North Woods Derma Foam Hand Sanitizer

North Woods Derma Foam Hand Sanitizer is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Superior Chemical Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 53125-700, application 505G(a)(3), label effective 20260909. 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.

Across FDA labelling, products containing BENZALKONIUM CHLORIDE are most often described in connection with: variety public. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Use in a variety of public facilities. Use this product when soap and water are not available.

Directions ​Read the entire label before using this product. ​Dispense product onto dry hands. Rub hands together until hands are dry. Use as needed between hand washes to reduce bacteria on the skin.

Warnings For external use only. Avoid contact with eyes. Children under the age of 6 should be supervised by an adult when using this product. Discontinue use is irritation or redness develops. If irritation persists for more than 72 hours, consult a physician. KEEP OUT OF REACH OF CHILDREN .

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.

What is North Woods Derma Foam Hand Sanitizer used for?
Uses Use in a variety of public facilities. Use this product when soap and water are not available.

Who makes North Woods Derma Foam Hand Sanitizer?
Superior Chemical Corporation is the labeler of record for North Woods Derma Foam 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 North Woods Derma Foam 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 North Woods Derma Foam 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 North Woods Derma Foam 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.