Home › NDC Lookup › Ingredients › Alcohol › 69662-0111-02
Refresher alcohol 65 mL/100mL Liquid, 59 mL — NDC 69662-0111-02 package photo

Refresher alcohol 65 mL/100mL Liquid, 59 mL

by Jao Limited · 59 mL in 1 BOTTLE, SPRAY (69662-111-02)
NDC 69662-0111-02
🏷️ FDA NDC (as labeled) 69662-111-02 billing pads the product segment with a zero
This package
Contains59 mL Pack sizes5 compare ↓
Also comes in: 118 ml 69662-0111-03 236 ml 69662-0111-01 840 ml 69662-0111-05 3750 ml 69662-0111-04
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) 69662-111-02
Product NDC 69662-111
11-digit billing NDC 69662011102
RxCUI 884783
UNII 3K9958V90M
Application # M003
SPL Set ID 1debc8ca-2ea4-40c3-ad1e-8c1dc763d0f8
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2016-03-30
Route TOPICAL
Dosage form LIQUID
Substance ALCOHOL
Why two NDCs? The FDA registers this code as 69662-111-02 — 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 → 69662-0111-02. 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.

🏷️ 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

LabelerJao Limited
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code69662
First marketedMar 2016
Product typeHuman Otc Drug
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 XLW9XG1719
    A waxy compound made from sucrose (sugar) and stearic acid. It acts as an emulsifier to blend water and oil ingredients, and helps create a smooth texture in the medicine.
  • UNII PI80E777XB
    A synthetic plastic polymer used as a tablet or capsule coating. It helps control how quickly the medicine dissolves and protects the ingredient inside from stomach acid, allowing release in the intestines instead.
  • 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 LU49E6626Q
    A synthetic organic compound used as a pH buffer and neutralizing agent in medicines. It helps maintain the proper acidity level in liquid formulations to improve stability and comfort.
  • UNII 3U3U118F2L
    A plant extract from calendula flowers used as a natural colorant and flavoring agent in medicines. It may add color or mild taste to the product.
  • UNII FGL3685T2X
    Chamomile is a plant extract used in medications as a flavoring agent and for its mild soothing properties in formulations. It helps improve taste and aroma of the medicine.
  • UNII 2R04ONI662
    Eucalyptus oil is a fragrant liquid extracted from eucalyptus tree leaves. It's used in medicines as a flavor, scent, or soothing agent in topical products and cough preparations.
  • UNII 5Q1I94P4WG
    A fragrant essential oil derived from geranium plants, used as a flavoring and fragrance agent to improve the taste and smell of medicines.
  • 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 W2ZU1RY8B0
    A plant extract from green tea leaves. It's used as an antioxidant ingredient to help preserve the medicine and maintain its stability during storage.
  • UNII ZBP1YXW0H8
    A fragrant oil extracted from lavender plants, used as a flavoring and scent agent in medicines to improve taste and aroma.
  • UNII WV9CM0O67Z
    Panthenol is a humectant and skin-conditioning agent derived from pantothenic acid. It's added to medicines to help retain moisture and soothe skin irritation.
  • UNII 7T1F30V5YH
    A synthetic emulsifier derived from sorbitol and oleic acid. It helps mix oil and water-based ingredients together and keeps them from separating in liquid formulations.
  • UNII U27K0H1H2O
    Sage oil is a plant-derived liquid extracted from sage leaves. It's used in medicines as a flavoring agent and preservative to improve taste and help protect the product from spoilage.
  • 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.

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

The official label also statesAcrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis, Amino-Methyl Propanol, Calendula Extract, Chamomile Extract, dl-Panthenol, Essential Oils (Lavender, Tea Tree, Eucalyptus, Geranium, Clary Sage), Glycerine and Glyceryl Polyacrylate, PPG-20 Methyl Glucose Ether Distearate, Water

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 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: 118 ml 236 ml 840 ml 3750 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.

