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H2One Ethyl Alcohol 75 mL/100mL Gel, 237 mL — NDC 75742-0006-01 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

H2One Ethyl Alcohol 75 mL/100mL Gel, 237 mL — NDC 75742-006-01 (Billing 75742-0006-01)

by Zhejiang Guoyao Jingyue Aerosol Co., Ltd. · 237 mL in 1 BOTTLE, PUMP

This is a package of 237 mL of H2One Ethyl Alcohol 75 mL/100mL Gel from Zhejiang Guoyao Jingyue Aerosol Co., Ltd., marketed since Jul 2020 and currently FDA-listed. It is the main listing for this product, which comes in 5 package sizes.

NDC 75742-0006-01
🏷️ FDA NDC (as labeled) 75742-006-01 billing pads the product segment with a zero
This package
Contains237 mL Pack sizes5 compare ↓
Main listing for product 75742-006 · Also comes in: 250 ml 75742-006-03 375 ml 75742-006-02 500 ml 75742-006-04 1000 ml 75742-006-05
OTC On market Non-controlled ⇄ Compare with another NDC
🗂️ FDA directory synced Oct 8, 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 75742-006-01 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
75742 labeler · 006 product · 01 package
Package marketed since
Jul 6, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2027
Barcode (UPC-A, from the NDC)
3 7574200601 7
FDA record last changed
Jul 24, 2026
⚠️
Other active recalls for Ethyl Alcohol (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 23, 2025 — Subpotent product: Product has cloudy appearance and tested below assay label claim for 70% Ethyl Alcohol (Consumer Product Partners, LLC) · FDA recall D-0458-2025
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) 75742-006-01
Product NDC 75742-006
11-digit billing NDC 75742000601
RxCUI 1305100
UNII 3K9958V90M
Application # M003
SPL Set ID a9bcecf7-7767-69b4-e053-2995a90a9247
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-07-06
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1305100
Why two NDCs? The FDA registers this code as 75742-006-01 — 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 → 75742-0006-01. 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 →

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: 250 ml 375 ml 500 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
75742-0006-01 You're viewing this Main listing 237 mL in 1 BOTTLE, PUMP 2020-07-06 — Active
75742-0006-02 75742-006-02 375 mL in 1 BOTTLE, PUMP 2020-07-06 — Active
75742-0006-03 75742-006-03 250 mL in 1 BOTTLE, PUMP 2020-07-06 — Active
75742-0006-04 75742-006-04 500 mL in 1 BOTTLE, PUMP 2020-07-06 — Active
75742-0006-05 75742-006-05 1000 mL in 1 BOTTLE, PUMP 2020-07-06 — Active

You're viewing the smallest of 5 pack sizes for this product.

Pack size FAQ

What quantity is in this package?
This package contains 237 mL — 237 ml in 1 bottle, pump.
How does this package differ from NDC 75742-0006-03?
Both are H2One Ethyl Alcohol 75 mL/100mL Gel — the drug itself is identical. This page's package is the 237 mL one, while NDC 75742-0006-03 is the 250 ml package.
What NDC number is used to bill for this package of H2One Ethyl Alcohol 75 mL/100mL 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
Gold Bond Hydrating Hand Sanitizer 75 mL/100mL 41167-0751-02 Chattem, 147 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 75 mL/100mL 43473-0011-01 Nantong 9 ml — — FDA listed —
My Medic Super Sanitizer 75 mL/100mL 43473-0041-01 Nantong 9 ml — — FDA listed —
Unishield Hand Sanitizer 75 mL/100mL 49314-0004-01 Unishield 25 packets — — FDA listed —
MedPride Instant Sanitizer 75 mL/100mL 52410-4088-02 SHIELD 53 ml — — FDA listed —
Dr. Talbots 75 mL/100mL 70797-0160-01 Talbots 50 ml — — FDA listed —
ER Hand Sanitizer Packets 75 mL/100mL 72976-0016-01 EVER 114 packets — — FDA listed —
Locke Teddy 75 mL/100mL 73928-0001-01 KINGKEY 30 ml — — FDA listed —
Pure care hand sanitizer 75 mL/100mL 73928-0004-01 KINGKEY 59 ml — — FDA listed —
livWell 75 mL/100mL 73928-0005-01 KINGKEY 30 ml — — FDA listed —
Orbit Innovations Hand Sanitizer 75 mL/100mL 73928-0040-01 Kingkey 30 ml — — FDA listed —
Hand Sanitizer .75 mL/mL 74640-0010-30 Gordon 30 ml — — FDA listed —
Platinum Hand Sanitizer with Aloe Vera 75 mL/100mL 75262-0002-01 ZheJiang 200 ml — — Discontinued —
Hand Sanitiser 75 mL/100mL 75742-0001-01 Zhejiang 500 ml — — FDA listed —
Shaboink 75 mL/100mL 75742-0004-01 Zhejiang 237 ml — — FDA listed —
H2One 75 mL/100mLthis 75742-0006-01 Zhejiang 237 ml — — FDA listed —
Healing Solutions 75 mL/100mL 75742-0007-01 Zhejiang 237 ml — — FDA listed —
Hand Sanitizer Alcohol Hand .75 mL/mL 76892-0001-01 Design 1000 ml — — FDA listed —
Instant Free Hand Sanitizer .75 mL/mL 77129-0000-50 Travel 50 ml — — FDA listed —
Hand Sanitizer .75 mL/mL 77129-0001-50 Travel 50 ml — — FDA listed —
Parasol Scent-Free Hand Sanitizer .75 mL/mL 77446-0001-00 We've 500 ml — — FDA listed —
Anti Bacterial Hand Sanitizer .75 mL/mL 78713-0000-02 MiWorld 60 ml — — FDA listed —
Hand Sanitizer .75 mL/mL 79401-0001-01 ORR 60 ml — — FDA listed —
Instant HAND SANITIZER .75 mL/mL 79524-0000-02 Xact 60 ml — — FDA listed —
Hand Sanitizer .75 mL/mL 79631-0000-00 Andaz 35 ml — — FDA listed —
hand sanitizer .75 mL/mL 80689-0000-00 Hygieia 30 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 75 mL/100mL 83807-0001-01 EVERLIT 9 ml — — FDA listed —
Hand Sanitizer 75 g/100mL 87111-0001-01 Zhejiang 30 ml — — FDA listed —
Green Island 75 mL/100mL 75742-0002-01 Zhejiang 30 ml — — FDA listed —
MyMedic Super Sanitizer 75 mL/100mL 43473-0307-01 Nantong 1.01 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.

