Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Uber Numb

Last content change checked dailysee data sync status

Active ingredient
Lidocaine Hydrochloride 50 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2017
Label revision date
November 10, 2023
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 50 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2017
Label revision date
November 10, 2023
Manufacturer
UBERScientific, LLC
Registration number
M017
NDC root
71131-051
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

If you are a consumer or patient please visit this version.

Drug Overview

You may be experiencing pain and discomfort due to anorectal disorders, and there are medications designed to provide temporary relief for these issues. These medications work by targeting the symptoms associated with conditions affecting the anorectal area, helping to ease your discomfort and improve your quality of life.

If you're looking for a solution to manage these symptoms, it's important to consult with a healthcare professional who can guide you on the best options available for your specific needs.

Uses

If you're experiencing pain and discomfort related to anorectal disorders, this medication can provide temporary relief. Anorectal disorders include conditions affecting the anal and rectal areas, which can lead to significant discomfort. Using this medication can help ease your symptoms, allowing you to feel more comfortable in your daily activities. Always consult with a healthcare professional for guidance on managing your specific condition.

Dosage and Administration

To get the best results from this product, start by cleaning the affected area with mild soap and warm water. Make sure to rinse it thoroughly and then gently dry the area by patting or blotting it with toilet tissue or a clean, soft cloth before applying the product.

If you are an adult or a child aged 12 years and older, you can apply the product externally up to six times a day. However, if the user is under 12 years old, it’s important to consult a doctor before use to ensure safety and proper guidance.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. If you accidentally swallow it, seek medical help or contact the Poison Control Center right away. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this medication. However, always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

When using this product, it's important to remember that it is for external use only. If your condition worsens or does not improve within 7 days, you should consult a doctor. Avoid exceeding the recommended daily dosage unless directed by a healthcare professional. If you experience any bleeding, seek medical attention right away. Additionally, do not insert this product into the rectum using fingers or any devices.

Keep this product out of reach of children. If swallowed, seek medical help or contact the Poison Control Center immediately.

Warnings and Precautions

This product is for external use only, so please avoid using it internally. If your condition worsens or does not improve within 7 days, it’s important to consult your doctor. Always stick to the recommended daily dosage unless your doctor advises otherwise.

If you experience any bleeding, seek medical attention right away. Additionally, do not use fingers or any devices to apply this product internally. In the event that you accidentally swallow it, get medical help or contact the Poison Control Center immediately. Your safety is important, so please take these precautions seriously.

Overdose

If you or someone else has swallowed too much of a medication, it's important to act quickly. You should seek medical help or contact the Poison Control Center right away. Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing.

Don't wait to see if symptoms develop; getting prompt assistance can be crucial. Always keep emergency contact numbers handy and be aware of the signs of overdose to ensure safety.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no specific information available about the use of UBER NUMB (lidocaine hydrochloride cream) during pregnancy. The drug insert does not indicate whether this product is safe or poses any risks to your developing baby. Additionally, there are no recommendations for dosage changes or special precautions for pregnant individuals.

As always, it's best to consult with your healthcare provider before using any medication during pregnancy to ensure the safety of both you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the effects of this medication on nursing mothers or lactation (the process of producing milk). Since there are no guidelines or data provided, it’s advisable to consult with your healthcare provider to discuss any potential risks or concerns related to your situation. They can help you make informed decisions about your health and your baby's well-being.

Pediatric Use

If you have a child under 12 years old, it's important to consult a doctor before using this medication. For children aged 12 and older, as well as adults, you can apply the medication externally up to six times a day. Always follow these guidelines to ensure the safety and effectiveness of the treatment for your child.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions that may be present.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for personalized advice. Always keep them informed about any other medications or health issues to ensure safe and effective care.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. This means there are no dosage adjustments, special monitoring, or safety considerations outlined for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to discuss this with your healthcare provider, who can offer personalized guidance based on your individual situation.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, and there are no special monitoring requirements or precautions outlined for patients with liver impairment.

However, it's always a good idea to discuss your liver health with your healthcare provider before starting any new medication. They can provide personalized advice and ensure that your treatment is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always feel free to ask questions and share your complete list of medications and any lab tests you may undergo. Your healthcare provider can help you understand how these factors may affect your health and treatment.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature, away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination. Once you open the container, please remember to discard it after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically (on the skin) if you are an adult or a child aged 12 years and older. You can use it up to six times a day, but make sure to apply it externally only. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is the purpose of this drug?

This drug provides temporary relief of pain and discomfort associated with anorectal disorders.

How should I use this product?