🔁 Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
Discount Drug Mart Vitamin E Hand Sanitizer 650 mg/mL 53943-0022-32 Discount 946 ml — — FDA listed —
Hand sanitizer 29ml 01 65 mL/100mL 54860-0415-01 Shenzhen 29 ml — — FDA listed —
FIGS evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented 65 mL/100mL 56152-1471-01 Cosmetic 10 ml — — FDA listed —
Refresher 65 mL/100mLthis 69662-0111-02 Jao 59 ml — — FDA listed —
Iso-Quin hand sanitizer 65 mL/100mL 82345-0858-10 The 3785 ml — — FDA listed —
Koala Eco Hand Sanitizer 650 mg/mL 87177-0001-01 Koala 89 ml — — FDA listed —
FIGS - evolvetogether Hand Sanitizer FIGS 01 Ginger - Cedar Scented 65 mL/100mL 87495-0065-01 WE 3 vials — — 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

🏛️
2016
On the market since
Mar 2016
📍
2026
Currently FDA-listed
10 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 Alcohol — the ingredient across all brands.

Top reported reactions

Completed Suicide8,269
Toxicity To Various Agents7,836
Drug Abuse6,970
Death3,095
Overdose2,500
Vomiting2,257
Fatigue2,251

Age at onset

Neonate54
Infant28
Child35
Adolescent107
Adult4,432
Elderly1,243

Reporter sex

46,735 reports

Serious outcomes

Death25,134
Life-threatening4,440
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 3,979 1,870
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
69662-0111-01 236 mL in 1 BOTTLE, PUMP (69662-111-01) 2016-04-06 Active
69662-0111-02 You're viewing this 59 mL in 1 BOTTLE, SPRAY (69662-111-02) 2016-04-06 Active
69662-0111-03 118 mL in 1 BOTTLE, SPRAY (69662-111-03) 2016-05-04 Active
69662-0111-04 3750 mL in 1 JUG (69662-111-04) 2017-07-20 Active
69662-0111-05 840 mL in 1 POUCH (69662-111-05) 2020-06-29 Active

You're viewing the smallest of 5 pack sizes for this product.

Pack size FAQ

What quantity is in NDC 69662-0111-02?
NDC 69662-0111-02 contains 59 mL — 59 ml in 1 bottle, spray.
What is the difference between NDC 69662-0111-02 and NDC 69662-0111-03?
Both are Refresher alcohol 65 mL/100mL Liquid — the drug itself is identical. NDC 69662-0111-02 is the 59 mL package, while NDC 69662-0111-03 is the 118 ml package.
What NDC number is used to bill for this package of Refresher alcohol 65 mL/100mL Liquid?
Bill NDC 69662-0111-02 — the 11-digit billing format is 69662011102. Pharmacy and medical claims use the 11-digit form; the FDA label may print a shorter form of the same code.

🧭 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 69662-111-02, 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: 69662-0111-02, written without dashes as 69662011102. 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 69662-0111-02, the first segment (69662) is the labeler code FDA assigned to Jao Limited; the middle segment (0111) 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 Jao Limited. 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 118 ml (69662-0111-03), 236 ml (69662-0111-01), 840 ml (69662-0111-05). 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?
Jao Limited 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 15 words ▾

Uses: Sanitizer to help reduce bacteria on skin. For use when water is not available.

⏱️ Dosage and Administration 8 words ▾

Directions Apply on hands, rub briskly until dry.

⚠️ Warnings 12 words ▾

Warnings For external use only. Flammable. Keep away from heat or flame.

🧪 Active Ingredient 5 words ▾

Active Ingredient Ethyl Alcohol 65%

🧪 Inactive Ingredients 34 words ▾

Inactive Ingredients Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis, Amino-Methyl Propanol, Calendula Extract, Chamomile Extract, dl-Panthenol, Essential Oils (Lavender, Tea Tree, Eucalyptus, Geranium, Clary Sage), Glycerine and Glyceryl Polyacrylate, PPG-20 Methyl Glucose Ether Distearate, Water

🎯 Purpose 2 words ▾

Purpose Antimicrobial

Source: FDA Structured Product Labeling, mirrored from DailyMed / openFDA. Prefer the government’s original formatting? View this label on DailyMed ↗
← 69654-0584-30 · Aytu 69664-0001-01 · Momentum →
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.