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.

💡 Tap an ingredient (hover on desktop) to see what it is and why it’s used.

  • UNII H4N855PNZ1
    Alpha-tocopherol is a form of vitamin E, a fat-soluble antioxidant derived from natural or synthetic sources. In medicines, it prevents oils and fats from breaking down and becoming rancid, protecting the product's stability and shelf life.
  • UNII ZY81Z83H0X
    Aloe vera leaf is a plant extract derived from the aloe plant. It is used in medicines as a natural moisturizer and skin-soothing agent in topical formulations.
  • UNII 0A5MM307FC
    A synthetic polymer that absorbs water and forms a thick, gel-like substance. In medicines, it works as a thickener and stabilizer to improve texture and help ingredients stay mixed together in creams, gels, and lotions.
  • UNII PDC6A3C0OX
    Glycerin is a clear, thick liquid derived from plant oils or fats. It acts as a humectant to retain moisture, a sweetener, and a solvent in medications.
  • UNII 9O3K93S3TK
    Trolamine is an alkaline compound used as a pH buffer and emulsifier in medicines. It helps neutralize acids, stabilize formulations, and enable mixing of oil and water-based ingredients.
  • UNII 059QF0KO0R
    Water is a liquid solvent that dissolves and mixes ingredients together in liquid medicines, syrups, and injections. It helps distribute the active drug evenly throughout the product.

6 inactive ingredients listed in the exact product block matched to this NDC.

The official label also statesAqua Glycerin Carbomer Aloe Vera Triethanolamine Vitamin E

Label-section wording can be broader than the structured product block and may mention additional formulation ingredients.

Where does this data come from?
Data sourced from official FDA Structured Product Labeling (SPL) via DailyMed — ingredient classCode="IACT" elements from the exact product block matched by this NDC. Label-section narrative from DailyMed / the openFDA label index is shown separately when available.

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

LabelerZhejiang Guoyao Jingyue Aerosol Co., Ltd.
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code75742
First marketedJul 2020
Product typeHuman Otc Drug
Portfolio92 products on file

More NDCs from Zhejiang Guoyao Jingyue Aerosol Co., Ltd. labeler code 75742

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 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 8 words ▾

Uses To help reduce bacteria on the skin

⏱️ Dosage and Administration 31 words ▾

Directions Place enough product in your palm to thoroughly cover your hands. Rub hands together briskly until dry. Children under 6 years of age should be supervised when using this product.

⚠️ Warnings 63 words ▾

Warnings For external use only Avoid contact with eyes. If contact occurs, rinse thoroughly with water. FLAMMABLE, KEEP AWAY FROM FIRE Stop Use and Ask a Doctor Stop use and ask a doctor if rash or irritation or redness develops and lasts. Keep out of reach of children If product is swallowed, get medical help or contact a Poison Control Center right away.

📦 Storage and Handling 11 words ▾

Other information Store below 110F(43C) May discolor certain fabrics or surfaces

🧪 Active Ingredient 5 words ▾

Active Ingredient Ethyl Alcohol 75%

🧪 Inactive Ingredients 10 words ▾

Inactive Ingredients Aqua Glycerin Carbomer Aloe Vera Triethanolamine Vitamin E

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Stop Use and Ask a Doctor If 21 words ▾

Stop Use and Ask a Doctor Stop use and ask a doctor if rash or irritation or redness develops and lasts.

📄 Keep Out of Reach of Children 21 words ▾

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

📄 Package Label / Principal Display Panel 2 words ▾

label Label

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 H2One (this brand).

Top reported reactions

Drug Abuse48
Toxicity To Various Agents31
Overdose27
Intentional Overdose19
Poisoning Deliberate19
Suicide Attempt19
Completed Suicide18

Age at onset

Adolescent2
Adult30
Elderly5

Reporter sex

236 reports
Male · 61%
Female · 39%

Serious outcomes

Hospitalization99
Death74
Life-threatening10
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 23 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 ✓ Available
Inactive ingredients (structured) ✓ 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 Zhejiang Guoyao Jingyue Aerosol Co., Ltd.. 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 4 other package presentations of this same product, including 250 ml (75742-0006-03), 375 ml (75742-0006-02), 500 ml (75742-0006-04). 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?
Zhejiang Guoyao Jingyue Aerosol Co., Ltd. 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.
← 75742-0005-01 · Zhejiang 75742-0007-01 · Zhejiang →
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.