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Lidocaine Tattoo Wipe

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Active ingredient
Lidocaine Hydrochloride 3 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cloth
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
May 23, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 3 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cloth
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 2025
Label revision date
May 23, 2025
Manufacturer
MD Tattoo Company
Registration number
M017
NDC root
85055-397
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

NUMB is a fast-acting pain-relieving wipe infused with lidocaine (a medication that numbs the skin). It is designed to provide temporary relief from pain and itching associated with minor cuts, burns, sunburns, insect bites, scrapes, and other minor skin irritations.

Each package contains one extra-large wipe, measuring 8 by 7 inches, making it easy to apply to the affected area. This convenient format allows you to quickly address discomfort and promote relief when you need it most.

Uses

You can use this medication for temporary relief from pain and itching caused by various minor skin issues. This includes discomfort from minor cuts, burns, sunburns, insect bites, scrapes, and other minor skin irritations.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

To use this medication effectively, you should apply the wipe thoroughly to the affected area. This is suitable for both adults and children who are two years old and older. You can use the wipe up to 3 to 4 times a day, depending on your needs.

For optimal results, it's important to let the area stay wet for about 1 to 2 minutes after application. This helps ensure that the medication works effectively on the affected skin. Remember to follow these steps for the best outcome!

What to Avoid

It's important to keep this medication out of reach of children. If a child accidentally swallows it, seek medical help or contact the Poison Control Center immediately. There are no specific contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this medication. Always use it responsibly and as directed.

Side Effects

When using this product, it's important to remember that it is for external use only. If you have deep puncture wounds, animal bites, or serious burns, please consult a doctor before use. Avoid applying the product near your eyes; if contact occurs, rinse your eyes thoroughly with water. Additionally, do not use it over large areas of your body or in large amounts.

If your condition worsens or if you develop irritation or a rash that lasts more than 72 hours, stop using the product and seek medical advice.

Warnings and Precautions

This product is for external use only, so please avoid using it on deep puncture wounds, animal bites, or serious burns unless you consult your doctor first. When applying the product, be careful not to get it in your eyes; if that happens, rinse your eyes thoroughly with water. Additionally, do not apply it over large areas of your body or in large amounts.

If your condition worsens or if you develop irritation or a rash that lasts more than 72 hours, stop using the product and contact your doctor. In case of accidental swallowing, seek emergency medical help or contact the Poison Control Center immediately.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's always better to be safe and get checked by a healthcare professional if you have any concerns about your health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be cautious with any medications, including LIDOCAINE TATTOO WIPE. Currently, there is no specific information available about the safety of this product during pregnancy, including any potential risks or necessary dosage adjustments.

Given the lack of guidance, it is advisable to consult with your healthcare provider before using this product. They can help you understand any potential concerns and make informed decisions about your care during pregnancy.

Lactation Use

If you are breastfeeding, it's important to consult your doctor before using this product. There is a possibility that it can be passed into your breast milk, which means your baby could be exposed to it. Because of this potential risk, you should exercise caution when considering its use while nursing. Always prioritize your health and your baby's safety by discussing any concerns with your healthcare provider.

Pediatric Use

When using this product for children aged two years and older, you should apply the wipe thoroughly to the affected area. It can be used up to 3-4 times a day. For the best results, try to keep the area wet for 1-2 minutes after application.

Always keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact the Poison Control Center immediately.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney 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 usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

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 or tests you may be taking. In this case, there are no known interactions with other drugs or laboratory tests. However, always ensure that your healthcare team is aware of all the medications you are using, as this helps them provide the safest and most effective care tailored to your needs.

Remember, even if no interactions are currently noted, your health can change, and new information may arise. Regular discussions with your provider can help you stay informed and safe.

Storage and Handling

To ensure the best performance and safety of your product, store it at room temperature and avoid freezing it. It's important to keep the product in its original packaging until you are ready to use it. Once opened, please remember to discard it to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply the topical treatment thoroughly to the affected area for both adults and children aged two years and older. It can be used up to 3-4 times a day. For optimal results, try to keep the area wet for 1-2 minutes after application. There are no additional details regarding laboratory tests, abuse potential, or patient counseling information.

FAQ

What is NUMB?

NUMB is a fast-acting pain-relieving wipe infused with lidocaine.

What conditions does NUMB help relieve?

NUMB provides temporary relief of pain and itching associated with minor cuts, burns, sunburns, insect bites, scrapes, and minor skin irritations.

How should I use NUMB?

