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Electrum Numb Foam

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Active ingredient
Lidocaine Hydrochloride 1.92 g/48 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Soap
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2021
Label revision date
April 25, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 1.92 g/48 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Soap
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 2021
Label revision date
April 25, 2025
Manufacturer
RENU LABORATORIES, LLC
Registration number
M017
NDC root
76348-596
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

Electrum Numb Foam is a foaming anesthetic designed to provide temporary relief from discomfort and pain associated with various skin procedures, such as tattoo removal, dermarolling, electrolysis, microblading, and piercing. In addition to alleviating pain and itch, it helps prevent infection while also serving as a gentle cleaning option for minor cuts, scrapes, and burns.

This product can be used instead of soap and water to clean these minor injuries, making it a versatile addition to your first aid routine. It is suitable for adults and children aged two years and older, offering a supportive solution for managing skin discomfort during and after procedures.

Uses

You can use this product as an alternative to soap and water for cleaning minor cuts, scrapes, and burns. It’s designed to help you maintain cleanliness while promoting healing.

Additionally, it provides temporary relief from discomfort and pain associated with various skin procedures, including tattoo removal, dermarolling, electrolysis, microblading, and piercing. This product not only alleviates pain and itching but also helps prevent infection, making it a useful option for your skincare needs.

Dosage and Administration

Before using the foam soap, make sure to shake the bottle well to mix the ingredients properly. When you're ready, apply 2 to 3 pumps of the foam soap onto your skin and gently rub it in. It's important to let the soap sit on your skin for 5 to 10 minutes to allow it to work effectively.

After the time is up, rinse the soap off gently with running water or wipe it away using a clean paper towel. You should use this foam soap before, during, and after your procedure to ensure the best results.

What to Avoid

It's important to use this medication safely to avoid potential issues. Do not apply it to your eyes or large areas of your body. Additionally, you should not use it for more than one week unless your doctor specifically instructs you to do so. Be cautious about using large amounts, especially on raw surfaces or blistered areas.

Before using this medication, consult your doctor if you have deep or puncture wounds, animal bites, or serious burns. This will help ensure that you use the product appropriately and safely.

Side Effects

You should be aware that this product is for external use only. Avoid getting it in your eyes and do not apply it to large areas of your body or use it for longer than one week unless your doctor advises otherwise. It's important not to use large amounts, especially on raw or blistered skin. If you have deep or puncture wounds, animal bites, or serious burns, consult your doctor before using this product.

If your condition worsens, or if your symptoms last more than seven days or improve and then return within a few days, you should stop using the product and seek medical advice.

Warnings and Precautions

This product is for external use only, so please avoid getting it in your eyes and do not apply it to large areas of your body. It's important not to exceed the recommended dosage unless your doctor advises you to do so. Additionally, you should not use it for more than one week without a doctor's guidance, and be cautious about using it in large amounts, especially on raw or blistered skin.

If you have deep or puncture wounds, animal bites, or serious burns, consult your doctor before using this product. If you accidentally swallow it, seek emergency medical help or contact a Poison Control Center immediately. You should also stop using the product and call your doctor if your condition worsens, if symptoms last longer than seven days, or if they improve and then return within a few days.

Overdose

Taking more medication than recommended can lead to serious health issues. It’s important to follow the dosage instructions provided by your doctor or on the medication label. If you accidentally take too much, you may experience symptoms such as confusion, dizziness, or unusual behavior.

If you suspect an overdose, seek immediate medical help. Call your local emergency number or go to the nearest hospital. Remember, it’s always better to be safe and get checked out if you’re unsure about your symptoms or the amount of medication you’ve taken.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there are no specific guidelines or warnings about using Electrum Numb Foam during this time. The information available does not indicate any risks or contraindications associated with lidocaine, the active ingredient in the foam, for pregnant individuals. Additionally, there are no recommended dosage changes for those who are pregnant, nor are there any special precautions mentioned regarding its use.

As always, it's best to consult with your healthcare provider before using any medication during pregnancy to ensure it is safe for you and your baby.

Lactation Use

If you are breastfeeding, you can use Electrum Numb Foam without specific warnings or recommendations against it. Currently, there is no information available about whether this product is passed into breast milk or if it poses any risks to your baby.

