Alcohol Hand Sanitizer

ETHYL ALCOHOL TOPICAL HUMAN OTC DRUG

Alcohol Hand Sanitizer is an FDA drug label for the active ingredient ETHYL ALCOHOL manufactured by Guangdong Yanze Biotechnology 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 20260813.

Generic name
ETHYL ALCOHOL
Manufacturer
Guangdong Yanze Biotechnology Co., Ltd.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87660-001
Application
M003
Label effective
20260813

About this product

Alcohol Hand Sanitizer is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Guangdong Yanze Biotechnology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87660-001, application M003, label effective 20260813. 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 sanitizer, help reduce. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients Ethyl Alcohol 60%

Indications & Usage

Use Hand sanitizer to help reduce bacteria on the skin.

Dosage & Administration

Directions • Place enough product in your palm to thoroughly spread on both hands and rub into the skin until dry. • Children under 6 years of age should be supervised when using this product.

Warnings

Warnings Flammable. Keep away from fire when using. For external use only. When using this product do not use near the eyes in case of contact, rinse eyes thoroughly with water. Stop use and ask doctor if irritation or rash appears and lasts. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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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

Recall and safety notices

1 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

RecallProductFirmClassStatusReported
D-0666-2021 Ulta beauty Fresh Lemon Citron Frais, 70% Alcohol Hand Sanitizer Spray, Net Wt. 100.55/3.4 fl. oz., UPC 717897092017 Scentsational Soaps & Candles Inc Class I Terminated 20210728

Frequently asked questions

What is Alcohol Hand Sanitizer used for?
Use Hand sanitizer to help reduce bacteria on the skin.

Who makes Alcohol Hand Sanitizer?
Guangdong Yanze Biotechnology Co., Ltd. is the labeler of record for Alcohol Hand Sanitizer. 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 Alcohol Hand Sanitizer 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 Alcohol Hand Sanitizer 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 Alcohol Hand Sanitizer been recalled?
1 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.