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Genuine First Aid Antiseptic Hand Sanitizer Ethyl Alcohol .62 mL/mL Cream, 1.03 mL — NDC 50814-0056-01 package photo

Genuine First Aid Antiseptic Hand Sanitizer Ethyl Alcohol .62 mL/mL Cream, 1.03 mL

by GFA Production (Xiamen) Co., Ltd. · 1.03 mL in 1 PACKAGE (50814-056-01)
NDC 50814-0056-01
🏷️ FDA NDC (as labeled) 50814-056-01 billing pads the product segment with a zero
OTC On market Non-controlled
🗂️ 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 →

This page is curated, coded, and maintained by

Compiled from public FDA, CMS, DailyMed, NADAC, and related drug data sources. Editorial policy

🆔 Identity & classification

FDA NDC (as labeled) 50814-056-01
Product NDC 50814-056
11-digit billing NDC 50814005601
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID af08c1f3-b1c4-58aa-e053-2a95a90ab320
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2020-01-01
Route TOPICAL
Dosage form CREAM
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 50814-056-01 — 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 → 50814-0056-01. 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.

🏭 Manufacturer & labeler

LabelerGFA Production (Xiamen) Co., Ltd.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code50814
First marketedJan 2020
Product typeHuman Otc Drug
Portfolio25 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?
📖 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.

