NumbMD Lidocaine Cream Anorectal(hemorrhoidal)

NumbMD Lidocaine Cream Anorectal(hemorrhoidal) is an FDA-registered drug product whose active ingredient is LIDOCAINE 5%. It is labelled by EveryMarket Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 85833-006, application M015, label effective 20260812. 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: practical cleanse, theaffected area, mild soap, warm water, andrinse thoroughly, gently dry, bypatting blotting, toilet tissue. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Adults: When practical, cleanse theaffected area with mild soap and warm water andrinse thoroughly. Gently dry bypatting or blotting with toilet tissue or a soft cloth before application of this product. Apply to the affected area up to 6 times daily. Children under 12 years of age:consult a doctor.

For the temporary relief of local itching and discomfort associated with anorectal disorders. For the temporary relief of pain, burning and soreness.

For external use only If condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended dailydosage, unless directed by a doctor. in case of bleeding, consult a doctor promptly. Do not put this product into the rectum byusing fingers or any mechanical device or applicator. an llergic reaction occurs. symptom does not improve or if redness, irritation, swelling, pain or other symptom developor increase. ask a health professional before use. In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away. (1-800-222-1222)

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.

What is NumbMD Lidocaine Cream Anorectal(hemorrhoidal) used for?
Adults: When practical, cleanse theaffected area with mild soap and warm water andrinse thoroughly. Gently dry bypatting or blotting with toilet tissue or a soft cloth before application of this product. Apply to the affected area up to 6 times daily. Children under 12 years of age:consult a doctor.

Who makes NumbMD Lidocaine Cream Anorectal(hemorrhoidal)?
EveryMarket Inc is the labeler of record for NumbMD Lidocaine Cream Anorectal(hemorrhoidal). 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 NumbMD Lidocaine Cream Anorectal(hemorrhoidal) 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 NumbMD Lidocaine Cream Anorectal(hemorrhoidal) 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 NumbMD Lidocaine Cream Anorectal(hemorrhoidal) 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.