Oxify

Oxify is an FDA-registered drug product whose active ingredient is LIDOCAINE 5%. It is labelled by Weeks & Leo Compnay, INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 11383-003, application M015, label effective 20260514. It is one of 13 FDA drug label records sharing the active ingredient LIDOCAINE 5%. 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 LIDOCAINE 5% are most often described in connection with: helps relieve, pain itching, burning associated, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Helps relieve the pain, itching, and burning associated with hemorrhoids and other anorectal disorders

when practical, clean area with mild soap and warm water and rinse thoroughly. Gently dry by patting or blotting with toiled tissue or soft cloth before applying adults and children 12 years and over: apply externally to the affected area up to 6 times a day children under 12 years: consult a doctor

For External use only

FDA lists 13 drug label records with LIDOCAINE 5% 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.

1 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 Oxify used for?
Helps relieve the pain, itching, and burning associated with hemorrhoids and other anorectal disorders

Who makes Oxify?
Weeks & Leo Compnay, INC. is the labeler of record for Oxify. 13 FDA label records share the active ingredient LIDOCAINE 5%, 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 Oxify 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 Oxify 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 LIDOCAINE 5%?
Yes. 13 FDA drug label records list LIDOCAINE 5% 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 Oxify been recalled?
1 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.