🧪 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 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
candy cutie hand sanitizer .62 mL/mL 11673-0074-00 Target 30 ml — — FDA listed —
cheerful choco orange hand sanitizer .62 mL/mL 11673-0075-00 Target 30 ml — — FDA listed —
creamy cappuccino hand sanitizer .62 mL/mL 11673-0076-00 Target 30 ml — — FDA listed —
berry blitz hand sanitizer .62 mL/mL 11673-0078-00 Target 30 ml — — FDA listed —
choco mallow melt hand sanitizer .62 mL/mL 11673-0079-00 Target 30 ml — — FDA listed —
Coconut Macaroon Hand Sanitizer .62 mL/mL 11673-0780-00 Target 30 ml — — FDA listed —
Peppermint Twist Hand Sanitizer .62 mL/mL 11673-0781-00 Target 30 ml — — FDA listed —
Sparkling Cranberry Hand Sanitizer .62 mL/mL 11673-0782-00 Target 30 ml — — FDA listed —
Sugared Lemon Hand Sanitizer .62 mL/mL 11673-0783-00 Target 30 ml — — FDA listed —
Vanilla Sugar Cookie Hand Sanitizer .62 mL/mL 11673-0784-00 Target 30 ml — — FDA listed —
berries and cream hand sanitizer .62 mL/mL 11673-0785-00 Target 30 ml — — FDA listed —
Justice 194011 Heart It Antibac Blackberry And Vanilla Scented Anti-Bacterial Hand Sanitizer .62 mL/mL 60637-0240-00 Tween 30 ml — — FDA listed —
Justice 198824 You Rock Antibacterial Cotton Candy Blueberry Hand Sanitizer .62 mL/mL 60637-0302-30 Tween 30 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 61805-0110-01 Bath 50 ml — — FDA listed —
DawnMist Alcohol Hand Sanitizer .62 mL/mL 65517-1023-01 Dukal 118 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 70412-0191-08 Zhejiang 236 ml — — FDA listed —
Antibacterial Hand Sanitizer .62 mL/mL 73796-0110-15 Prostock 15 ml — — FDA listed —
Antibacterial Hand Sanitizer .62 mL/mL 73796-0111-20 Prostock 120 ml — — FDA listed —
Antibacterial Hand Sanitizer .62 mL/mL 73796-0112-36 Prostock 236 ml — — FDA listed —
Antibacterial Hand Sanitizer .62 mL/mL 73796-0114-73 Prostock 473 ml — — FDA listed —
Lavender Hand Sanitizer Girl .62 mL/mL 74177-0003-30 K7 30 ml — — FDA listed —
Peppermint Hand Sanitizer Girl .62 mL/mL 74177-0004-30 K7 30 ml — — FDA listed —
Watermelon Hand Sanitizer Girl .62 mL/mL 74177-0005-30 K7 30 ml — — FDA listed —
Cherry Hand Sanitizer Boy .62 mL/mL 74177-0006-30 K7 30 ml — — FDA listed —
Lemonade Hand Sanitizer Boy .62 mL/mL 74177-0007-30 K7 30 ml — — FDA listed —
PEPPERMINT HAND SANITIZER boy .62 mL/mL 74177-0010-30 K7 30 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 74177-0021-00 K7 236 ml — — FDA listed —
Hibiscus ROSE HAND SANITIZER .62 mL/mL 74177-0024-00 K7 236 ml — — FDA listed —
Lavender ALOE HAND SANITIZER .62 mL/mL 74177-0025-00 K7 236 ml — — FDA listed —
Natural ALOE HAND SANITIZER .62 mL/mL 74177-0026-00 K7 236 ml — — FDA listed —
berry blast scent hand sanitizer .62 mL/mL 74177-0031-00 K7 30 ml — — FDA listed —
bubble gum scent hand sanitizer .62 mL/mL 74177-0032-00 K7 30 ml — — FDA listed —
citrus crush scent hand sanitizer panda .62 mL/mL 74177-0033-00 K7 30 ml — — FDA listed —
citrus crush scent hand sanitizer robot .62 mL/mL 74177-0034-00 K7 30 ml — — FDA listed —
lemon lime scent hand sanitizer .62 mL/mL 74177-0035-00 K7 30 ml — — FDA listed —
vanilla frosting scent hand sanitizer .62 mL/mL 74177-0036-00 K7 30 ml — — FDA listed —
Slight Scent Hand Sanitizer .62 mL/mL 74641-0000-01 Sobe 15 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 74712-0000-01 In 50 ml — — FDA listed —
Parasol Hand Sanitizer .62 mL/mL 77446-0000-50 We've 50 ml — — FDA listed —
FINEAPPLE Hand Sanitizer .62 mL/mL 78768-0002-30 CROP 30 ml — — FDA listed —
MELON DOLLAR Hand Sanitizer .62 mL/mL 78768-0003-30 CROP 30 ml — — FDA listed —
knDR SANITIZER .62 mL/mL 78768-0004-30 CROP 30 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 80524-0000-15 Tempo 15 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 80524-0001-20 Tempo 20 ml — — FDA listed —
Genuine First Aid Antiseptic Hand Sanitizer Ethyl Alcohol .62 mL/mLthis 50814-0056-01 GFA 1.03 ml — — FDA listed —
Hand Sanitizer .62 mL/mL 66715-7012-08 Lil' 1 bottle — — 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
Jan 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
50814-0056-01 You're viewing this 1.03 mL in 1 PACKAGE (50814-056-01) 2020-01-01 Active

🧭 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 FDA registers it as 50814-056-01, 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: 50814-0056-01, written without dashes as 50814005601. 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 50814-0056-01, the first segment (50814) is the labeler code FDA assigned to GFA Production (Xiamen) Co., Ltd.; the middle segment (0056) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (01) identifies this exact package size and type. Together they name one specific package of one specific product.
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 GFA Production (Xiamen) Co., Ltd.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
GFA Production (Xiamen) 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.

📄 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 13 words ▾

Uses For handwashing to decrease bacteria on the skin Recommended for repeated use.

⏱️ Dosage and Administration 12 words ▾

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

⚠️ Warnings 55 words ▾

Warnings Flammable, keep away from fire or flame For external use only. Do not use in the eyes. Stop use and ask a doctor if irritation and redness develop. condition persists for more than 72 hours Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

🧪 Active Ingredient 8 words ▾

Active ingredient Ethyl alcohol, 62% v/v Purpose Antiseptic

🧪 Inactive Ingredients 9 words ▾

Inactive ingredients Carbomer, propylene glycol, purified water, titanium dioxide

🎯 Purpose 2 words ▾

Purpose Antiseptic

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 50814-0055-01 · GFA 50814-0057-01 · GFA →
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.