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Uber Numb Topical Anesthetic

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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 2016
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 2016
Label revision date
November 10, 2023
Manufacturer
UberScientific, LLC
Registration number
M015
NDC root
71131-774
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

This medication is designed to provide temporary relief from local pain and discomfort associated with anorectal disorders, which are conditions affecting the area around the anus and rectum. If you are experiencing discomfort in this area, this drug may help alleviate your symptoms and improve your comfort.

Uses

If you're experiencing local pain and discomfort due to anorectal disorders, this medication can provide temporary relief. Anorectal disorders include conditions affecting the area around the anus and rectum, which can cause significant discomfort. By using this medication, you can help ease those symptoms and improve your comfort. Always consult with a healthcare professional for advice tailored to your specific situation.

Dosage and Administration

To use this medication, start by applying it directly to the area that needs treatment. If you are an adult or a child aged 12 years and older, you can apply it externally up to six times a day. However, if the patient is under 12 years old, it’s important to consult a physician (doctor) before using the medication.

Before applying, make sure to clean the affected area with warm water and mild soap, then rinse it thoroughly. After cleaning, gently dry the area by patting it with toilet tissue or a soft cloth. This preparation helps ensure the medication works effectively.

What to Avoid

It's important to use this product safely and effectively. You should never insert it into the rectum using your fingers or any mechanical device. Additionally, be cautious and stop using the product if your symptoms worsen or do not improve within seven days, if you experience any bleeding, or if you notice redness, irritation, swelling, pain, or other concerning symptoms.

When using this product, make sure not to exceed the recommended daily dosage unless your doctor advises you to do so. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

When using this product, it's important to follow the directions carefully. You should not exceed the recommended daily dosage unless your doctor advises you to do so. This product is for external use only, and you should avoid inserting it into the rectum with your fingers or any device.

If you notice that your symptoms worsen or do not improve within seven days, or if you experience any bleeding, redness, irritation, swelling, pain, or other concerning symptoms, stop using the product immediately. Additionally, keep this product out of reach of children, and consult a physician if a child under 12 needs to use it.

Warnings and Precautions

This product is for external use only, so be sure to follow the directions provided. It's important not to exceed the recommended daily dosage unless your doctor advises you to do so. Avoid inserting this product into the rectum with your fingers or any device. Keep it out of reach of children, and if your child is under 12, consult a physician before use.

You should stop using this product and call your doctor if your symptoms worsen or do not improve within seven days. Additionally, seek medical attention if you experience any bleeding, or if you notice redness, irritation, swelling, pain, or other concerning symptoms.

Overdose

Taking more than the recommended daily dosage of your medication can lead to serious health risks. It's important to follow your doctor's instructions carefully and not exceed the dosage unless specifically advised by them.

If you suspect an overdose, look for signs such as unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, seek immediate medical help. Always prioritize your safety and consult a healthcare professional if you have any concerns about your medication.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of lidocaine hydrochloride cream during pregnancy has not been established. In fact, using this product is not recommended due to potential risks to your developing baby. Before considering its use, you should consult with your physician to discuss any concerns and to ensure it is safe for you.

Additionally, if you do receive approval to use this cream, be aware that dosage adjustments may be necessary. Always seek guidance from your healthcare provider to determine the appropriate dosage for your situation. Your health and the health of your baby are the top priority, so make sure to have open conversations with your doctor about any medications you are considering.

Lactation Use

If you are a nursing mother, you can use Uber Numb Topical Anesthetic without specific warnings or recommendations against it. Currently, there are no known concerns about this medication being passed into breast milk or any associated risks for your infant.

As always, it's a good idea to consult with your healthcare provider if you have any questions or concerns about using medications while breastfeeding.

Pediatric Use

If you are considering using this medication for your child, it's important to know that children under 12 should consult a physician (doctor) before use. For both adults and children aged 12 and older, it's also recommended to speak with a physician prior to using the medication.

When applying the medication, you can do so externally to the affected area up to six times a day. Always follow your healthcare provider's guidance to ensure safe and effective use 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. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no guidelines, dosage adjustments, or monitoring instructions to share 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 for personalized advice and recommendations.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This way, you can work together to ensure your treatment is safe and effective.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, away from direct sunlight. This helps maintain its effectiveness and safety.

When handling the product, be sure to keep it in a clean environment to avoid contamination. Following these simple storage and handling guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically, meaning you will put it directly on the skin. You can use it up to six times a day on the affected area. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is the purpose of this drug?

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

How should I apply this product?

Clean the affected area with warm water and mild soap, rinse thoroughly, and gently dry by patting with toilet tissue or a soft cloth. Apply externally to the area up to six times per day.

What should I do if symptoms worsen?

Stop using the product if symptoms worsen or do not improve within seven days, or if bleeding, redness, irritation, swelling, or pain occurs.

Is this product safe for children?

Children under 12 should consult a physician before use. Adults and children 12 years and over can use it, but should consult a physician if needed.

Can I use this product during pregnancy?

The safety of this product during pregnancy has not been established, and its use is contraindicated due to potential risks to the fetus. Consult a physician if pregnant or planning to become pregnant.

What precautions should I take when using this product?

