MyDerm Bite and Sting

MyDerm Bite and Sting is an FDA-registered drug product whose active ingredient is BENZOCAINE. It is labelled by Medline Industries taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 53329-038, application M017, label effective 20260526. It is one of 70 FDA drug label records sharing the active ingredient BENZOCAINE. 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 BENZOCAINE are most often described in connection with: temporary relief, itching associated, insect bites. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Temporary relief of pain and itching associated with insect bites

Direction Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a physician

For external use only When using this product • avoid contact with the eye

FDA lists 70 drug label records with BENZOCAINE 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.

5 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 MyDerm Bite and Sting used for?
Temporary relief of pain and itching associated with insect bites

Who makes MyDerm Bite and Sting?
Medline Industries is the labeler of record for MyDerm Bite and Sting. 70 FDA label records share the active ingredient BENZOCAINE, 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 MyDerm Bite and Sting 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 MyDerm Bite and Sting 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 BENZOCAINE?
Yes. 70 FDA drug label records list BENZOCAINE 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 MyDerm Bite and Sting been recalled?
5 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.