed | — |
| AMBI Soothing Hand sanitizer .7 mL/mL 73453-0143-04 | AMBI | 118 ml | — | — | FDA listed | — |
| Instant Hand Sanitizing Gel .7 mL/mL 77462-0011-01 | SORA | 50 bottles | — | — | FDA listed | — |
| Instant Sanitizing Gel .7 mL/mL 77462-0012-01 | SORA | 500 ml | — | — | FDA listed | — |
| XPRO Antiseptic Hand Sanitizer .7 mL/mL 77939-0000-08 | Savone | 240 ml | — | — | FDA listed | — |
| Cucumber Melon Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0003-01 | Fourstar | 29 ml | — | — | FDA listed | — |
| Fresh Peach Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0004-01 | Fourstar | 29 ml | — | — | FDA listed | — |
| Ocean Breeze Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0005-01 | Fourstar | 29 ml | — | — | FDA listed | — |
| Sweet Pea Scented Antibacterial Hand Sanitizer .7 mL/mL 80684-0006-01 | Fourstar | 29 ml | — | — | FDA listed | — |
| LEMONBELLA Lavender Hand Sanitizer .7 mL/mL 81319-0112-01 | Lemonbella | 100.5 ml | — | — | FDA listed | — |
| Reddy Lab Advanced Alcohol Gel Sanitizer .7 mL/mL 79671-0797-10 | Flavor | 1000 ml | — | — | FDA listed | — |
| Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6006-01 | Professional | 3.23 ml | — | — | FDA listed | — |
| CareALL Hand Sanitizer .7 mL/mL 51824-0110-02 | New | 59 ml | — | — | FDA listed | — |
| Hand-Aid .7 mL/mL 62257-0122-01 | ABC | 1200 ml | — | — | Discontinued | — |
| Han-I-Size Unscented .7 mL/mL 63533-0645-14 | Momar | 3785 ml | — | — | FDA listed | — |
| Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6007-01 | Professional | 484 ml | — | — | FDA listed | — |
| Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6008-01 | Professional | 805.44 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer E3 Gel .7 mL/mL 21749-0711-89 | GOJO | 1200 ml | — | — | FDA listed | — |
| Purell Advanced Soothing .7 mL/mL 21749-0713-01 | GOJO | 30 ml | — | — | Discontinued | — |
| Instant Hand Sanitizer .7 mL/mLthis 62257-0061-28 | ABC | 149 ml | — | — | Discontinued | — |
| PDI Alcohol Prep Pad Sterile Large and Medium .7 mL/mL 10819-3914-01 | Professional | 200 packets | — | — | FDA listed | — |
| PDI Sani-Hands Instant Hand Sanitizing Wipes .7 mL/mL 10819-3916-01 | Professional | 100 packets | — | — | FDA listed | — |
| PURELL Advanced Green Certified Instant Hand Sanitizer .7 mL/mL 21749-0702-08 | GOJO | 237 ml | — | — | Discontinued | — |
| PURELL Professional Advanced Hand Sanitizer Fragrance Free Gel .7 mL/mL 21749-0717-08 | GOJO | 236 ml | — | — | Discontinued | — |
| Genuine First Aid Hand Sanitizer Ethyl Alcohol .7 mL/mL 50814-0060-01 | GFA | 60 ml | — | — | FDA listed | — |
| Genuine First Aid Hand Sanitizer with Cap Ethyl Alcohol .7 mL/mL 50814-0061-01 | GFA | 236 ml | — | — | FDA listed | — |
| Germ Attack Hand Sanitizer .7 mL/mL 66902-0443-02 | Natural | 60 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer be Vibrant .7 mL/mL 21749-0028-01 | GOJO | 30 ml | — | — | FDA listed | — |
| Genuine First Aid Hand Sanitizer Ethyl Alcohol .7 mL/mL 50814-0063-01 | GFA | 473 ml | — | — | FDA listed | — |
| North Woods Derma Gel Clear .7 mL/mL 53125-0801-04 | Superior | 3780 ml | — | — | FDA listed | — |
| Be Smart Get Prepared Hand Sanitizer .7 mL/mL 55550-0611-01 | Total | 1 ml | — | — | FDA listed | — |
| Alcohol Cleansing Wipe .7 mL/mL 83165-0001-00 | Hubei | 1 patch | — | — | FDA listed | — |
| PURELL Healthcare Advanced Hand Sanitizer Gel .7 mL/mL 21749-0716-01 | GOJO | 29 ml | — | — | Discontinued | — |
| Genuine First Aid Hand Sanitizer with Pump Ethyl Alcohol .7 mL/mL 50814-0062-01 | GFA | 236 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer be Blissful .7 mL/mL 21749-0029-01 | GOJO | 30 ml | — | — | FDA listed | — |
| Instant Hand Sanitizer .7 mL/mL 51824-0020-02 | New | 59 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer be Peaceful .7 mL/mL 21749-0027-01 | GOJO | 30 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Naturals Gel .7 mL/mL 21749-0625-01 | GOJO | 30 ml | — | — | FDA listed | — |
| Advanced Alcohol Gel Sanitizer .7 mL/mL 65601-0801-04 | Betco | 3780 ml | — | — | FDA listed | — |
| Tendersant Hand Sanitizer .7 mL/mL 69771-0007-01 | Geri-Gentle | 118 ml | — | — | FDA listed | — |
| Hand Sanitizer .7 mL/mL 70412-0194-15 | Zhejiang | 15 ml | — | — | FDA listed | — |
| Plus Brasept Alcocol Gel .7 mL/mL 83318-0605-14 | NEWDROP | 3785 ml | — | — | Discontinued | — |
| Germ Attack Hand Sanitizer .7 mL/mL 66902-0943-12 | Natural | 3785 ml | — | — | FDA listed | — |
| PURELL Advanced Hand Sanitizer Green Certified Gel .7 mL/mL 21749-0708-08 | GOJO | 237 ml | — | — | FDA listed | — |
| Uline Hand Sanitizer .7 mL/mL 69790-0801-04 | Uline | 3780 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
🏛️
2020
On the market since
Jul 2020
📍
2026
Currently FDA-listed
6 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.
