Spectrum Hand Sanitizer Wipes

ETHYL ALCOHOL TOPICAL HUMAN OTC DRUG

Spectrum Hand Sanitizer Wipes is an FDA drug label for the active ingredient ETHYL ALCOHOL manufactured by Medline Industries, LP 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 20260715.

Generic name
ETHYL ALCOHOL
Manufacturer
Medline Industries, LP
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
53329-840
Application
505G(a)(3)
Label effective
20260715

About this product

Spectrum Hand Sanitizer Wipes is an FDA-registered drug product whose active ingredient is ETHYL ALCOHOL. It is labelled by Medline Industries, LP taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 53329-840, application 505G(a)(3), label effective 20260715. 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: decrease bacteria, cause disease. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Ethyl alcohol 70%

Indications & Usage

Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Dosage & Administration

Directions wet hands thoroughly with product and allow to dry without wiping not recommended for infants

Warnings

Warnings For external use only: hands Flammable. Keep away from fire and flame. When using this product keep out of eyes. In case of contact with eyes, flush thoroughly with water. avoid contact with broken skin do not inhale or ingest Stop Use and ask a doctor if irritation or redness develops condition persists for more than 72 hours 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

Recall and safety notices

5 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-0035-2026 Medline, Alcohol Prep Pads (2-Ply Pad, 70% Isopropyl Alcohol), 100 eaches per box, 10 boxes per case (1,000 eaches per case), Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL, 60093 USA, NDC 55329-811-30. Medline Industries, LP Class II Ongoing 20251029
D-0674-2025 READYPREP PVP, Povidone-Iodine 10% Solution, Topical Antiseptic, Not Sterile, 1 Gallon (3.78 L) per bottle, Manufactured in USA by Medline Industries, LP., Three Lakes Drive, Northfield, IL 60093, NDC 53329-939-25 Medline Industries, LP Class III Ongoing 20251001
D-0604-2025 Good Neighbor Pharmacy, Alcohol Prep Pads, Distributed By AmeriSource Bergen, 1 West First Avenue, Conshohocken, PA 19428, Made in China: 100 eaches per box, 30 boxes per case, (3,000 eaches per case), NDC 46122-043-78. MEDLINE INDUSTRIES, LP - Northfield Class II Ongoing 20250903
D-0602-2025 ReliOn, Sterile Alcohol Swabs, Skin Cleanser, 200 Swabs, Distributed by, Walmart, Inc., Bentonville, AR 72716 Walmart: 200 eaches per box, 24 boxes per case (4,800 eaches per case), NDC 49035-814-60. MEDLINE INDUSTRIES, LP - Northfield Class II Ongoing 20250903
D-0601-2025 CURAD Alcohol Prep Pads, Sterile, Medium, 2-Ply, Contents: 5 boxes per Carton, 30 Boxes per Case, Single Use Only, Manufactured for Medline Industries, LP, Three Lakes Drive, Northfield, IL 60093, USA, Made in India, www.curad.com, 1-800-633-5463, NDC 53329-827-30 MEDLINE INDUSTRIES, LP - Northfield Class II Ongoing 20250903

Frequently asked questions

What is Spectrum Hand Sanitizer Wipes used for?
Uses to decrease bacteria on the skin that could cause disease recommended for repeated use

Who makes Spectrum Hand Sanitizer Wipes?
Medline Industries, LP is the labeler of record for Spectrum Hand Sanitizer Wipes. 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 Spectrum Hand Sanitizer Wipes 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 Spectrum Hand Sanitizer Wipes 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 Spectrum Hand Sanitizer Wipes been recalled?
5 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.