Sign In

Save up to 80% by drug discount in your pharmacy with "Pharmacy Near Me - National Drug Discount Card"

You can scan QR Code(just open camera on your phone/scan by application) from the image on prescription drug discount card to save it to your mobile phone. Or just click on image if you're on mobile phone.

View Generic:
View Brand:

Uber numb - Medication Information

Product NDC Code 71131-050
Drug Name

Uber numb

Type Brand
Pharm Class Amide Local Anesthetic [EPC],
Amides [CS],
Antiarrhythmic [EPC],
Local Anesthesia [PE]
Active Ingredients
Lidocaine hydrochloride 50 mg/ml
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1545290
Application Number M017
Labeler Name UBERScientific, LLC
Packages
Package NDC Code Description
71131-050-04 118.29 ml in 1 bottle, spray (71131-050-04)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredients Lidocaine HCL 5% Purpose Topical Anesthetic

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
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

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Purified Water, Propylene Glycol, Sodium Metabisulfite, Citric Acid, Epinephrine HCL, Diazolidinyl Urea, Methyl Paraben, Propyl Paraben, and Disodium EDTA.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses Temporarily relieves pain, itching or swelling associated with anorectal disorders. External Use Only.

Purpose

Information about the drug product’s indications for use.
Purpose Topical Anesthetic

Spl product data elements

Usually a list of ingredients in a drug product.
Uber Numb LIDOCAINE HYDROCHLORIDE WATER PROPYLENE GLYCOL SODIUM METABISULFITE CITRIC ACID MONOHYDRATE EPINEPHRINE HYDROCHLORIDE DIAZOLIDINYL UREA METHYLPARABEN PROPYLPARABEN EDETATE DISODIUM ANHYDROUS LIDOCAINE HYDROCHLORIDE LIDOCAINE LIDOCAINE

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
Package Labeling: Label

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Drug Facts Distributed by: UberScientific TM 838 E High St. Ste 271 Lexington, KY 40502 302 566 -8237

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
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.

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
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.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
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.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API