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PlaneAire Hands hand sanitizer Hand sanitizer ethanol-based 70 mL/100mL Lotion, 60 mL — NDC 80335-0115-02 package photo
Label image from the product's FDA listing (DailyMed) — may show a different pack size or an older label revision.

PlaneAire Hands hand sanitizer Hand sanitizer ethanol-based 70 mL/100mL Lotion, 60 mL — NDC 80335-115-02 (Billing 80335-0115-02)

by EverywhereAire LLC · 60 mL in 1 BOTTLE, PUMP

This is a package of 60 mL of PlaneAire Hands hand sanitizer Hand sanitizer ethanol-based 70 mL/100mL Lotion from EverywhereAire LLC, marketed since Oct 2022 and currently FDA-listed, this package's marketing is listed to end Dec 2026. It is this product's only package size.

NDC 80335-0115-02
🏷️ FDA NDC (as labeled) 80335-115-02 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

NDC database record

One package, one record: these facts belong to NDC 80335-115-02 alone.

Record
FDA NDC Directory package listing · Human OTC drug
Code segments
80335 labeler · 115 product · 02 package
Package marketed since
Oct 24, 2022
Package marketing ended
Dec 31, 2026
Sample package
No — commercial package
Barcode (UPC)
0850001608879
FDA record last changed
Jul 24, 2026

Identity & classification

Regulatory identifiers FDA, NLM and CMS codes for this package

FDA NDC (as labeled) 80335-115-02
Product NDC 80335-115
11-digit billing NDC 80335011502
RxCUI 1809903
UNII 3K9958V90M
UPC 0850001608879
Application # M003
SPL Set ID eab19649-21fc-2fa4-e053-2995a90a90f9
DEA schedule Non-controlled
Marketing category OTC MONOGRAPH DRUG
Marketing status On market
FDA listing status Listed (active directory)
Marketing start 2022-10-24
Marketing end 2026-12-31
Route TOPICAL
Dosage form LOTION
Substance ALCOHOL
Quick answers
  • RxCUI (RxNorm): 1809903
Why two NDCs? The FDA registers this code as 80335-115-02 — 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 → 80335-0115-02. 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.

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
80335-0115-02 You're viewing this Main listing 60 mL in 1 BOTTLE, PUMP 2022-10-24 Dec 31, 2026 Active

Therapeutic equivalents

ProductLabelerPackNADAC/unitTEStatusPrice vs. this
DermaCen Lotionized Hand Sanitizer 70 mL/100mL 62654-0151-64 Central 236 ml — — FDA listed —
Hand Sanitizer 70 mL/100mL 68599-5207-01 McKesson 237 ml — — FDA listed —
Hand 70 mL/100mL 70741-0006-02 Derma 40 ml — — FDA listed —
Hand Recovery 70 mL/100mL 70741-0007-06 Derma 947.2 ml — — FDA listed —
Hand Relief 70 mL/100mL 70741-0012-05 Derma 480 ml — — FDA listed —
PlaneAire Hands hand sanitizer 70 mL/100mLthis 80335-0115-02 EverywhereAire 60 ml — — FDA listed —
PlaneAire Hands 70 mL/100mL 80335-0116-02 EverywhereAire 60 ml — — FDA listed —
PlaneAire Hands Sandalwood 70 mL/100mL 80335-0118-02 EverywhereAire 60 ml — — FDA listed —
PlaneAire Hands Lemon Olive Oil Hand Sanitizer 70 mL/100mL 80335-0119-02 EverywhereAire 60 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

🏛️
2022
On the market since
Oct 2022
📍
2026
Currently FDA-listed
4 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.

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

  • UNII W21O437517
    A natural substance extracted from aloe vera leaves, used as a thickener and emulsifier to improve texture and help mix oil and water-based ingredients in the medicine.
  • UNII JM0KJ091HZ
    A natural oil extracted from cardamom seeds, used as a flavoring agent and solvent in medicines to improve taste and help dissolve or distribute other ingredients.
  • UNII 9S60Q72309
    A plant-derived ingredient made from safflower seed components. It acts as an emulsifier and carrier to help distribute oils and active ingredients evenly throughout the medicine.
  • UNII RYQ4R60M02
    A green algae ingredient used as a natural colorant and nutritional filler in supplements and medications. It adds color and bulk to tablets and capsules.
  • 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 44P1VFO6KM
    A natural oil extracted from lingonberry seeds, used as a source of fatty acids and antioxidants. It may function as a skin-conditioning agent or emollient in topical formulations.
  • UNII 05I15JNI2J
    A synthetic polymer that absorbs and holds moisture. Used in tablets and capsules as a super-disintegrant to help the medicine break apart quickly when swallowed, allowing faster drug release.
  • UNII 9L3TIH1UUE
    Spirulina platensis is a blue-green algae used as a natural colorant and nutritional ingredient in supplements and some medications. It provides a blue-green color and may add protein and vitamins to the product.
  • 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.

