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Moisturizing Hand Sanitizer Ethyl Alcohol 62 mL/100mL Gel, 1150 mL — NDC 83986-447-45 (Billing 83986-0447-45)

by UpLift Brands, LLC · 1150 mL in 1 BOTTLE, PLASTIC

This is a package of 1,150 mL of Moisturizing Hand Sanitizer Ethyl Alcohol 62 mL/100mL Gel from UpLift Brands, LLC, marketed since Apr 2024 and currently FDA-listed. It is this product's only package size.

NDC 83986-0447-45
🏷️ FDA NDC (as labeled) 83986-447-45 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) 83986-447-45
Product NDC 83986-447
11-digit billing NDC 83986044745
UNII 3K9958V90M
Application # 505(a)(3)
SPL Set ID a1954926-35f6-439e-863f-29351013e554
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2024-04-12
Route TOPICAL
Dosage form GEL
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 83986-447-45 — 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 → 83986-0447-45. 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
83986-0447-45 You're viewing this Main listing 1150 mL in 1 BOTTLE, PLASTIC 2024-04-12 — Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
GENUINE FIRST AID Antiseptic Hand Sanitizer 62 mL/100mL 43473-0013-01 Nantong 1.03 ml — — FDA listed —
Antiseptic Hand Sanitizer 62 mL/100mL 76138-0113-16 Innovation 1 bottle — — FDA listed —
Hand Sanitizer 62 mL/100mL 83986-0815-16 UpLift 59 ml — — FDA listed —
5253 hand sanitizer 62 mL/100mL 76138-0117-02 Innovation 15 ml — — FDA listed —
Hand Sanitizer Lavender 62 mL/100mL 42681-0010-02 Whole 9 ml — — Discontinued —
everyone hand sanitizer wipes ruby grapefruit 62 mL/100mL 54748-0703-15 EO 6 packets — — FDA listed —
Instant Hand Sanitizer 62 mL/100mL 57337-0082-01 Rejoice 53 ml — — FDA listed —
Hillyard Instant Hand Sanitizer 62 mL/100mL 76402-0402-02 Hillyard 1000 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 62 mL/100mL 43473-0089-01 Nantong 9 ml — — FDA listed —
Antibacterial Hand Sanitizer 62 mL/100mL 71513-0105-01 Broder 29.57 ml — — FDA listed —
Thompson Hand Sanitizer 62 mL/100mL 73408-0512-73 Thompson 25 packets — — FDA listed —
Ethyl Alcohol 62 mL/100mL 83986-0969-34 UpLift 236 ml — — FDA listed —
Hand Sanitizer Lavender 62 mL/100mL 42681-7162-02 Whole 946 ml — — FDA listed —
Ethyl alcohol 62 mL/100mL 49035-0418-10 Walmart 29.5 ml — — FDA listed —
Ben E.Keith Hand Cleaner 62 mL/100mL 50980-0056-19 Ben 237 ml — — Discontinued —
everyone hand sanitizer wipes coconut lemon 62 mL/100mL 54748-0701-15 EO 6 packets — — FDA listed —
Hand Sanitizer 62 mL/100mL 71927-0005-01 Orazen 44 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 71927-0008-01 Orazen 30 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 76138-0114-13 Innovation 30 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 65692-1003-01 Raining 17 ml — — FDA listed —
5259 Hand Sanitizer 62 mL/100mL 76138-0120-04 Innovation 40 ml — — FDA listed —
EVERLIT CARE Hand Sanitizer 62 mL/100mL 83807-0003-01 EVERLIT 9 ml — — FDA listed —
Moisturizing Hand Sanitizer 62 mL/100mLthis 83986-0447-45 UpLift 1150 ml — — FDA listed —
Instant Hand Sanitizer 62 mL/100mL 57337-0084-01 Rejoice 53 ml — — FDA listed —
Lightning X Hand Cleanser 62 mL/100mL 43473-0122-01 Nantong 9 ml — — FDA listed —
Medline 62 mL/100mL 53329-0121-09 Medline 1 applicator — — FDA listed —
everyone hand sanitizer wipes lavender aloe 62 mL/100mL 54748-0702-15 EO 6 packets — — FDA listed —
5406 hand sanitizer 62 mL/100mL 76138-0116-03 Innovation 30 ml — — FDA listed —
Moisturizing Hand Sanitizer 62 mL/100mL 83986-0849-16 UpLift 59 ml — — FDA listed —
Spectrum 62% Hand Sanitizer 62 mL/100mL 53329-0214-13 Medline 59.147 ml — — Discontinued —
Instant Hand Sanitizer 62 mL/100mL 57337-0083-01 Rejoice 53 ml — — FDA listed —
Hand Sanitizer 62 mL/100mL 71927-0001-01 Orazen 30 ml — — Discontinued —
Frosted Cherry Scented Hand Sanitizer 62 mL/100mL 60193-0001-00 Pacific 1 bottle — — FDA listed —
Gingerbread Scented Hand Sanitizer 62 mL/100mL 60193-0002-00 Pacific 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

🏛️
2024
On the market since
Apr 2024
📍
2026
Currently FDA-listed
2 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

LabelerUpLift Brands, LLC
FDA application505(a)(3) (OTC MONOGRAPH DRUG)
Labeler code83986
First marketedApr 2024
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.

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 🤒 Adverse Reactions 📦 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 15 words ▾

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

⏱️ Dosage and Administration 25 words ▾

Directions wet hands thoroughly with product and allow to dry without wiping for children under 6, use only under adult supervision not recommended for infants

⚠️ Warnings 14 words ▾

Warnings For external use only: hands Flammable, keep away from fire or flame .

🤒 Adverse Reactions 16 words ▾

Adverse Reactions DISTRIBUTED BY: UPLIFT BRANDS, LLC ST. LOUIS, MO 63114 1-866 MY GERMX DSP-TN-21091 DSP-MO-20087

📦 Storage and Handling 18 words ▾

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

🧪 Active Ingredient 5 words ▾

Active ingredient Ethyl alcohol 62%

🧪 Inactive Ingredients 12 words ▾

Inactive ingredients water, PEG-8 dimethicone, meadowfoamamidopropyl betaine, glycerin, tocopheryl acetate, isopropyl myristate

🎯 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 18 words ▾

Stop use and ask a doctor if irritation and redness develop condition persists for more than 72 hours

📄 Keep Out of Reach of Children 19 words ▾

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

📄 Package Label / Principal Display Panel 21 words ▾

Principal display panel germ-X ® PRO MOISTURIZING FOAMING HAND SANITIZER 1150 mL (1.21 QT) 39 FL OZ image description 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 Moisturizing Hand Sanitizer (this brand).

Top reported reactions

Drug Abuse48
Toxicity To Various Agents31
Overdose27
Intentional Overdose19
Poisoning Deliberate19
Suicide Attempt19
Completed Suicide18

Age at onset

Adolescent2
Adult30
Elderly5

Reporter sex

0 reports
Male · 61%
Female · 39%

Serious outcomes

Hospitalization99
Death74
Life-threatening10
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 21 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 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.
← 83986-0439-16 · UpLift 83986-0456-04 · UpLift →
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.