Dr Lift Advanced Antibacterial Wipes

Dr Lift Advanced Antibacterial Wipes is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE. It is labelled by Spa de Soleil taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 68062-2244, application M003, label effective 20260430. 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: hands rub, together briskly, dispose wipe, directions take, allow air, flush dispense, peel back, front label. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Directions Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry and allow to air dry. Dispose of wipe in trash. Do not flush. To Dispense: Peel back front label slowly. Remove Wipes. To Reseal: Firmly run thumb over the label. Dispose of wipe in trash. Do not flush. Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry. Inactive Ingredients:

Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands together briskly until product is completely absorbed and hands are dry. Inactive Ingredients:

Warnings Warnings For external use only. Do not use if you are allergic to any of these ingredients. If product gets in eyes, rinse promptly and thoroughly with water. Discontinue use if irritation and redness occur. Stop use and ask a doctor if irritation or redness lasts for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

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 Dr Lift Advanced Antibacterial Wipes used for?
Directions Take wipe and rub thoroughly over all surfaces of both hands. Rub hands together briskly to dry and allow to air dry. Dispose of wipe in trash. Do not flush. To Dispense: Peel back front label slowly. Remove Wipes. To Reseal: Firmly run thumb over the label. Dispose of wipe in trash. Do not flush. Place enough product in the palm of your hands to thoroughly cover you hands. Rub hands …

Who makes Dr Lift Advanced Antibacterial Wipes?
Spa de Soleil is the labeler of record for Dr Lift Advanced Antibacterial Wipes. 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 Dr Lift Advanced Antibacterial Wipes 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 Dr Lift Advanced Antibacterial Wipes 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 Dr Lift Advanced Antibacterial Wipes 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.