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Ethanol Alcohol 70 mL/100mL Gel, 59 mL — NDC 82442-0031-02 package photo

Ethanol Alcohol 70 mL/100mL Gel, 59 mL

by TARGET CORPORATION INC. · 59 mL in 1 BOTTLE, PLASTIC (82442-031-02)
NDC 82442-0031-02
🏷️ FDA NDC (as labeled) 82442-031-02 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) 82442-031-02
Product NDC 82442-031
11-digit billing NDC 82442003102
UNII 3K9958V90M
UPC 0191907963885
Application # 505G(a)(3)
SPL Set ID 28ef35a8-e6ca-9669-e063-6394a90abf8f
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2025-03-01
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 82442-031-02 — 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 → 82442-0031-02. 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

LabelerTARGET CORPORATION INC.
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code82442
First marketedMar 2025
Product typeHuman Otc Drug
Portfolio11 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.

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

  • UNII A7E6112E4N
    A form of vitamin E used as an antioxidant in medicines. It prevents oils and fats in the product from breaking down, helping maintain stability and shelf life.
  • UNII RUE8E6T4NB
    Aloe vera leaf juice is a clear gel extracted from aloe vera plant leaves. It's used in medicines as a lubricant, emollient, and preservative to soothe skin contact and help keep the product stable.
  • UNII 329LCV5BTF
    A blend of fragrance compounds used to add pleasant smell to the medicine. Fragrances mask bitter or unpleasant tastes and odors, making the medication easier to take.
  • 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 ND2M416302
    Isopropyl alcohol is a clear liquid solvent derived from petroleum. In medicines, it dissolves active ingredients and other components, helps the product flow smoothly, and aids in sterilization during manufacturing.
  • UNII 0RE8K4LNJS
    Isopropyl myristate is an oily liquid made from coconut or palm oil. It's used in medicines as an emollient and penetration enhancer to help the medicine absorb through skin or improve spreadability in topical products.
  • 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.

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

The official label also statesAloe Barbadensis Leaf Juice, Fragrance (Parfum), Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Tocopheryl Acetate, Water (Aqua).

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.

