MEDI-FIRST

MEDI-FIRST is an FDA-registered drug product whose active ingredient is BENZALKONIUM CHLORIDE, LIDOCAINE. It is labelled by Orazen Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71927-019, application M017, label effective 20260905. It is one of 4 FDA drug label records sharing the active ingredient BENZALKONIUM CHLORIDE, LIDOCAINE. 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, LIDOCAINE are most often described in connection with: temporary relief, pain associated, minor burns, helps protect, against harmful. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses for the temporary relief of pain associated with minor burns helps protect against harmful bacteria

Directions Adults and children 2 years and over: clean the affected area, apply a small amount not more than 3 to 4 times daily Children under 2 years: do not use, consult a doctor

Warnings For external use only.

FDA lists 4 drug label records with BENZALKONIUM CHLORIDE, LIDOCAINE 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.

2 FDA recall record(s) match this product name or manufacturer. A match means the firm or product name appears in the enforcement report; confirm lot numbers and dates against the official FDA notice before acting.

What is MEDI-FIRST used for?
Uses for the temporary relief of pain associated with minor burns helps protect against harmful bacteria

Who makes MEDI-FIRST?
Orazen Inc is the labeler of record for MEDI-FIRST. 4 FDA label records share the active ingredient BENZALKONIUM CHLORIDE, LIDOCAINE, 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 MEDI-FIRST 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 MEDI-FIRST 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, LIDOCAINE?
Yes. 4 FDA drug label records list BENZALKONIUM CHLORIDE, LIDOCAINE 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 MEDI-FIRST been recalled?
2 FDA recall record(s) match this product name or manufacturer. Review the recall and safety notices section on this page and confirm lot numbers against the official FDA enforcement report.

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.