Benzethonium chloride and Dyclonine hydrochloride

Benzethonium chloride and Dyclonine hydrochloride is an FDA-registered drug product whose active ingredient is LIQUID BANDAGE. It is labelled by Target Corporation taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 82442-019, application M003, label effective 20260622. It is one of 5 FDA drug label records sharing the active ingredient LIQUID BANDAGE. 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 LIQUID BANDAGE are most often described in connection with: first aid, minor cuts, help prevent, temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses first aid to help prevent infection in minor cuts, scrapes and burns first aid for the temporary relief of pain in minor cuts, scrapes, and burns

Directions for adults and children 2 years of age and older clean the affected area apply a small amount of this product on the area 1 to 3 times daily and let dry may be covered with a sterile bandage if bandaged, let dry first children under 2 years of age: do not use, consult doctor

Warnings For external use only. Flammable: Keep away from fire or flame. Do not use in the eyes over large areas of the body longer than 1 week unless directed by a doctor Ask a doctor before use if you have deep or puncture wounds animal bites serious burns Stop use and ask a doctor if conditions persists or gets worse infection occurs symptoms persist for more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

FDA lists 5 drug label records with LIQUID BANDAGE 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 Benzethonium chloride and Dyclonine hydrochloride used for?
Uses first aid to help prevent infection in minor cuts, scrapes and burns first aid for the temporary relief of pain in minor cuts, scrapes, and burns

Who makes Benzethonium chloride and Dyclonine hydrochloride?
Target Corporation is the labeler of record for Benzethonium chloride and Dyclonine hydrochloride. 5 FDA label records share the active ingredient LIQUID BANDAGE, 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 Benzethonium chloride and Dyclonine hydrochloride 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 Benzethonium chloride and Dyclonine hydrochloride 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 LIQUID BANDAGE?
Yes. 5 FDA drug label records list LIQUID BANDAGE 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 Benzethonium chloride and Dyclonine hydrochloride 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.