Summit 375 Gel Alcohol Hand Sanitizer

ALCOHOL TOPICAL HUMAN OTC DRUG

Summit 375 Gel Alcohol Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by R.L. Williams Company 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 20260429.

Generic name
ALCOHOL
Manufacturer
R.L. Williams Company
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
23590-400
Application
505G(a)(3)
Label effective
20260429

About this product

Summit 375 Gel Alcohol Hand Sanitizer is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by R.L. Williams Company taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 23590-400, application 505G(a)(3), label effective 20260429. 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 sanitizer, help reduce, 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 70% v/v

Indications & Usage

Uses Hand sanitizer to help reduce bacteria on the skin Recommended for repeated use

Dosage & Administration

Directions Dispense an adequate amount in your palm to cover all surface of hands completely. Rub hands together until dry. Supervise children in the use of this product.

Warnings

Warnings Flammable, keep away from fire or flame . For external use only . When using this product do not use around or near the eyes. If contact occurs, flush eyes with water and contact a doctor immediately. Stop use and ask a doctor if irritation and redness develop and persist 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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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 Summit 375 Gel Alcohol Hand Sanitizer used for?
Uses Hand sanitizer to help reduce bacteria on the skin Recommended for repeated use

Who makes Summit 375 Gel Alcohol Hand Sanitizer?
R.L. Williams Company is the labeler of record for Summit 375 Gel Alcohol Hand Sanitizer. 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 Summit 375 Gel 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 Summit 375 Gel 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 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 Summit 375 Gel Alcohol Hand Sanitizer 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.