HomeNDC LookupIngredientsEthyl Alcohol › 83986-0028-64
Hand Sanitizing Wipes Ethyl Alcohol 70 mL/100mL Cloth — NDC 83986-0028-64 package photo

Hand Sanitizing Wipes Ethyl Alcohol 70 mL/100mL Cloth

by UpLift Brands LLC · 20 PACKET in 1 POUCH (83986-028-64) / 3 mL in 1 PACKET
NDC 83986-0028-64
🏷️ FDA NDC (as labeled) 83986-028-64 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 →
⚠️
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

FDA NDC (as labeled) 83986-028-64
Product NDC 83986-028
11-digit billing NDC 83986002864
RxCUI 1489307
UNII 3K9958V90M
Application # 505G(a)(3)
SPL Set ID 044361fe-1e16-4fea-9094-a2d88c890d9c
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2023-11-21
Route TOPICAL
Dosage form CLOTH
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 83986-028-64 — 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 → 83986-0028-64. 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.

🏭 Manufacturer & labeler

LabelerUpLift Brands LLC
FDA application505G(a)(3) (OTC MONOGRAPH DRUG)
Labeler code83986
First marketedNov 2023
Product typeHuman Otc Drug
Portfolio8 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 →
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 9E8X80D2L0
    A synthetic form of vitamin E used as an antioxidant and preservative in medications. It helps prevent the active ingredients from degrading when exposed to oxygen or light.
  • 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 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 G7515SW10N
    A waxy liquid derived from vegetable oil and fatty acids. It works as an emulsifier and solubilizer to help blend oil and water-based ingredients together and improve how the medicine dissolves and is absorbed in the body.
  • 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.

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

The official label also stateswater, glycerin, glyceryl caprylate/caprate, Aloe barbadensis leaf juice, isopropyl myristate, tocopheryl acetate, fragrance

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 DailyMedingredient 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 eachPer 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
PDI Sani-Hands Instant Hand Sanitizing Wipes .7 mL/mL 10819-3916-01 Professional 100 packets FDA listed
PDI Sani Hands .7 mL/mL 10819-3918-01 Professional 20 applicators FDA listed
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6006-01 Professional 3.23 ml FDA listed
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6007-01 Professional 484 ml FDA listed
Sani Professional Hands Instant Sanitizing Wipes .7 mL/mL 10819-6008-01 Professional 805.44 ml FDA listed
Signature Select Instant Hand Sanitizer Wipes with Aloe Vera 70 mL/100mL 21130-0068-01 Living 24 patches FDA listed
Jianerkang Sanitizing Wipe .7 mL/mL 34645-0003-01 Jianerkang 1 patch FDA listed
Instant Hand Sanitizer STERILE 70 Ethyl Alcohol .7 mL/mL 34645-0007-01 Jianerkang 1 patch FDA listed
microdot Hand Sanitizing Wipe 70 mL/100mL 52422-0622-06 Cambridge 563.91 ml FDA listed
Spectrum Hand Sanitizer Wipes 70 mL/100mL 53329-0840-32 Medline 20 applicators FDA listed
Procure Products Hand Sanitizing Wipes 70 mL/100mL 55681-0135-02 TWIN 135 patches FDA listed
Total Solutions Hand Sanitizing Wipes 70 g/100g 62819-0448-00 Athea 70 applicators FDA listed
Soft Care Hand Sanitizing Wipes 70 g/100g 64536-1726-06 Diversey, 895 g FDA listed
Instant Hand Sanitizer Wipes 70 mL/100mL 64709-0185-10 Diamond 1 ml FDA listed
Zep Hand Sanitizer Wipes 70 mL 66949-0405-01 Zep 2 swabs FDA listed
Express Wipes Hand Sanitizer 7 g/10g 67858-0645-02 QuestSpecialty 6 canisters FDA listed
Alcohol Disinfecting Wipe 70 mL 68599-5803-04 McKesson 100 packets FDA listed
Hand Sanitizer 70 mL/100mL 70000-0579-01 Cardinal 135 ml FDA listed
Sani Luxe .7 mL/mL 71489-0009-01 Celeste 1.75 ml FDA listed
Signature Care Instant Hand Sanitizizer Wipes 70 g/100g 74149-0112-01 Yiwu 80 pouches FDA listed
Signature Care Instant Hand Sanitizer Wipes 70 g/100g 74149-0113-01 Yiwu 24 pouches FDA listed
Hand Sanitizer Wipes 70 mL/100mL 75214-0501-20 HANUL 134 ml FDA listed
Instant Hand Sanitizizer Wipes 70 g/100g 75262-0201-01 ZheJiang 80 pouches Discontinued
Tazza 70 mL/100mL 76370-0004-00 Tazza 40 applicators FDA listed
Tazza-X Hand Sanitizing Wipes 70 mL/100mL 76370-0008-00 Tazza 180 applicators Discontinued
Tazza-X Extreme Hand Sanitizing Wipes 70 mL/100mL 76370-0010-00 Tazza 50 pouches Discontinued
Singular Wipes 70 mL/100mL 81428-0070-04 SINGULAR 4 ml FDA listed
Singular Wipes lavender fragrance 70 mL/100mL 81428-0072-01 SINGULAR 30 pouches FDA listed
Travel Wipes Moisturizer and fragrance 70 mL/100mL 81428-0074-01 SINGULAR 15 pouches FDA listed
alcohol pad 01 .7 mL 82953-0012-01 Cosmuses 1 cloth FDA listed
Alcohol Cleansing Wipe .7 mL/mL 83165-0001-00 Hubei 1 patch FDA listed
Hand Sanitizing Wipes 70 mL/100mLthis 83986-0028-64 UpLift 20 packets FDA listed
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
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/100mL 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
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

