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ANTIBACTERIAL HAND SANITIZER ETHYL ALCOHOL 70 mL/100mL Gel, 8 mL — NDC 73145-009-01 (Billing 73145-0009-01)

by ASC Marketing Ltd. · 8 mL in 1 BOTTLE, SPRAY

This is a package of 8 mL of ANTIBACTERIAL HAND SANITIZER ETHYL ALCOHOL 70 mL/100mL Gel from ASC Marketing Ltd., marketed since Nov 2020 and currently FDA-listed. It is this product's only package size.

NDC 73145-0009-01
🏷️ FDA NDC (as labeled) 73145-009-01 billing pads the product segment with a zero
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

⚠️
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) 73145-009-01
Product NDC 73145-009
11-digit billing NDC 73145000901
UNII 3K9958V90M
Application # M005
SPL Set ID b42ebe64-0cad-2d26-e053-2a95a90af3dd
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-11-16
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 73145-009-01 — 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 → 73145-0009-01. 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.

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.
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
73145-0009-01 You're viewing this Main listing 8 mL in 1 BOTTLE, SPRAY 2020-11-16 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Hand sanitizer 1.8oz with extra clip original 70 mL/100mL 57337-0147-01 Rejoice 53 ml — — FDA listed —
Hand sanitizer 2oz 2pk original 70 mL/100mL 57337-0148-01 Rejoice 59 ml — — FDA listed —
Hand sanitizer 1.8oz with extra clip original 70 mL/100mL 75742-0026-01 Zhejiang 53 ml — — FDA listed —
Hand sanitizer 2oz 2pk original 70 mL/100mL 75742-0027-01 Zhejiang 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 80335-0103-02 EverywhereAire 60 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Strawberry 70 mL/100mL 75742-0036-01 Zhejiang 53 ml — — FDA listed —
Advanced Hand Sanitizer with Aloe 70 mL/100mL 83986-0996-32 UpLift 355 ml — — FDA listed —
24 7 life by 7 Eleven Instant Hand Sanitizer 70 mL/100mL 10202-0400-01 7-ELEVEN, 59 ml — — FDA listed —
Instant Hand Sanitizer 70 mL/100mL 57337-0085-02 Rejoice 3 bottles — — FDA listed —
Caseys Antimicrobial Hand Sanitizer 70 mL/100mL 67751-0071-01 Navajo 59 ml — — FDA listed —
American Red Cross 70% Ethyl Alcohol Hand Sanitizer 70 mL/100mL 75742-0018-01 Zhejiang 236 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Fresh Citrus 70 mL/100mL 75742-0033-01 Zhejiang 53 ml — — FDA listed —
Quality Choice Instant Hand Sanitizer 70 mL/100mL 77725-0004-08 L.e.d. 236 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 79903-0334-03 Walmart 89 ml — — FDA listed —
Sanitizing Hand Gel Unscented 70 mL/100mL 82355-0020-08 ALO 238 ml — — FDA listed —
Advanced 70 mL/100mL 36800-0370-16 Topco 59 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Strawberry 70 mL/100mL 51628-4438-01 MY 53 ml — — FDA listed —
Epi-Clenz Pure Instant Hand Antiseptic 70 mL/100mL 53329-0203-04 Medline 118 ml — — FDA listed —
Spa Hand Sanitizer Vanilla 70 mL/100mL 57337-0187-01 Rejoice 236 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 63941-0439-34 Valu 236 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 72036-0439-16 Harris 59 ml — — Discontinued —
Sweet Orange Bergamot and Aloe 70 mL/100mL 82355-0002-08 ALO 238 ml — — FDA listed —
Sanitizing Hand Gel Peppermint Eucalyptus 70 mL/100mL 82355-0021-08 ALO 238 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 36800-0898-16 Topco 59 ml — — FDA listed —
Tork Hand Sanitizer Alcohol Gel 70 mL/100mL 49351-0105-01 Essity 1000 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Lavender 70 mL/100mL 51628-4436-01 MY 53 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 59779-0070-16 CVS 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 83986-0529-16 UpLift 59 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 72288-0435-16 Amazon.Com 59 ml — — FDA listed —
Sanitizing Hand Gel Lemongrass 70 mL/100mL 82355-0022-08 ALO 238 ml — — FDA listed —
American Red Cross 70% Ethyl Alcohol Hand Sanitizer 70 mL/100mL 51628-4434-01 MY 236 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Original 70 mL/100mL 51628-4437-01 MY 53 ml — — FDA listed —
Medline 70 mL/100mL 53329-0230-02 Medline 2.4 ml — — FDA listed —
Advanced 70 mL/100mL 75981-0370-16 Perrigo 59 ml — — FDA listed —
Cupcake Scent Hand Sanitizer 70 mL/100mL 87302-0217-17 Amber 30 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 30142-0596-16 The 59 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Fresh Citrus 70 mL/100mL 51628-4435-01 MY 53 ml — — FDA listed —
Spectrum Hand Sanitizer Wipes 70 mL/100mL 53329-0840-32 Medline 20 applicators — — FDA listed —
Spa Hand Sanitizer Champagne Blash 70 mL/100mL 57337-0188-01 Rejoice 236 ml — — FDA listed —
Spa Hand Sanitizer Summer Lemon 70 mL/100mL 57337-0189-01 Rejoice 236 ml — — FDA listed —
Vanilla Scent Hand Sanitizer 70 mL/100mL 87302-0214-14 Amber 30 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 53863-0002-01 Exelencia 50 ml — — FDA listed —
Spa Hand Sanitizer Wrter Melon Splash 70 mL/100mL 57337-0190-01 Rejoice 236 ml — — FDA listed —
Hand Essentials Instant Hand Antiseptic 70 mL/100mL 65626-0206-04 Hu-Friedy 118 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 67623-0002-01 Biocosmetica 50 ml — — FDA listed —
American Red Cross 70% Ethyl Alcohol Hand Sanitizer 70 mL/100mL 75742-0032-01 Zhejiang 236 ml — — FDA listed —
Caring Mill Triple Hand Sanitizer with Lavender 70 mL/100mL 81522-0900-01 FSA 354 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 41250-0370-06 Meijer, 33 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 53329-0202-04 Medline 118 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 53942-0439-16 Demoulas 59 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 72476-0439-16 Retail 59 ml — — FDA listed —
Pfa 70 mL/100mL 75742-0008-01 Zhejiang 2 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Lavender 70 mL/100mL 75742-0034-01 Zhejiang 53 ml — — FDA listed —
Amoray 70% Ethyl Alcohol Hand Sanitizer Original 70 mL/100mL 75742-0035-01 Zhejiang 53 ml — — FDA listed —
Strawberry Scent Hand Sanitizer 70 mL/100mL 87302-0216-16 Amber 30 ml — — FDA listed —
Advanced 70 mL/100mL 72288-0370-45 Amazon.Com 946 ml — — FDA listed —
Antibacterial Hand Sanitizer 70 mL/100mLthis 73145-0009-01 ASC 8 ml — — FDA listed —
Quality Choice Instant Hand Sanitizer 70 mL/100mL 77725-0003-02 L.e.d. 59 ml — — FDA listed —
Palma Hand Sanitizer 70 mL/100mL 81286-0101-10 UNITRADE 1 bottle — — Discontinued —
Hand Sanitizing Wipes 70 mL/100mL 83986-0028-64 UpLift 20 packets — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 83986-0439-16 UpLift 59 ml — — FDA listed —
Watermelon Scent Hand Sanitizer 70 mL/100mL 87302-0215-15 Amber 30 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 11673-0439-16 Target 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 69790-0770-16 Uline 59 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
Nov 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.

