Uber Numb Topical Anesthetic
Uber Numb Topical Anesthetic is an FDA drug label for the active ingredient LIDOCAINE HYDROCHLORIDE manufactured by UberScientific, LLC administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231110.
- Generic name
- LIDOCAINE HYDROCHLORIDE
- Manufacturer
- UberScientific, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 71131-774
- Application
- M015
- Label effective
- 20231110
About this product
Uber Numb Topical Anesthetic 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 71131-774, application M015, 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.
What it is used for
Across FDA labelling, products containing LIDOCAINE HYDROCHLORIDE are most often described in connection with: temporary relief, local pain, discomfort associated, anorectal disorders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses: For the temporary relief of local pain and discomfort associated with anorectal disorders.
Dosage & Administration
Directions: apply to affected area. Adults and children 12-years and over: consult a physician before use. Children under 12, How to Apply: Clean affected area with warm water nad mild soap. Rinse thoroughly. Gently dry by patting with toilet tissue or soft cloth. Apply externally to area up to six times per day.
Warnings
Warnings: For external use only. Use only as directed. When using this product, do not exceed the recommended daily dosage unless directed by a doctor. Do not insert this product into rectum using fingers or any mechanical device. Keep out of reach of children. Children under 12 should consult physician prior to use. Stop using this product if: Symptoms worsen or does not improve within seven days Bleeding occurs. Redness, irritation, swelling, pain or other symptoms develop.
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View labelHow products containing LIDOCAINE HYDROCHLORIDE compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Medical Purchasing Solutions, LLC | 18 |
| — | — | Asclemed USA, Inc. | 6 |
| — | — | Water-Jel Technologies | 6 |
| — | — | SKINS SEXUAL HEALTH LIMITED | 5 |
| — | — | Nantong Health & Beyond Hygienic Products Inc. | 4 |
Frequently asked questions
What is Uber Numb Topical Anesthetic used for?
Uses: For the temporary relief of local pain and discomfort associated with anorectal disorders.
Who makes Uber Numb Topical Anesthetic?
UberScientific, LLC is the labeler of record for Uber Numb Topical Anesthetic. 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 Topical Anesthetic 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 Topical Anesthetic 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 Topical Anesthetic 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.