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Uber Numb

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Active ingredient
Lidocaine Hydrochloride 50 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Liquid
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 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Liquid
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
71131-050
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 temporarily relieve pain, itching, or swelling associated with anorectal disorders, which are conditions affecting the area around the anus and rectum. It is important to note that this product is for external use only, meaning it should not be applied internally. If you are experiencing discomfort in this area, this medication may help provide some relief.

Uses

If you're dealing with discomfort from anorectal disorders, this medication can help. It temporarily relieves pain, itching, or swelling in that area, providing you with some much-needed relief.

Remember, this product is for external use only, so be sure to apply it as directed to avoid any complications.

Dosage and Administration

Before you start using UberNumb anesthetic spray, it's important to test it on a small area of your skin to check for any sensitivities or allergies. Once you've done that, you can spray the anesthetic sparingly on the area that needs relief. You should start to feel a numbing effect within about two minutes.

If you need more numbing relief, you can reapply the spray as needed, but remember to use it sparingly. If you experience any irritation or other sensitivities while using the spray, stop using it immediately and seek medical attention. Your safety and comfort are the top priority!

What to Avoid

You should avoid using this product if you are pregnant or breastfeeding, have a history of seizures, have been diagnosed with liver disease, or are allergic to any of the ingredients. It's important to use this product carefully; do not apply it in large quantities, especially on raw or blistered skin.

Make sure to keep it away from your eyes—if contact occurs, rinse thoroughly with eyewash and seek medical help right away. Before applying it to a larger area, test it on a small patch of skin to check for any sensitivities. If you experience any adverse reactions or if your condition worsens or persists for more than five days, consult a healthcare professional immediately.

Side Effects

You should be aware of some important side effects and warnings associated with this product. It is not safe to use if you are pregnant or breastfeeding, and it is intended for external use only. If ingested accidentally, seek medical help right away. Avoid applying it in large amounts, especially on raw or blistered skin, and keep it away from your eyes. If it does come into contact with your eyes, rinse thoroughly and seek medical attention.

Additionally, do not use this product if you have a history of seizures, liver disease, or allergies to any of its ingredients. If you experience any reactions or sensitivities, stop using it immediately and consult a healthcare professional, especially if your symptoms persist for more than five days or return after improvement. Always test a small area of skin for sensitivity before full use.

Warnings and Precautions

You should not use this product if you are pregnant or breastfeeding. It is meant for external use only, so if you accidentally swallow it, seek medical help right away. Avoid applying it in large amounts, especially on raw or blistered skin, and keep it away from your eyes. If it does get in your eyes, rinse them thoroughly with eyewash and get medical attention immediately. Before using it on a larger area, test it on a small patch of skin to check for any sensitivities.

Do not use this product if you have a history of seizures, liver disease, or if you are allergic to any of its ingredients. If you experience any reactions or sensitivities, stop using it and seek medical help right away. If your condition worsens, or if symptoms last more than five days or come back after improving, consult a healthcare professional.

Overdose

If you or someone else accidentally takes too much of a medication, it’s important to seek medical attention right away. Signs of an overdose can vary, but they may include unusual symptoms or changes in behavior.

Always err on the side of caution—if you suspect an overdose, don’t hesitate to contact a healthcare professional or go to the nearest emergency room. Your health and safety are the top priority.

Pregnancy Use

If you are pregnant or breastfeeding, it is important to avoid using this medication. The potential risks to your baby during pregnancy and while nursing are significant, and it is best to prioritize your health and your child's safety. Always consult with your healthcare provider for guidance on safe treatment options during this time.

Lactation Use

If you are breastfeeding, it is important to avoid using this medication. There are potential risks associated with its use during breastfeeding, and it is not recommended for nursing mothers. Always consult with your healthcare provider for guidance on safe medication options while you are breastfeeding. Your health and the well-being of your baby are paramount, so make sure to discuss any concerns or questions you may have.

Pediatric Use

It's important to keep this product out of reach of children to ensure their safety. If you are pregnant or breastfeeding, you should not use this product. Remember, it is meant for external use only. If your child accidentally ingests it, seek medical attention right away.

Before applying the product more broadly, test it on a small area of skin to check for any sensitivities or reactions. This precaution helps ensure that your child can use it safely.

Geriatric Use

While there is no specific information about how this medication should be used by 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.

Remember, even if there are no specific dosage adjustments or safety concerns mentioned, your healthcare provider may still recommend monitoring for any potential side effects or interactions with other medications you may be taking. Always prioritize open communication with your healthcare team to ensure the best care.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment is safe and effective for your specific condition. They can help determine the best approach for managing your health, especially if you have concerns about your kidneys.

