Germ Free 24 Hand Sanitizer

BENZALKONIUM CHLORIDE TOPICAL HUMAN OTC DRUG

Germ Free 24 Hand Sanitizer is an FDA drug label for the active ingredient BENZALKONIUM CHLORIDE manufactured by Enviro Specialty Chemicals Inc 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 20260721.

Generic name
BENZALKONIUM CHLORIDE
Manufacturer
Enviro Specialty Chemicals Inc
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
71884-006
Application
505G(a)(3)
Label effective
20260721

About this product

Germ Free 24 Hand Sanitizer is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Enviro Specialty Chemicals Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71884-006, application 505G(a)(3), label effective 20260721. It is one of 231 FDA drug label records sharing the active ingredient BENZALKONIUM CHLORIDE. 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 BENZALKONIUM CHLORIDE are most often described in connection with: hand sanitizer, help decrease, skin recommended. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active Ingredient: Benzalkonium Chloride 0.13%

Indications & Usage

Uses: Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

Dosage & Administration

Directions: Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use.

Warnings

Warnings: Do not freeze. For external use only. Do not use in ears, eyes or mouth. • When using this product, avoid contact with the eyes. In case of contact, flush eyes with water. • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. • Keep out of reach of children. • Children should be supervised when using this product.

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How products containing BENZALKONIUM CHLORIDE compare

FDA lists 231 drug label records with BENZALKONIUM CHLORIDE 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
— — USA Broom LLC 28
— — Apollo Health and Beauty Care 11
— — Enviro Specialty Chemicals Inc 11
— — H E B 10
— — Jianerkang Medical Co., Ltd 7

Frequently asked questions

What is Germ Free 24 Hand Sanitizer used for?
Uses: Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

Who makes Germ Free 24 Hand Sanitizer?
Enviro Specialty Chemicals Inc is the labeler of record for Germ Free 24 Hand Sanitizer. 231 FDA label records share the active ingredient BENZALKONIUM CHLORIDE, 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 Germ Free 24 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 Germ Free 24 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 BENZALKONIUM CHLORIDE?
Yes. 231 FDA drug label records list BENZALKONIUM CHLORIDE 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 Germ Free 24 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.