Meridian Unwrapped antibacterial deodorant

Meridian Unwrapped antibacterial deodorant is an FDA-registered drug product whose active ingredient is BENZETHONIUM CHLORIDE. It is labelled by Bob Barker Company Inc. taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 53247-142, application M003, label effective 20260729. It is one of 15 FDA drug label records sharing the active ingredient BENZETHONIUM 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 BENZETHONIUM CHLORIDE are most often described in connection with: washing decrease, bacteria skin. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For washing to decrease bacteria on skin.

Directions Wet bar with water. Lather vigorously and wash skin. Rinse and dry thoroughly.

Caution For external use only. Do not use this product on infants under 6. When using this product avoid contact with eyes. In case of eye contact, flush with water. Stop use and consult doctor if irritation and rash develops. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

FDA lists 15 drug label records with BENZETHONIUM 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 Meridian Unwrapped antibacterial deodorant used for?
Uses For washing to decrease bacteria on skin.

Who makes Meridian Unwrapped antibacterial deodorant?
Bob Barker Company Inc. is the labeler of record for Meridian Unwrapped antibacterial deodorant. 15 FDA label records share the active ingredient BENZETHONIUM 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 Meridian Unwrapped antibacterial deodorant come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Meridian Unwrapped antibacterial deodorant 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 BENZETHONIUM CHLORIDE?
Yes. 15 FDA drug label records list BENZETHONIUM 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 Meridian Unwrapped antibacterial deodorant 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.