💲 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
AntiochPharma Hand Sanitizer 70 mL/100mL 11383-0308-09 Weeks 259 ml — — FDA listed —
AntiochPharma Rapidgel Hand Sanitizer 70 mL/100mL 11383-0309-02 Weeks 59 ml — — FDA listed —
Brompton and Langley Moisturizing Hand Sanitizer Lavnder Vanilla 70 mL/100mL 56136-0730-01 Ganzhou 15 ml — — FDA listed —
AZX Wellness Hand Sanitizer 70 mL/100mL 73145-0012-01 ASC 2 ml — — FDA listed —
Alcohol Antiseptic Hand Sanitizer 70 mL/100mL 74876-0656-08 Custom 237 ml — — FDA listed —
Alcohol Antiseptic Hand Sanitizer Antibacterial 70 mL/100mL 75742-0028-01 Zhejiang 237 ml — — FDA listed —
Hand Sanitizer gel 70 mL/100mL 80335-0114-02 EverywhereAire 60 ml — — FDA listed —
Coconut and Lime Scented Hand Sanitizer 70 mL/100mL 80684-0030-01 FOURSTAR 1 bottle — — FDA listed —
Cucumber and Melon Scented Hand Sanitizer 70 mL/100mL 80684-0031-01 FOURSTAR 1 bottle — — FDA listed —
Pomegranate and Vanilla Scented Hand Sanitizer 70 mL/100mL 80684-0032-01 FOURSTAR 1 bottle — — FDA listed —
Lavender scented anti-bacterial hand sanitizer 70 mL/100mL 80684-0033-01 FOURSTAR 59 ml — — FDA listed —
Aloe scented anti-bacterial hand sanitizer 70 mL/100mL 80684-0034-01 FOURSTAR 59 ml — — FDA listed —
Rose scented anti-bacterial hand sanitizer 70 mL/100mL 80684-0035-01 FOURSTAR 59 ml — — FDA listed —
Jasmine scented anti-bacterial hand sanitizer 70 mL/100mL 80684-0036-01 FOURSTAR 59 ml — — FDA listed —
Berry Scented Clip On Hand Sanitizer 70 mL/100mL 80684-0060-02 Fourstar 59 ml — — FDA listed —
Cherry Blossom Scented Hand Sanitizer 70 mL/100mL 80684-0061-08 Fourstar 236 ml — — FDA listed —
Chai Latte Scented Clip On Hand Sanitizer 70 mL/100mL 80684-0062-02 Fourstar 59 ml — — FDA listed —
Chai Latte Scented Hand Sanitizer 70 mL/100mL 80684-0063-02 Fourstar 59 ml — — FDA listed —
Pumpkin Spice Scented Clip On Hand Sanitizer 70 mL/100mL 80684-0064-02 Fourstar 59 ml — — FDA listed —
Pumpkin Spice Scented Hand Sanitizer 70 mL/100mL 80684-0065-02 Fourstar 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 79903-0335-12 Walmart 355 ml — — FDA listed —
Perk Hand Sanitizer Moisturizing Gel 70 mL/100mL 80434-0280-08 Worklifebrands 236 ml — — FDA listed —
XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E and Aloe 70 mL/100mL 87559-0001-01 Rejoice 1 bottle — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Sunshine and Lemons 70 mL/100mL 62670-6679-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Snowy Peach Berry 70 mL/100mL 62670-6741-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Afternoon Apple Picking 70 mL/100mL 62670-6891-00 Bath 29 ml — — FDA listed —
Thick Hand Sanitizer 70 mL/100mL 68400-0487-01 Mycone 3780 ml — — FDA listed —
Hand Recovery 70 mL/100mL 70741-0007-06 Derma 947.2 ml — — FDA listed —
On Guard Sanitizing Gel 70 mL/100mL 71630-0098-50 doTERRA 50 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer 70 mL/100mL 74149-0103-01 Yiwu 236 ml — — FDA listed —
Singular Wipes 70 mL/100mL 81428-0070-04 SINGULAR 4 ml — — FDA listed —
Scriptsusa Hand Sanitizer 70 mL/100mL 87474-0001-07 Energized 177 ml — — FDA listed —
Instaclean Hand Sanitizing 70 mL/100mL 52410-8046-02 SHIELD 118 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 59779-0059-16 CVS 59 ml — — Discontinued —
Anti Bacterial Moisturizing Hand Sanitizer Champagne Toast 70 mL/100mL 62670-6731-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Pomegranate and Blackberry 70 mL/100mL 62670-6857-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Winter Citrus Wreath 70 mL/100mL 62670-6954-00 Bath 29 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Calming Lavender 70 mL/100mL 21749-0127-02 GOJO 59 ml — — FDA listed —
PURELL Advanced Hand Sanitizer Energizing Mint 70 mL/100mL 21749-0128-02 GOJO 59 ml — — FDA listed —
Purell Advanced Moisturizing 2in1 70 mL/100mL 21749-0751-04 GOJO 118 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 57243-0370-16 Salado 59 ml — — FDA listed —
Ethyl Alcohol 70 mL/100mL 59448-0011-01 ASP 53 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Tis The Season 70 mL/100mL 62670-6739-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Fresh Coconut and Cotton 70 mL/100mL 62670-6783-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Beautiful Day 70 mL/100mL 62670-6852-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Lavender Bergamot 70 mL/100mL 62670-6975-00 Bath 29 ml — — FDA listed —
Guard 70 mL/100mL 63148-0502-08 Apollo 227 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 67091-0107-02 WinCo 59 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer with Aloe 70 mL/100mL 74149-0104-01 Yiwu 473 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer 70 mL/100mL 74149-0105-01 Yiwu 473 ml — — FDA listed —
Travel Wipes Moisturizer and fragrance 70 mL/100mL 81428-0074-01 SINGULAR 15 pouches — — FDA listed —
Hand Sanitizer 70 mL/100mL 83986-0456-04 UpLift 750 ml — — FDA listed —
Instant Hand Sanitizer 70 mL/100mL 10565-0076-02 Hydrox 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 11344-0370-16 Nice-Pak 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 53942-0370-16 Demoulas 59 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Gingerbread Bakery 70 mL/100mL 62670-6742-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Starfruit Sangria 70 mL/100mL 62670-6855-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Flannel 70 mL/100mL 62670-6971-00 Bath 29 ml — — FDA listed —
Purell 70 mL/100mL 67751-0188-01 Navajo 30 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer With Aloe 70 mL/100mL 74149-0107-01 Yiwu 59 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 77955-0003-03 Custom 500 ml — — FDA listed —
Ethanol 70 mL/100mLthis 82442-0031-02 TARGET 59 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 41190-0439-34 Wakefern 236 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Fresh Cut Lilacs 70 mL/100mL 62670-6851-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Blueberry Bellini 70 mL/100mL 62670-6854-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Sweet Cinnamon Pumpkin 70 mL/100mL 62670-6970-00 Bath 29 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 63868-0882-16 Chain 59 ml — — Discontinued —
CVS Hand Sanitizer 70 mL/100mL 69842-0760-02 CVS 59 ml — — FDA listed —
Alcohol 70 mL/100mL 82442-0003-02 TARGET 59 ml — — FDA listed —
Moxe Citrus Splash Hand Sanitizer 70 mL/100mL 84004-0001-32 Premark 946 ml — — FDA listed —
XtraCare Hand Sanitizer Antibacterial Moisturize with Vitamin E 70 mL/100mL 87559-0000-01 Rejoice 1 bottle — — FDA listed —
Instant Hand Sanitizer Unscented 70 mL/100mL 10565-0075-02 Hydrox 59 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 11822-3700-01 Rite 59 ml — — FDA listed —
Purell Advanced Refreshing 70 mL/100mL 21749-0704-01 GOJO 29 ml — — FDA listed —
Summit 375 Gel Alcohol Hand Sanitizer 70 mL/100mL 23590-0400-10 R.L. 850 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 56062-0370-16 Publix 59 ml — — FDA listed —
Instant Hand Sanitizer 70 mL/100mL 61598-0450-04 LTC 118 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Gel Leaves 70 mL/100mL 62670-6675-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Mahogany Teakwood 70 mL/100mL 62670-6678-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Tree Farm 70 mL/100mL 62670-6743-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Iced Lemon Pound Cake 70 mL/100mL 62670-6853-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer White T-Shirt 70 mL/100mL 62670-6973-00 Bath 29 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 63941-0008-16 Valu 59 ml — — FDA listed —
Instant Hand Sanitizer Unscented 70 mL/100mL 65626-0470-16 Hu-Friedy 473 ml — — FDA listed —
Avant 70% Alcohol Gel 70 mL/100mL 68306-0116-01 B4 208198 ml — — FDA listed —
Optimize Thick Hand Sanitizer 70 mL/100mL 68400-0486-06 Mycone 177.4 ml — — Discontinued —
Hand Sanitizer 70 mL/100mL 72476-0370-34 Retail 236 ml — — FDA listed —
Signature Care Advanced Hand Sanitizer with Aloe 70 mL/100mL 74149-0102-01 Yiwu 236 ml — — FDA listed —
Advanced Hand Sanitizer 70 mL/100mL 41190-0370-16 Wakefern 59 ml — — Discontinued —
Anti Bacterial Moisturizing Hand Sanitizer Fresh Sparkling Snow 70 mL/100mL 62670-6740-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Rose Water and Ivy 70 mL/100mL 62670-6856-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Gingerbread Bakery 70 mL/100mL 62670-6909-00 Bath 29 ml — — FDA listed —
Anti Bacterial Moisturizing Hand Sanitizer Beautiful Day 70 mL/100mL 62670-6974-00 Bath 29 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 63148-0632-02 Apollo 59 ml — — FDA listed —
Instant Hand Sanitizer Citrus 70 mL/100mL 75115-0467-02 Soapbox 59 ml — — FDA listed —
Hand Sanitizer Wipes 70 mL/100mL 75214-0501-20 HANUL 134 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