For adults and children two years and older, apply the wipe thoroughly to the affected area up to 3-4 times daily. For best results, allow the area to remain wet for 1-2 minutes.

Are there any warnings for using NUMB?

Yes, NUMB is for external use only. Avoid contact with eyes, and do not apply over large areas of the body or in large quantities. Stop use and consult a doctor if the condition worsens or if irritation lasts more than 72 hours.

What should I do if NUMB is swallowed?

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

Is NUMB safe to use during pregnancy?

There is no specific information regarding the use of NUMB during pregnancy, so consult a doctor before use.

Can nursing mothers use NUMB?

Nursing mothers should consult a doctor before using NUMB due to the potential for excretion in breast milk.

How should I store NUMB?

Store NUMB at room temperature, do not freeze, and keep it in its original packaging until use. Discard after opening.

Are there any contraindications for using NUMB?

No contraindications are listed for NUMB in the provided information.

Packaging Info

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

Packaging configurations for Lidocaine Tattoo Wipe.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

NUMB is a fast-acting, pain-relieving wipe infused with lidocaine. Each package contains one extra-large wipe, measuring 8 x 7 inches. It is designed for topical application to provide localized relief. The product should not be flushed.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor cuts, burns, sunburns, insect bites, scrapes, and minor skin irritations.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

For adults and children aged two years and older, the wipe should be applied thoroughly to the affected area. The application may be performed up to 3-4 times daily. For optimal results, it is recommended that the treated area remains wet for a duration of 1-2 minutes following application.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical assistance should be sought or the Poison Control Center contacted.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to consult a physician if they have deep puncture wounds, animal bites, or serious burns prior to using this product.

When utilizing this product, it is imperative to avoid contact with the eyes. In the event of accidental eye contact, patients should rinse their eyes thoroughly with water. Additionally, the product should not be applied over large areas of the body or in excessive quantities to prevent adverse effects.

Patients must be instructed to discontinue use and seek medical advice if their condition worsens or if irritation or rash develops and persists for more than 72 hours.

In cases of ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Side Effects

Patients using this product should be aware that it is for external use only. It is advised to consult a doctor if there are deep puncture wounds, animal bites, or serious burns prior to use. While using this product, patients should avoid contact with the eyes; in the event of contact, it is important to rinse the eyes thoroughly with water. Additionally, the product should not be applied over large areas of the body or in large quantities.

Patients are instructed to discontinue use and seek medical advice if their condition worsens or if irritation or rash appears and persists for more than 72 hours. These precautions are essential to ensure the safe and effective use of the product.

Drug Interactions

No drug interactions have been identified for the product, indicating that it does not have clinically significant interactions with other medications. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Lidocaine Tattoo Wipe.
Details

Pediatric Use

Pediatric patients aged two years and older may use the product by applying the wipe thoroughly to the affected area. The recommended application frequency is up to 3-4 times daily. For optimal results, it is advised to allow the area to remain wet for 1-2 minutes after application.

Caution is advised as the product should be kept out of reach of children. In the event of accidental ingestion, medical assistance should be sought immediately, or the Poison Control Center should be contacted.

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

There is no specific information regarding the use of LIDOCAINE TATTOO WIPE in pregnant patients, including safety concerns, dosage modifications, or special precautions during pregnancy. Healthcare professionals should consider the lack of data when prescribing this product to women of childbearing potential and weigh the potential risks and benefits. Given the absence of established safety information, caution is advised when administering this product to pregnant patients.

Lactation

Nursing mothers should consult a doctor before using this product. There is a potential for excretion in breast milk, and caution is advised when using this product while breastfeeding due to the risk of infant exposure.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there are no established dosage adjustments, special monitoring requirements, or precautions outlined 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 prudent in these cases, although specific parameters are not defined in the available information.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks 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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact the Poison Control Center immediately. This precaution is vital to ensure the safety and well-being of children who may inadvertently access the medication.

Storage and Handling

The product is supplied in its original packaging, which should be retained until use to ensure optimal integrity. It is essential to store the product at room temperature, avoiding exposure to freezing conditions. Once opened, the product must be discarded to maintain safety and efficacy.

Additional Clinical Information

The product is administered topically, with instructions for adults and children aged two years and older to apply the wipe thoroughly to the affected area. It is recommended to use the product up to 3-4 times daily, allowing the area to remain wet for 1-2 minutes for optimal results.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Lidocaine Tattoo Wipe, 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 Lidocaine Tattoo Wipe, 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.