Use only as directed for external use only. Do not exceed the recommended daily dosage, and do not insert the product into the rectum using fingers or any mechanical device.

How should I store this product?

Store at room temperature and avoid direct sunlight.

Packaging Info

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

Packaging configurations for Uber Numb Topical Anesthetic.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the temporary relief of local 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

The medication should be applied externally to the affected area. For adults and children aged 12 years and older, the recommended application frequency is up to six times per day. It is advised that healthcare professionals consult a physician prior to use for children under 12 years of age.

To ensure proper application, the affected area must first be cleaned with warm water and mild soap, followed by thorough rinsing. After cleansing, the area should be gently dried by patting with toilet tissue or a soft cloth.

Contraindications

The use of this product is contraindicated in patients who intend to insert it into the rectum using fingers or any mechanical device, as this may lead to complications.

Additionally, the product should be discontinued if symptoms worsen or do not improve within seven days, or if any bleeding occurs, along with the development of redness, irritation, swelling, pain, or other concerning symptoms.

Healthcare professionals should advise patients not to exceed the recommended daily dosage unless directed by a physician.

Warnings and Precautions

For external use only, this product should be applied strictly as directed. Healthcare professionals must advise patients not to exceed the recommended daily dosage unless specifically instructed by a physician.

It is imperative that patients are cautioned against inserting this product into the rectum using fingers or any mechanical device, as this may lead to adverse effects.

To ensure safety, this product must be kept out of reach of children. It is recommended that children under the age of 12 consult a physician prior to use to mitigate any potential risks.

Patients should be instructed to discontinue use and seek medical advice if any of the following occur: symptoms worsen or do not improve within seven days, or if bleeding, redness, irritation, swelling, pain, or any other concerning symptoms develop. Monitoring for these adverse reactions is essential to ensure patient safety and effective treatment outcomes.

Side Effects

Patients using this product should be aware that it is intended for external use only and must be used strictly as directed. Exceeding the recommended daily dosage without medical advice is not advised.

Participants should refrain from inserting this product into the rectum using fingers or any mechanical device, as this may lead to adverse effects. It is crucial to keep the product out of reach of children, and those under the age of 12 should consult a physician prior to use.

Patients are advised to discontinue use and seek medical attention if symptoms worsen or do not improve within seven days. Additionally, if any bleeding occurs, or if redness, irritation, swelling, pain, or other concerning symptoms develop, the use of this product should be stopped immediately.

Drug Interactions

There are no specific drug interactions or laboratory test interactions identified in the available data. Therefore, no recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Uber Numb Topical Anesthetic.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a physician prior to use. For adolescents aged 12 years and older, it is also recommended to consult a physician before use. The product is intended for external application to the affected area, with a maximum frequency of up to six times per day.

Geriatric Use

There is no specific information available regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

The safety of lidocaine hydrochloride cream during pregnancy has not been established. Use of this product is contraindicated in pregnancy due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a physician before using this product. Additionally, dosage adjustments may be necessary for pregnant individuals; therefore, it is advisable to consult a healthcare provider for guidance on appropriate use.

Lactation

There are no specific warnings or recommendations regarding the use of Uber Numb Topical Anesthetic in lactating mothers. Additionally, there are no statements concerning the potential for excretion of the drug in breast milk or any associated risks to breastfed infants.

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

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions for individuals with compromised liver function. It is recommended that healthcare providers exercise caution when prescribing this medication to patients with hepatic impairment, given the lack of data on its safety and efficacy in this population. Regular monitoring of liver function may be warranted based on clinical judgment.

Overdosage

Overdosage of the medication can lead to serious health consequences. It is imperative that healthcare professionals adhere to the recommended daily dosage guidelines to mitigate the risk of overdosage.

In the event of suspected overdosage, immediate medical attention should be sought. Symptoms of overdosage may vary depending on the specific medication and the extent of the overdose. Healthcare providers should be vigilant in monitoring patients for any adverse effects that may arise.

Management of overdosage typically involves supportive care and symptomatic treatment. Healthcare professionals are advised to consult the relevant clinical guidelines and toxicology resources for specific management protocols tailored to the medication in question.

It is crucial to emphasize that patients should not exceed the recommended daily dosage unless explicitly directed by a qualified healthcare provider. This precaution is essential to ensure patient safety and to prevent the potential complications associated with overdosage.

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 use of the compound in these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients that children under the age of 12 must consult a physician prior to using this product. It is important to emphasize that patients should not insert this product into the rectum using fingers or any mechanical device, as this could lead to complications.

Patients should be instructed to discontinue use of the product if symptoms worsen or do not improve within seven days. Additionally, they should stop using the product if any bleeding occurs or if they experience redness, irritation, swelling, pain, or any other concerning symptoms.

Furthermore, healthcare providers should remind patients not to exceed the recommended daily dosage unless specifically directed by a doctor, as adherence to dosing guidelines is crucial for safety and efficacy.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at room temperature, ensuring that it is kept away from direct sunlight to maintain its integrity and effectiveness. Proper handling should be observed to prevent exposure to conditions that may compromise the quality of the product.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of up to six times per day to the affected area. 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 Topical Anesthetic, 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 Topical Anesthetic, 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.