Uber Numb

Uber Numb is an FDA-registered drug product whose active ingredient is LIDOCAINE HYDROCHLORIDE. It is labelled by UBERScientific, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71131-050, application M017, label effective 20231110. It is one of 110 FDA drug label records sharing the active ingredient LIDOCAINE HYDROCHLORIDE. 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 HYDROCHLORIDE are most often described in connection with: temporarily relieves, pain itching, swelling associated, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Temporarily relieves pain, itching or swelling associated with anorectal disorders. External Use Only.

Directions: Prior to using therapeutically, test on small area of skin for sensitivities and possible allergies, if adverse reaction occurs seek medical attention. Spray UberNumb anesthetic spray, sparingly, on affected area. The Area should begin to feel numbing anestehetic relief within two minutes. For continued numbing releif, reapply UberNumb sparingly as needed. If at any point, irritations or other sensitivities occur, discontinue use and seek medical attention Store in a cool dark place or refrigerate. Discard after expiration date

Warnings: Keep out of reach of children. Do not use if pregnant or breast feeding. For external use only, if accidentally ingested, seek meical attention immediately. Do not use in large quantities, particularly over raw surfaces or blistered areas. Avoid contact with the eyes, if contact with the eyes occur, rinse with copious amounts of eyewash and seek medical attention immediately. Use on small area of skin to test for sensitivities prior to use. Do not Use if: you have a history of seizures. you have been diagnosed with liver disease. you have an allergy to any of the ingredients listed. If a reaction or sensitivity occurs, discontinue use and seek medical attention immediately. If condition worsens or symptoms are persistent for more than five days, or recur after clearing up, consult with a medical professional immediately.

FDA lists 110 drug label records with LIDOCAINE HYDROCHLORIDE 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 Uber Numb used for?
Uses Temporarily relieves pain, itching or swelling associated with anorectal disorders. External Use Only.

Who makes Uber Numb?
UBERScientific, LLC is the labeler of record for Uber Numb. 110 FDA label records share the active ingredient LIDOCAINE HYDROCHLORIDE, 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 Uber Numb 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 Uber Numb 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 HYDROCHLORIDE?
Yes. 110 FDA drug label records list LIDOCAINE HYDROCHLORIDE 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 Uber Numb 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.