Antibacterial Hand Sanitizer Spray.

ETHYL ALCOHOL TOPICAL HUMAN OTC DRUG

Antibacterial Hand Sanitizer Spray. is an FDA drug label for the active ingredient ETHYL ALCOHOL manufactured by NANTONG HAIYIWEI TEXTILE CO., LTD. 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 20260717.

Generic name
ETHYL ALCOHOL
Manufacturer
NANTONG HAIYIWEI TEXTILE CO., LTD.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87858-003
Application
M003
Label effective
20260717

About this product

Antibacterial Hand Sanitizer Spray. is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by NANTONG HAIYIWEI TEXTILE CO., LTD. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87858-003, application M003, label effective 20260717. It is one of 184 FDA drug label records sharing the active ingredient ETHYL ALCOHOL. 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 ETHYL ALCOHOL are most often described in connection with: hand sanitizing, reduce bacteria. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Ethyl Alcohol 62%

Indications & Usage

Uses For hand sanitizing to reduce bacteria on the skin

Dosage & Administration

Directions Spray small amount in your palm and briskly rub hands together until dry.

Warnings

Warnings For external use only. Flammable. Keep away from fire or flame. When using this product o not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Discontinue use if irritation or redness develops. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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ETHYL ALCOHOL

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How products containing ETHYL ALCOHOL compare

FDA lists 184 drug label records with ETHYL ALCOHOL 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
— — Diamond Life Cosmetics Trading FZCO 33
— — Ashtel Studios, Inc. 30
— — Amber Glow Cosmetics Limited 22
— — PEACH LAYNE, LLC 10
— — Apollo Health and Beauty Care 8

Frequently asked questions

What is Antibacterial Hand Sanitizer Spray. used for?
Uses For hand sanitizing to reduce bacteria on the skin

Who makes Antibacterial Hand Sanitizer Spray.?
NANTONG HAIYIWEI TEXTILE CO., LTD. is the labeler of record for Antibacterial Hand Sanitizer Spray.. 184 FDA label records share the active ingredient ETHYL ALCOHOL, 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 Antibacterial Hand Sanitizer Spray. 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 Antibacterial Hand Sanitizer Spray. 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 ETHYL ALCOHOL?
Yes. 184 FDA drug label records list ETHYL ALCOHOL 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 Antibacterial Hand Sanitizer Spray. 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.