PlaneAire Hands

ETHANOL HAND SANITIZER TOPICAL HUMAN OTC DRUG

PlaneAire Hands is an FDA drug label for the active ingredient ETHANOL HAND SANITIZER manufactured by EverywhereAire LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260706.

Generic name
ETHANOL HAND SANITIZER
Manufacturer
EverywhereAire LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
80335-112
Application
M003
Label effective
20260706

About this product

PlaneAire Hands is an FDA-registered drug product whose active ingredient is ETHANOL HAND SANITIZER. It is labelled by EverywhereAire LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 80335-112, application M003, label effective 20260706. It is one of 3 FDA drug label records sharing the active ingredient ETHANOL HAND SANITIZER. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ETHANOL HAND SANITIZER are most often described in connection with: hand sanitizer, help reduce, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient(s) Ethyl Alcohol 70% v/v

Indications & Usage

Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Dosage & Administration

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 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

Warnings For external use only on hands. Flammable. Keep away from heat and flame

More products with the same ingredient

ETHANOL HAND SANITIZER

PlaneAire Hands Lemon Olive Oil Hand Sanitizer

EverywhereAire LLC View label

PlaneAire Hands Sandalwood

EverywhereAire LLC View label

How products containing ETHANOL HAND SANITIZER compare

FDA lists 3 drug label records with ETHANOL HAND SANITIZER as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — EverywhereAire LLC 3
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Frequently asked questions

What is PlaneAire Hands used for?
Use Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Who makes PlaneAire Hands?
EverywhereAire LLC is the labeler of record for PlaneAire Hands. 3 FDA label records share the active ingredient ETHANOL HAND SANITIZER, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does PlaneAire Hands come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is PlaneAire Hands prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ETHANOL HAND SANITIZER?
Yes. 3 FDA drug label records list ETHANOL HAND SANITIZER as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has PlaneAire Hands been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.