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BLUESEA DISPOSABLE HAND SANITIZER Alcohol 75 mL/100mL Solution, 237 mL — NDC 72119-0002-03 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

BLUESEA DISPOSABLE HAND SANITIZER Alcohol 75 mL/100mL Solution, 237 mL — NDC 72119-002-03 (Billing 72119-0002-03)

by BLUE SEA AEROSOL & DAILY CARE CO., LTD · 237 mL in 1 BOTTLE

This is a package of 237 mL of BLUESEA DISPOSABLE HAND SANITIZER Alcohol 75 mL/100mL Solution from BLUE SEA AEROSOL & DAILY CARE CO., LTD, marketed since Jun 2020 and currently FDA-listed.

NDC 72119-0002-03
🏷️ FDA NDC (as labeled) 72119-002-03 billing pads the product segment with a zero
This package
Contains237 mL Pack sizes5 compare ↓
Product page 72119-0002-01 Also comes in: 60 ml 72119-002-01 100 ml 72119-002-02 300 ml 72119-002-04 500 ml 72119-002-05
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

NDC database record

One package, one record: these facts belong to NDC 72119-002-03 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
72119 labeler · 002 product · 03 package
Package marketed since
Jun 8, 2020
Sample package
No — commercial package
Listing certified through
Dec 31, 2026
Barcode (UPC-A, from the NDC)
3 7211900203 0
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 72119-002-03
Product NDC 72119-002
11-digit billing NDC 72119000203
RxCUI 1047755
UNII 3K9958V90M
Application # M005
SPL Set ID 7a552be2-a9e1-4c6f-b1c2-79113a73bd2f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-06-08
Route TOPICAL
Dosage form SOLUTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1047755
Why two NDCs? The FDA registers this code as 72119-002-03 — 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 → 72119-0002-03. 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 mLPer 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: 60 ml 100 ml 300 ml 500 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
72119-0002-01 72119-002-01 Main listing 60 mL in 1 BOTTLE 2020-06-08 — Active
72119-0002-02 72119-002-02 100 mL in 1 BOTTLE 2020-06-08 — Active
72119-0002-03 You're viewing this 237 mL in 1 BOTTLE 2020-06-08 — Active
72119-0002-04 72119-002-04 300 mL in 1 BOTTLE 2020-06-08 — Active
72119-0002-05 72119-002-05 500 mL in 1 BOTTLE 2020-06-08 — Active

You're viewing one 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.
How does this package differ from NDC 72119-0002-01?
Both are BLUESEA DISPOSABLE HAND SANITIZER Alcohol 75 mL/100mL Solution — the drug itself is identical. This page's package is the 237 mL one, while NDC 72119-0002-01 is the 60 ml package.
What NDC number is used to bill for this package of BLUESEA DISPOSABLE HAND SANITIZER Alcohol 75 mL/100mL Solution?
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
75% Alcohol Disinfectant 75 mL/100mL 41366-0015-01 Zhejiang 88 ml — — FDA listed —
75% Alcohol Disinfectant 75 mL/100mL 41366-0016-01 Zhejiang 1000 ml — — FDA listed —
Bluesea Disposable Hand Sanitizer 75 mL/100mLthis 72119-0002-03 BLUE 237 ml — — FDA listed —
Hand Sanitizer 75 mL/100mL 73928-0002-01 KINGKEY 30 ml — — FDA listed —
Clean Simple Hand Sanitizer 75 mL/100mL 73928-0003-01 KINGKEY 60 ml — — FDA listed —
Anthem Hand Sanitizer 75 mL/100mL 73928-0007-01 KINGKEY 30 ml — — FDA listed —
ArmiCare Hand Sanitizer 75 mL/100mL 81793-0187-00 Armis 60 ml — — FDA listed —
Sipa hand sanitizer with Moisturizers 75 mL/100mL 83502-0002-01 Tourel 30 ml — — FDA listed —
MedBox Hand Sanitizer 75 mL/100mL 83638-0001-01 Harpers 20 bottles — — FDA listed —
Signature Series Enriched Foam Alcohol Hand Sanitizer 75 mL/100mL 42961-0017-01 Cintas 4 pouches — — FDA listed —
Mary Kay Satin Hands Shea Hand Sanitizer 75 mL/100mL 51531-8735-07 Mary 1 bottle — — FDA listed —
Hand Sanitizing Wipes 75 mL/100mL 84973-0075-01 Germs 176 ml — — FDA listed —
Hand Sanitizer 75 mL/100mL 64646-0420-12 Charlotte 575 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
Jun 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.

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

LabelerBLUE SEA AEROSOL & DAILY CARE CO., LTD
FDA applicationM005 (OTC MONOGRAPH DRUG)
Labeler code72119
First marketedJun 2020
Product typeHuman Otc Drug
Portfolio3 products on file

More NDCs from BLUE SEA AEROSOL & DAILY CARE CO., LTD labeler code 72119

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 📄 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 19 words ▾

Use To decrease bacteria on the skin that could cause disease Recommended for repeated use Use anywhere without water

⏱️ Dosage and Administration 25 words ▾

Directions Wet hands thoroughly with product and rub until dry without wiping For children under 6, use only under adult supervision Not recommended for infants

⚠️ Warnings 13 words ▾

Warnings For external use only -hands Flammable. Keep away from heat and flame

📦 Storage and Handling 17 words ▾

Other information Do not store above 105F May discolor some fabrics Harmful to wood finishes and plastics

🧪 Active Ingredient 6 words ▾

Active Ingredient(s) Ethyl Alcohol 75% v/v

🧪 Inactive Ingredients 6 words ▾

Inactive ingredients Water, glycerin, carbomer, triethanolamine

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 When Using This Product 28 words ▾

When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. Avoid contact with broken skin Do not inhale or ingest

📄 Stop Use and Ask a Doctor If 9 words ▾

Discontinue if skin becomes irritated and ask a doctor

📄 Keep Out of Reach of Children 22 words ▾

Keep out of reach of children. In case of accidental ingest, seek professional assistance or contact a Poison Control Center right away.

📄 Package Label / Principal Display Panel 2 words ▾

image description

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 BLUESEA DISPOSABLE HAND SANITIZER (this brand).

Top reported reactions

Toxicity To Various Agents6,004
Completed Suicide5,433
Drug Abuse5,289
Overdose1,888
Death1,594
Intentional Overdose1,540
Cardio-respiratory Arrest1,346

Age at onset

Neonate26
Infant14
Child16
Adolescent92
Adult2,810
Elderly294

Reporter sex

26,728 reports
Male · 55%
Female · 45%
Unknown · 0%

Serious outcomes

Death15,128
Hospitalization8,617
Life-threatening1,403
Disabling212
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,655 1,499
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) — 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 BLUE SEA AEROSOL & DAILY CARE 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 60 ml (72119-0002-01), 100 ml (72119-0002-02), 300 ml (72119-0002-04). 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?
BLUE SEA AEROSOL & DAILY CARE 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.
← 72113-0118-14 · Eden 72119-0003-01 · BLUE →
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.