Hepatic Impairment

If you have been diagnosed with liver disease, it is important to avoid using this medication. Liver disease can affect how your body processes medications, and using this drug could lead to serious health risks. Always consult with your healthcare provider for guidance tailored to your specific condition and treatment options. Your safety is the top priority, so make sure to discuss any liver-related concerns with your doctor.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication may not interfere with other drugs or tests. However, every individual is different, and your healthcare provider can help ensure that your treatment plan is safe and effective for you.

Always discuss any changes in your medications or upcoming lab tests with your healthcare provider to avoid any potential issues and to get the best care possible.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dark place or refrigerate it. This helps maintain its effectiveness. Always check the expiration date and discard the product after this date to avoid any potential risks. Proper storage and timely disposal are key to your safety and the product's reliability.

Additional Information

You will apply the medication topically, which means you will apply it directly to your skin. Before using it for treatment, it's important to test a small area of your skin to check for any sensitivities or allergies. If you experience any adverse reactions, such as irritation or other sensitivities, stop using the product immediately and seek medical attention.

Always be cautious and monitor your skin's response to the medication. If you notice any irritation, discontinue use and consult a healthcare professional.

FAQ

What is the primary use of this drug?

This drug temporarily relieves pain, itching, or swelling associated with anorectal disorders.

How should I apply the drug?

Spray the anesthetic spray sparingly on the affected area. You should test it on a small area of skin for sensitivities before full use.

What should I do if I experience irritation?

If you experience any irritation or sensitivity, discontinue use immediately and seek medical attention.

Are there any contraindications for using this drug?

Do not use this drug if you are pregnant, breastfeeding, have a history of seizures, liver disease, or an allergy to any of the ingredients.

What precautions should I take when using this drug?

Avoid using in large quantities, particularly over raw surfaces or blistered areas, and avoid contact with the eyes. If contact occurs, rinse with eyewash and seek medical attention.

What should I do if I accidentally ingest the drug?

If accidentally ingested, seek medical attention immediately.

How should I store this drug?

Store in a cool, dark place or refrigerate, and discard after the expiration date.

What if my symptoms persist?

If your condition worsens or symptoms persist for more than five days, consult with a medical professional immediately.

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 product is identified by the SPL code 34089-3. No additional specific description details are provided.

Uses and Indications

This drug is indicated for the temporary relief of pain, itching, or swelling associated with anorectal disorders.

Limitations of Use This product is for external use only.

Dosage and Administration

Prior to therapeutic use, it is essential for healthcare professionals to conduct a sensitivity test by applying a small amount of UberNumb anesthetic spray to a limited area of the skin. This step is crucial to identify any potential allergies or sensitivities.

UberNumb should be applied sparingly to the affected area. Following application, patients can expect to experience numbing relief within approximately two minutes. For sustained numbing effects, reapplication of UberNumb may be performed as needed, ensuring that it is applied sparingly each time.

In the event that any irritations or sensitivities arise during use, it is imperative to discontinue application immediately and seek appropriate medical attention.

Contraindications

Use is contraindicated in the following situations:

Pregnancy and lactation: The product should not be used by individuals who are pregnant or breastfeeding due to potential risks to the fetus or infant.

Seizure history: Individuals with a history of seizures should not use this product, as it may exacerbate their condition.

Liver disease: The use of this product is contraindicated in patients diagnosed with liver disease due to the potential for adverse effects on liver function.

Allergy to ingredients: Patients with known allergies to any of the listed ingredients should avoid using this product to prevent allergic reactions.

Additionally, the product should not be applied in large quantities, especially over raw surfaces or blistered areas. Contact with the eyes must be avoided; in case of contact, rinse thoroughly with eyewash and seek immediate medical attention. Prior to full application, a small area of skin should be tested for sensitivities. If any reaction or sensitivity occurs, discontinue use and seek medical attention. If the condition worsens or symptoms persist for more than five days, or recur after resolution, consult a medical professional promptly.

Warnings and Precautions

The use of this product is contraindicated in certain populations and situations. It is imperative that healthcare professionals adhere to the following warnings and precautions to ensure patient safety.

Contraindications This product should not be used in individuals who are pregnant or breastfeeding. Additionally, it is contraindicated for patients with a history of seizures, those diagnosed with liver disease, and individuals with known allergies to any of the ingredients listed.

External Use Only This product is intended for external use only. In the event of accidental ingestion, immediate medical attention is required. It is crucial to avoid applying the product in large quantities, particularly on raw surfaces or blistered areas.

Eye Contact Contact with the eyes must be strictly avoided. Should contact occur, the affected area should be rinsed thoroughly with copious amounts of eyewash, and medical attention should be sought immediately.

Sensitivity Testing Prior to widespread application, it is recommended to conduct a patch test on a small area of skin to assess for any sensitivities.

Adverse Reactions If a reaction or sensitivity occurs, the use of the product should be discontinued immediately, and medical attention should be sought. Healthcare professionals should advise patients to consult with a medical professional if their condition worsens, if symptoms persist for more than five days, or if symptoms recur after resolution.