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

The official label also statesAloe Vera (Inner Leaf),Cardamom Oil (Elettaria Cardamomum), Chlorella Vulgaris Powder, Glycerin, Green Tea Extract (Camellia Sinensis Leaf), Lavender (Lavandula Angustifolia) Oil, Lingonberry (Vaccinium Vitis-Idaea) Seed Oil, Polyacrylate Crosspolymer-6, Safflower Seed Oil (Carthamus Tinctorius), Spirulina Platensis Powder, 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.

Manufacturer & labeler

LabelerEverywhereAire LLC
FDA applicationM003 (OTC MONOGRAPH DRUG)
Labeler code80335
First marketedOct 2022
Product typeHuman Otc Drug
Portfolio9 products on file

More NDCs from EverywhereAire LLC labeler code 80335

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 📦 Storage and Handling 🧪 Active Ingredient 🧪 Inactive Ingredients 🎯 Purpose 📄 Do Not Use 📄 Stop Use and Ask a Doctor If 📄 Keep Out of Reach of Children 📄 Recent Major Changes 📄 Package Label / Principal Display Panel
🎯 Indications and Usage 22 words ▾

Uses helps reduce bacteria that potentially can cause disease for use when soap and water are not available Uses Sectiin category updated

⏱️ Dosage and Administration 33 words ▾

Directions Wet hands thoroughly with product, rub hands, and allow to dry without wiping. For children under 6 years of age, use only under adult supervision to avoid swallowing. not recommended for infants

⚠️ Warnings 71 words ▾

Warnings For external us eonly- on hands. Flammable. Keep away from heat and flame Do not use on open wounds or near eyes. In case of contact with eyes, rinse thoroughly with water. Discontinue use if irritation or redness develops If condition persists for more than 72 hours, consult a doctor Keep out of reach of children If swallowed, get medical help or contact a local Poison Control Center right away

📦 Storage and Handling 26 words ▾

Other Information store between 15-30C ( 59-86F) do not store above 105F avoid freezing may discolor fabrics may be harmful to some wood finishes and plastics

🧪 Active Ingredient 6 words ▾

Active Ingredient Ethyl Alcohol 70% v/v

🧪 Inactive Ingredients 44 words ▾

Inactive Ingredients Aloe Vera (Inner Leaf),Cardamom Oil ( Elettaria Cardamomum), Chlorella Vulgaris Powder, Glycerin, Green Tea Extract ( Camellia Sinensis Leaf), Lavender ( Lavandula Angustifolia) Oil, Lingonberry ( Vaccinium Vitis-Idaea) Seed Oil, Polyacrylate Crosspolymer-6, Safflower Seed Oil (Carthamus Tinctorius), Spirulina Platensis Powder, Water (Aqua)

🎯 Purpose 2 words ▾

Purpose Antiseptic

📄 Do Not Use 19 words ▾

Do not use on open wounds or near eyes. In case of contact with eyes, rinse thoroughly with water.

📄 Stop Use and Ask a Doctor If 18 words ▾

Discontinue use if irritation or redness develops If condition persists for more than 72 hours, consult a doctor

📄 Keep Out of Reach of Children 20 words ▾

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

📄 Recent Major Changes 4 words ▾

Uses Sectiin category updated

📄 Package Label / Principal Display Panel 3 words ▾

package label 80335-115

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 Ethyl Alcohol — the ingredient across all brands.

Top reported reactions

Toxicity To Various Agents6,039
Completed Suicide5,452
Drug Abuse5,334
Overdose1,918
Death1,602
Intentional Overdose1,560
Suicide Attempt1,359

Age at onset

Neonate26
Infant14
Child18
Adolescent94
Adult2,855
Elderly321

Reporter sex

27,244 reports
Male · 54%
Female · 45%
Unknown · 0%

Serious outcomes

Death15,216
Hospitalization8,770
Life-threatening1,422
Disabling222
Reports over time (by year) — tap or hover for the count & year
2019 2021 2023 2026 2,695 1,502
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 ✓ 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 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 it is currently marketed — but EverywhereAire LLC has reported a marketing end date of 2026-12-31, after which this package is expected to stop being marketed. The directory data on this page refreshes weekly.
Who lists this product with the FDA?
EverywhereAire 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.
← 80335-0114-02 · EverywhereAire 80335-0116-02 · EverywhereAire →
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.