Lidocaine Roll-on

Lidocaine Roll-on is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by YYBA Corp taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 73581-023, application M015, label effective 20260527. 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 relieve, local itching, perianal area, temporary relief, pain irritation, burning temporarily, shrinks hemorrhoidal. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Helps relieve local itching and discomfort in the perianal area For the temporary relief of pain, irritation or burning Temporarily shrinks hemorrhoidal tissue

Directions Adults: When practical, cleanse the affected area with mild soap and warm water and rinse by patting or blotting with an appropriate cleansing pad. Gently dry by patting or blotting with toilet tissue or a soft cloth before application of this product. Apply externally to the affected area up to 6 times daily or after each bowel movement. Children under 12 years of age: consult a doctor.

Warnings For external use only Do not exceed the recommended daily dosage unless directed by a doctor. Do not put this product into the rectum by using your fingers or any mechanical device or applicator. Do not use this product if you have heart disease, high blood pressure, thyroid disease, diabetes, or difficulty in urination due to enlargement of the prostate gland unless directed by a doctor. When using this product if the condition worsens or does not improve within 7 days, consult a doctor. In case of bleeding, consult a doctor promptly. Stop use and ask a doctor if the symptoms being treated do not subside or if redness, irritation, swelling, pain, or other symptoms develop or increase. Ask a doctor or pharmacist before use if you are presently taking a prescription drug for high blood pressure or depression. Allergy alert: Certain persons can develop allergic reactions to ingredients in this product.

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 Lidocaine Roll-on used for?
Uses Helps relieve local itching and discomfort in the perianal area For the temporary relief of pain, irritation or burning Temporarily shrinks hemorrhoidal tissue

Who makes Lidocaine Roll-on?
YYBA Corp is the labeler of record for Lidocaine Roll-on. 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 Lidocaine Roll-on 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 Lidocaine Roll-on 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 Lidocaine Roll-on 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.