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

LabelerASC Marketing Ltd.
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code73145
First marketedNov 2020
Product typeHuman Otc Drug
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 9 words ▾

Uses For handwashing to decrease bacteria on the skin.

⏱️ Dosage and Administration 13 words ▾

Directions Wet hands thoroughly for with product and allow to dry without wiping.

⚠️ Warnings 43 words ▾

Warnings Flammable. Keep away from fire and flame. For external use only. Do not use in eyes. In case of contact，rinse eyes thoroughly with water. Discontinue use if irritation or redness develop. If condition persists for more than 72 hours consult a doctor.

🧪 Active Ingredient 5 words ▾

Active ingredient Ethyl alcohol 70%

🧪 Inactive Ingredients 12 words ▾

Inactive Ingredients Water, Glycerin, Propylene Glycol, Fragrance, Aloe Barbadensis Leaf Juice, Maltodextrin.

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel 4 words ▾

image of bottle 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 Antibacterial Hand Sanitizer (this brand).

Top reported reactions

Toxicity To Various Agents6,035
Completed Suicide5,451
Drug Abuse5,333
Overdose1,915
Death1,601
Intentional Overdose1,559
Suicide Attempt1,359

Reporter sex

26,956 reports
Male · 55%
Female · 45%
Unknown · 0%

Serious outcomes

Death15,202
Life-threatening1,413
Disabling212
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,671 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 ASC Marketing Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
ASC Marketing 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.
← 73145-0007-01 · ASC 73145-0010-01 · ASC →
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.