3M Avagard D

ALCOHOL TOPICAL HUMAN OTC DRUG

3M Avagard D is an FDA drug label for the active ingredient ALCOHOL manufactured by Solventum US 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 20260422.

Generic name
ALCOHOL
Manufacturer
Solventum US LLC
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
17518-050
Application
M003
Label effective
20260422

About this product

3M Avagard D is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Solventum US LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 17518-050, application M003, label effective 20260422. It is one of 582 FDA drug label records sharing the active ingredient 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 ALCOHOL are most often described in connection with: hand antiseptic, instant healthcare, reduce bacteria, cause disease, skin recommended. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient Ethyl Alcohol, 61% w/w

Indications & Usage

Uses instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease instant hand antiseptic to decrease bacteria on the skin recommended for repeated use

Dosage & Administration

Directions Apply to clean, dry hands. Apply sufficient amount to thoroughly wet all surfaces of hand and fingers. Rub on to hands until dry. Supervise children in the use of this product.

Warnings

Warnings For external use only. Flammable, keep away from fire or flames. When using this product keep out of eyes. If contact with eyes occurs, rinse promptly and thoroughly with water. Stop use and ask a doctor if significant irritation or sensitization develops. 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 ALCOHOL compare

FDA lists 582 drug label records with 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
— — Bath & Body Works, Inc. 79
— — Shenzhen Lantern Scicence Co.,Ltd. 66
— — Fourstar Group USA, Inc. 41
— — Church & Dwight Co., Inc. 33
— — Target Corporation 23

Frequently asked questions

What is 3M Avagard D used for?
Uses instant healthcare personnel hand antiseptic to reduce bacteria that potentially can cause disease instant hand antiseptic to decrease bacteria on the skin recommended for repeated use

Who makes 3M Avagard D?
Solventum US LLC is the labeler of record for 3M Avagard D. 582 FDA label records share the active ingredient 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 3M Avagard D 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 3M Avagard D 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 ALCOHOL?
Yes. 582 FDA drug label records list 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 3M Avagard D 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.