Prolayed Lidocaine Male Genital Desensitizer

Prolayed Lidocaine Male Genital Desensitizer is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by ViaDerma Distribution, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71262-006, application M017, label effective 20231202. It is one of 152 FDA drug label records sharing the active ingredient 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 LIDOCAINE are most often described in connection with: helps temporarily, onset ejaculation. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Use Helps in temporarily slowing the onset of ejaculation.

Directions Apply 3 or more sprays, not to exceed 10, to head and shaft of penis before intercourse, or use as directed by a doctor. Wash product off after intercourse.

Warnings For external use only When using this product avoid contact with the eyes. Stop use and ask a doctor if this product, used as directed, does not provide relief. Premature ejaculation may be due to a condition requiring medical supervision you or your partner develop a rash or irritation, such as burning or itching. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

FDA lists 152 drug label records with 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.

What is Prolayed Lidocaine Male Genital Desensitizer used for?
Use Helps in temporarily slowing the onset of ejaculation.

Who makes Prolayed Lidocaine Male Genital Desensitizer?
ViaDerma Distribution, Inc. is the labeler of record for Prolayed Lidocaine Male Genital Desensitizer. 152 FDA label records share the active ingredient 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 Prolayed Lidocaine Male Genital Desensitizer 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 Prolayed Lidocaine Male Genital Desensitizer 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?
Yes. 152 FDA drug label records list 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 Prolayed Lidocaine Male Genital Desensitizer 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.