🏛️
2023
On the market since
Nov 2023
📍
2026
Currently FDA-listed
3 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.

🔬 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 Hand Sanitizing Wipes (this brand).

Top reported reactions

Toxicity To Various Agents6,040
Completed Suicide5,450
Drug Abuse5,333
Overdose1,916
Death1,604
Intentional Overdose1,560
Suicide Attempt1,360

Age at onset

Neonate26
Infant15
Child16
Adolescent97
Adult2,874
Elderly309

Reporter sex

27,289 reports
Male · 54%
Female · 45%
Unknown · 0%

Serious outcomes

Hospitalization8,888
Reports over time (by year) — tap or hover for the count & year
2022 2023 2024 2026 2,604 1,504
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
83986-0028-64 You're viewing this 20 PACKET in 1 POUCH (83986-028-64) / 3 mL in 1 PACKET 2023-11-21 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 83986-028-64, 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: 83986-0028-64, written without dashes as 83986002864. 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 83986-0028-64, the first segment (83986) is the labeler code FDA assigned to UpLift Brands LLC; the middle segment (0028) identifies this specific product — its ingredient, strength, and dosage form; and the last segment (64) 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 UpLift Brands LLC. Listing status can change — the directory data on this page refreshes weekly.
Who lists this product with the FDA?
UpLift Brands LLC 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 7 words

Use to decrease bacteria on the skin

⏱️ Dosage and Administration 23 words

Directions wipe hands thoroughly with product and allow to dry 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 fire or flame.

🤒 Adverse Reactions 14 words

Adverse reaction Distributed by UpLift Brands, LLC St. Louis, MO 36114 1-866-MY-GERMX Pat. 9,161,982

📦 Storage and Handling 20 words

Other information do not store above 105º F may discolor some fabrics or surfaces harmful to wood finishes and plastics

🧪 Active Ingredient 6 words

Active ingredient Ethyl Alcohol 70% v/v

🧪 Inactive Ingredients 15 words

Inactive ingredients water, glycerin, glyceryl caprylate/caprate, Aloe barbadensis leaf juice, isopropyl myristate, tocopheryl acetate, fragrance

🎯 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 ↗
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.