Lidoxi

Lidoxi is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by T&T Pharma Holdings LLC taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 87239-1111, application M017, label effective 20260507. 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: temporary relief, muscle pain, backache cramps, soreness strains, discomfort neckache. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of muscle pain and joint pain associated with: -Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Directions: Adults and Children 12 Years of Age and Older - Clean and dry the affected area before treatment - Apply up to 4 times daily - Wash hands immediately after use

Warnings: For External Use Only Allergy Alert Local anesthetics may cause methemoglobinemia. If an allergic reaction occurs, stop use and seek medical attention immediately. Do Not Use - On damaged, irritated, or infected skin - With a bandage or heating pad - If you are allergic to any ingredients in this product - In the eyes, nose, or mouth - Otherwise as directed When Using This Product Avoid contact with the eyes, nose, and mouth Stop Use and Ask Doctor If - Any of the Warnings apply to you - Excessive skin irritation develops - Condition worsens - Symptoms persist for more than 7 days, or symptoms clear up and occur aqain within 3 days If Pregnant or Breast-feeding Ask a healthcare professional before use Keep Out of Reach of Children If ingested seek medical help or contact a Poison Control Center immediately Flammable Keep away from excessive heat or open flame

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.

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 Lidoxi used for?
Uses For the temporary relief of muscle pain and joint pain associated with: -Backache -Cramps -Soreness -Strains -Discomfort -Neckache

Who makes Lidoxi?
T&T Pharma Holdings LLC is the labeler of record for Lidoxi. 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 Lidoxi come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Lidoxi 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 Lidoxi 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.