Emergency Medical Help In cases of accidental ingestion or eye contact, immediate medical assistance is essential.

By adhering to these warnings and precautions, healthcare professionals can help mitigate risks associated with the use of this product and ensure patient safety.

Side Effects

Patients should be aware of several important warnings and precautions associated with the use of this product. It is contraindicated for use in individuals who are pregnant or breastfeeding. The product is intended for external use only; if ingested accidentally, patients should seek medical attention immediately. Caution is advised against using the product in large quantities, particularly on raw surfaces or blistered areas. Additionally, contact with the eyes should be strictly avoided; in the event of contact, patients should rinse the eyes thoroughly with copious amounts of eyewash and seek medical attention without delay.

Prior to use, it is recommended that patients apply the product to a small area of skin to test for any sensitivities. The product should not be used by individuals with a history of seizures or those diagnosed with liver disease. Furthermore, patients with known allergies to any of the listed ingredients should refrain from using the product. Should any reaction or sensitivity occur, it is imperative to discontinue use and seek medical attention immediately. If the condition worsens or symptoms persist for more than five days, or if symptoms recur after initially clearing up, patients are advised to consult with a medical professional promptly.

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 (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Uber Numb.
Details

Pediatric Use

Pediatric patients should be monitored closely, as the product is intended for external use only. It is crucial to keep the product out of reach of children to prevent accidental ingestion, which necessitates immediate medical attention. Prior to widespread application, a small area of skin should be tested for sensitivities to ensure safety and tolerability. The product is not recommended for use in pregnant or breastfeeding individuals.

Geriatric Use

There is no specific information 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

Pregnant patients and those who are breastfeeding should not use this medication. The potential risks associated with the use of this drug during pregnancy have not been established, and its safety profile in lactating women is also unclear. Healthcare professionals are advised to consider alternative treatments for women who are pregnant or breastfeeding to avoid any potential adverse effects on fetal outcomes or infant health.

Lactation

Lactating mothers are advised against the use of this medication while breastfeeding. There is insufficient data regarding the excretion of the drug in human breast milk and its effects on breastfed infants. Therefore, the potential risks to the nursing infant outweigh any possible benefits of treatment in lactating individuals.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment should not use this medication if they have been diagnosed with liver disease. Due to the potential for altered pharmacokinetics and increased risk of adverse effects, it is essential to avoid administration in this population. Monitoring of liver function is recommended for patients who may have compromised liver function, and appropriate dosage adjustments or alternative therapies should be considered based on the severity of the impairment.

Overdosage

In the event of an overdosage, it is imperative that medical attention is sought immediately. Healthcare professionals should be aware that prompt intervention is crucial in managing potential complications associated with overdosage.

Symptoms of overdosage may vary depending on the specific substance involved, but they can include a range of adverse effects that necessitate careful monitoring and management.

Management procedures should include a thorough assessment of the patient's condition, including vital signs and any presenting symptoms. Supportive care may be required, and specific treatment protocols should be followed based on the substance involved and the severity of the symptoms.

In all cases of suspected overdosage, it is essential to contact poison control or a specialized medical facility for guidance on the appropriate course of action.

Nonclinical Toxicology

Use of this product is contraindicated in pregnant or breastfeeding individuals due to potential teratogenic effects. In the event of a reaction or sensitivity, it is advised to discontinue use and seek medical attention immediately. Should the condition worsen or if symptoms persist for more than five days, or recur after resolution, consultation with a medical professional is recommended.

No relevant information is available regarding carcinogenicity, mutagenicity, or animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients not to use the product if they are pregnant or breastfeeding. It is important to emphasize that the product is for external use only. Instruct patients that if the product is accidentally ingested, they should seek medical attention immediately.

Providers should caution patients against using the product in large quantities, especially over raw surfaces or blistered areas, to prevent potential adverse effects. Additionally, patients should be informed to avoid contact with the eyes. In the event of eye contact, they should rinse the eyes with copious amounts of eyewash and seek medical attention without delay.

Before applying the product more broadly, healthcare providers should recommend that patients test it on a small area of skin to check for any sensitivities. This precaution can help identify any adverse reactions prior to full application.

Storage and Handling

The product is supplied in a configuration that ensures optimal preservation of its integrity. It is recommended to store the product in a cool, dark place or to refrigerate it to maintain its efficacy.

Healthcare professionals should ensure that the product is discarded after the expiration date to prevent the use of ineffective or potentially harmful materials. Proper adherence to these storage and handling guidelines is essential for maintaining product quality and safety.

Additional Clinical Information

The product is administered topically. Clinicians should advise patients to conduct a patch test on a small area of skin prior to therapeutic use to check for sensitivities and potential allergies. If any adverse reactions occur, patients are instructed to seek medical attention immediately. Additionally, if irritations or other sensitivities develop during use, patients should discontinue application and consult a healthcare professional.

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.