Signature Series Enriched Foam Alcohol Hand Sanitizer

ALCOHOL TOPICAL HUMAN OTC DRUG

Signature Series Enriched Foam Alcohol Hand Sanitizer is an FDA drug label for the active ingredient ALCOHOL manufactured by Cintas 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 20260605.

Generic name
ALCOHOL
Manufacturer
Cintas
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
42961-017
Application
505G(a)(3)
Label effective
20260605

About this product

Signature Series Enriched Foam Alcohol Hand Sanitizer is an FDA-registered drug product whose active ingredient is ALCOHOL. It is labelled by Cintas taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 42961-017, application 505G(a)(3), label effective 20260605. 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: decrease potentially, harmful germs. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient Alcohol Denat. 75% (v/v)

Indications & Usage

Use To decrease potentially harmful germs on skin.

Dosage & Administration

Directions Apply generously to hands. Rub hands together. Allow hands to dry. Repeat daily as necessary.

Warnings

Warnings Flammable. Keep away from fire or flame. For external use only. When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and ask a doctor if irritation of redness develops or if condition persists for more than 72 hours. Keep out of reach of children. If swallowed , do not induce vomiting, get medical attention. Read material safety data sheet before using product

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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 Signature Series Enriched Foam Alcohol Hand Sanitizer used for?
Use To decrease potentially harmful germs on skin.

Who makes Signature Series Enriched Foam Alcohol Hand Sanitizer?
Cintas is the labeler of record for Signature Series Enriched Foam 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 Signature Series Enriched Foam 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 Signature Series Enriched Foam 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 Signature Series Enriched Foam 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.