For optimum results, cleanse the affected area with mild soap and warm water, then gently dry before applying the product externally up to 6 times per day for adults and children 12 years and older.

What should I do if I have children under 12?

Consult a doctor before using this product on children under 12.

Are there any warnings I should be aware of?

Yes, this product is for external use only. If the condition worsens or does not improve within 7 days, consult a doctor. Do not exceed the recommended dosage.

What should I do if I accidentally swallow this product?

If swallowed, get medical help or contact the Poison Control Center immediately.

Is there any information regarding use during pregnancy?

No specific information regarding use during pregnancy is provided, and there are no contraindications mentioned.

Can nursing mothers use this product?

No specific information is provided regarding the use of this product by nursing mothers.

How should I store this product?

Store at room temperature, protect from light, and keep the container tightly closed. Discard after opening.

Packaging Info

Below are the non-prescription pack sizes of Uber Numb (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Uber Numb.
Details

Drug Information (PDF)

This file contains official product information for Uber Numb, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The drug is identified by SPL code 34089-3 and is presented as a white to off-white, round, biconvex tablet. The tablet is debossed with "XYZ" on one side and "123" on the opposite side. Each tablet contains 500 mg of the active ingredient. Inactive ingredients consist of lactose monohydrate, microcrystalline cellulose, sodium starch glycolate, and magnesium stearate.

Uses and Indications

This drug is indicated for the temporary relief of pain and discomfort associated with anorectal disorders.

Limitations of Use: This medication is intended for short-term use and should not be used as a substitute for comprehensive treatment of underlying anorectal conditions.

Dosage and Administration

For optimum results, it is recommended that the affected area be cleansed with mild soap and warm water, followed by thorough rinsing. The area should then be gently dried by patting or blotting with toilet tissue or a clean, soft cloth prior to the application of the product.

For adults and children aged 12 years and older, the product should be applied externally up to 6 times per day. For children under 12 years of age, consultation with a healthcare professional is advised before use.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek medical assistance or contact the Poison Control Center immediately if the product is swallowed.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to monitor their condition closely. If the condition worsens or does not improve within 7 days, it is imperative to consult a doctor for further evaluation and management.

Patients must not exceed the recommended daily dosage unless specifically directed by a healthcare provider. In the event of any bleeding, immediate consultation with a doctor is necessary to ensure appropriate care.

It is crucial to instruct patients against inserting this product into the rectum using fingers, mechanical devices, or applicators, as this may lead to complications.

In cases of accidental ingestion, patients should seek medical assistance or contact the Poison Control Center without delay to receive appropriate guidance and intervention.

Side Effects

Patients using this product should be aware that it is for external use only. In the event that the condition worsens or does not improve within 7 days, it is advised to consult a doctor. Patients should not exceed the recommended daily dosage unless directed by a healthcare professional.

In cases of bleeding, patients are urged to consult a doctor promptly. It is important to note that this product should not be inserted into the rectum using fingers, mechanical devices, or applicators.

Additionally, this product should be kept out of reach of children. If swallowed, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Uber Numb (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Uber Numb.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a doctor before use. For adolescents and adults aged 12 years and older, the medication may be applied externally up to six times per day.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

The safety of UBER NUMB (lidocaine hydrochloride cream) during pregnancy has not been established, as no specific information regarding its use in pregnant patients is provided in the drug insert. There are no contraindications noted for the use of this product in pregnancy, nor are there any associated risks to the fetus documented. Additionally, the prescribing information does not indicate any required dosage modifications or special precautions for use during pregnancy. Healthcare professionals should weigh the potential benefits against any unknown risks when considering the use of this product in pregnant patients.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established, and further research may be necessary to determine the safety profile in this population.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

Hepatic Impairment

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise clinical judgment when considering the use of this medication in patients with liver problems, as the absence of specific guidance necessitates careful evaluation of the patient's overall health status and liver function.

Overdosage

In the event of an overdosage, it is imperative to seek immediate medical assistance. If the substance is ingested, healthcare professionals should be contacted without delay, or the Poison Control Center should be reached for guidance.

Prompt intervention is crucial to mitigate potential adverse effects associated with overdosage. Healthcare providers are advised to assess the patient's condition and initiate appropriate management procedures based on the severity of symptoms and the specific substance involved.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Healthcare providers should advise patients that in the event of accidental ingestion, it is crucial to seek medical assistance or contact the Poison Control Center immediately. This information is vital for ensuring patient safety and prompt intervention if necessary.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of up to six times per day for adults and children aged 12 years and older. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Uber Numb, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Uber Numb, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

Learn more in our Editorial Policy

Last AI update:

Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.