🔬 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 Instant Hand Sanitizer (this brand).
Top reported reactions
Age at onset
Reporter sex
Male · 55%
Female · 45%
Unknown · 0%
Serious outcomes
Reports over time (by year) — tap or hover for the count & year
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.
📦 Packaging — all sizes for this product
| Package NDC | Description | Marketing start | Status |
|---|---|---|---|
| 62257-0061-01 | 1200 mL in 1 CARTRIDGE (62257-061-01) | 2020-12-04 | Discontinued by firm |
| 62257-0061-11 | 1000 mL in 1 BOTTLE, PLASTIC (62257-061-11) | 2020-12-04 | Active |
| 62257-0061-12 | 1000 mL in 1 BAG (62257-061-12) | 2020-12-04 | Discontinued by firm |
| 62257-0061-13 | 800 mL in 1 BAG (62257-061-13) | 2020-12-04 | Discontinued by firm |
| 62257-0061-14 | 3785 mL in 1 BOTTLE, PLASTIC (62257-061-14) | 2020-12-04 | Active |
| 62257-0061-17 | 532 mL in 1 BOTTLE, PLASTIC (62257-061-17) | 2020-12-04 | Active |
| 62257-0061-21 | 2.5 mL in 1 DOSE PACK (62257-061-21) | 2020-12-04 | Discontinued by firm |
| 62257-0061-24 | 118 mL in 1 BOTTLE, PLASTIC (62257-061-24) | 2020-12-04 | Discontinued by firm |
| 62257-0061-28 You're viewing this | 149 mL in 1 BOTTLE, PLASTIC (62257-061-28) | 2020-12-04 | Discontinued by firm |
| 62257-0061-47 | 473 mL in 1 BOTTLE, PLASTIC (62257-061-47) | 2020-12-04 | Active |
Pack size FAQ
What quantity is in NDC 62257-0061-28?
NDC 62257-0061-28 contains 149 mL — 149 ml in 1 bottle, plastic.
What is the difference between NDC 62257-0061-28 and NDC 62257-0061-21?
Both are Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel — the drug itself is identical. NDC 62257-0061-28 is the 149 mL package, while NDC 62257-0061-21 is the 2.5 ml package.
What NDC number is used to bill for this package of Instant Hand Sanitizer ALCOHOL .7 mL/mL Gel?
Bill NDC 62257-0061-28 — the 11-digit billing format is 62257006128. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.
🧭 About this NDC listing & data coverage
Over-the-counter (OTC) product
No longer marketed (per FDA listing data)
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.
What does the discontinued status mean for this NDC?
The labeler reported a marketing end date (or the listing was delisted), so this specific package is no longer actively marketed. Remaining stock may still be dispensed for a time, and the NDC stays valid for historical records and claims — but data feeds (pricing, labeling) typically stop updating for it. Other package sizes or other manufacturers' versions of the same medication may still be marketed — see the equivalents section where available.
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 FDA registers it as 62257-061-28, which is what is printed on the packaging and shown on DailyMed. Insurance claims use a fixed 11-digit 5-4-2 format, so the short segment is padded with a leading zero: 62257-0061-28, written without dashes as 62257006128. The Identity section at the top of this page lists every form of this code.
What do the three segments of this NDC mean?
In 62257-0061-28, the first segment (62257) is the labeler code FDA assigned to ABC Compounding Co., Inc.; the middle segment (0061) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (28) identifies this exact package size and type. Together they name one specific package of one specific product.
Does this product come in other package sizes?
Yes — the FDA directory lists 9 other package presentations of this same product, including 2.5 ml (62257-0061-21), 118 ml (62257-0061-24), 473 ml (62257-0061-47). 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?
ABC Compounding Co., 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.
📄 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
🎯 Indications and Usage ▾
Drug Facts Box OTC-Indications & Usage Section for hand-washing to decrease bacteria on the skin, only when water is not available
⏱️ Dosage and Administration ▾
Drug Facts Box OTC-Dosage & Administration Section wet hands thoroughly with product and allow to dry without wiping
⚠️ Warnings ▾
Drug Facts Box OTC-Warnings Section FLAMMABLE, keep away from fire and flames For external use only
🧪 Active Ingredient ▾
Drug Facts Box OTC-Active Ingredient Section Ethyl Alcohol 70% v/v
🧪 Inactive Ingredients ▾
Drug Facts Box OTC-Inactive Ingredient Section water, DMDM hydantoin, carbomer, propylene glycol, tocopheryl acetate, aloe barbadensis
🎯 Purpose ▾
Drug Facts Box OTC-Purpose Section Antiseptic
No label section mentions that — try another word, or open the full label on DailyMed below.
Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA.
Prefer the government’s original formatting? View this label on DailyMed ↗
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.