🏛️
2025
On the market since
Mar 2025
📍
2026
Currently FDA-listed
1 year 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 Ethanol (this brand).

Top reported reactions

Completed Suicide8,226
Toxicity To Various Agents7,748
Drug Abuse6,914
Death2,725
Overdose2,301
Cardio-respiratory Arrest2,150
Intentional Overdose1,936

Reporter sex

34,670 reports

Serious outcomes

Hospitalization9,605
Life-threatening1,586
Disabling227
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 2,567 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.

📦 Packaging — all sizes for this product

Package NDCDescription Marketing startStatus
82442-0031-02 You're viewing this 59 mL in 1 BOTTLE, PLASTIC (82442-031-02) 2025-03-01 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) ✓ 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 82442-031-02, 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: 82442-0031-02, written without dashes as 82442003102. 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 82442-0031-02, the first segment (82442) is the labeler code FDA assigned to TARGET CORPORATION INC.; the middle segment (0031) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (02) 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 TARGET CORPORATION INC.. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
TARGET CORPORATION 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 28 words ▾

Uses For personal hand hygiene to help prevent the spread of bacteria, and can be used in place of hand washing if soap and water are not available.

⏱️ Dosage and Administration 29 words ▾

Directions For occassional and personal use. Rub thoroughly into hands for at least 30 seconds. Allow to dry. Children under 6 should only use the product under adult supervision.

⚠️ Warnings 69 words ▾

Warnings For External use only. Flammable. Keep away from source of heat or fire. When using this product Avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water. Do not inhale or ingest. Stop use and ask a doctor if irritation or redness develops and lasts. Keep out of reach of children In case of accidental ingestion, get medical help or contact a Poison Control Center immediately.

🧪 Active Ingredient 5 words ▾

Active Ingredient Ethyl Alcohol 70%

🧪 Inactive Ingredients 17 words ▾

Inactive Ingredients Aloe Barbadensis Leaf Juice, Fragrance (Parfum), Glycerin, Isopropyl Alcohol, Isopropyl Myristate, Tocopheryl Acetate, Water (Aqua).

🎯 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 ↗
← 82442-0029-02 · Target 82442-0060-12 · Target →
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.