As always, it's a good idea to consult with your healthcare provider if you have any concerns about using new products while nursing. They can provide personalized advice based on your situation.

Pediatric Use

You can use this product for children aged 2 years and older. However, if your child is under 2 years old, it's important to consult with a doctor before using it. This ensures that the product is safe and appropriate for your little one. Always prioritize your child's health by seeking professional advice when needed.

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 best approach for you or your loved one, considering any existing health conditions or medications that may interact.

Remember, your safety and well-being are the top priority, so don’t hesitate to ask questions and discuss any concerns with your doctor.

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 may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver function and how it relates to your treatment. They can help ensure that your medication 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 specific health needs.

Always keep your healthcare team informed about all the medications and supplements you use, as well as any lab tests you may undergo. This way, they can provide the best care tailored to you.

Storage and Handling

To ensure the product remains fresh and effective, always keep the bottle tightly closed. Store it at room temperature, away from extreme heat or cold. It's important to keep this product out of reach of children to prevent accidental ingestion. If the product is swallowed, seek medical assistance or contact a Poison Control Center immediately for guidance.

Additional Information

No further information is available.

FAQ

What is Electrum Numb Foam used for?

Electrum Numb Foam can be used instead of soap and water to help clean minor cuts, scrapes, and burns, and provides temporary relief of discomfort and pain associated with dermal procedures.

How do I use Electrum Numb Foam?

Shake well before each use, apply 2 to 3 pumps of foam soap, gently rub into the skin, leave it on for 5 to 10 minutes, and then rinse off gently with running water or wipe with a clean paper towel.

Who can use Electrum Numb Foam?

Electrum Numb Foam is for adults and children 2 years old and older. Children under two years of age should ask a doctor before use.

Are there any contraindications for using Electrum Numb Foam?

No specific contraindications are mentioned, but do not use in the eyes or on large areas of the body.

What should I do if I experience side effects?

Stop using Electrum Numb Foam and ask a doctor if your condition worsens or symptoms persist for more than 7 days.

Can I use Electrum Numb Foam during pregnancy?

There are no specific statements regarding the use of Electrum Numb Foam during pregnancy, and no contraindications are mentioned.

What precautions should I take when using Electrum Numb Foam?

Avoid contact with eyes, do not exceed the recommended dosage, and do not use for longer than 1 week unless directed by a doctor.

What should I do if Electrum Numb Foam is swallowed?

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

How should I store Electrum Numb Foam?

Store at room temperature, keep the bottle tightened to maintain freshness, and keep it out of reach of children.

Packaging Info

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

Packaging configurations for Electrum Numb Foam.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No specific information related to the Description section for SPL code 34089-3 is provided in the text.

Uses and Indications

This drug is indicated for the cleansing of minor cuts, scrapes, and burns as an alternative to soap and water. It is also indicated for the temporary relief of discomfort and pain associated with various dermal procedures, including tattoo removal, tattoo application, dermarolling, electrolysis, microblading, and piercing.

Additionally, this drug provides temporary relief from pain and itching while assisting in the prevention of infection.

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

Dosage and Administration

Healthcare professionals are advised to shake the product well before each use. For application, 2 to 3 pumps of foam soap should be dispensed and gently rubbed into the skin. The product should be left on the skin for a duration of 5 to 10 minutes to ensure optimal efficacy. Following this period, the product must be rinsed off gently with running water or wiped away using a clean paper towel.

This product is indicated for use before, during, and after the procedure to maintain appropriate hygiene and skin preparation.

Contraindications

Use is contraindicated in the eyes and on large areas of the body. Prolonged use beyond one week is not recommended unless directed by a healthcare professional. Application in large quantities, particularly over raw surfaces or blistered areas, is also contraindicated. Additionally, consultation with a healthcare provider is advised prior to use in patients with deep or puncture wounds, animal bites, or serious burns.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes. The recommended dosage should not be exceeded unless specifically directed by a healthcare professional.

General precautions must be observed to ensure safe use. This product should not be applied to the eyes or used on large areas of the body. Prolonged use beyond one week is not advised unless directed by a physician. Caution is advised against using large quantities, particularly over raw surfaces or blistered areas. Patients should consult a healthcare provider prior to use if they have deep or puncture wounds, animal bites, or serious burns.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Users should discontinue use and consult a healthcare professional if the condition worsens, if symptoms persist for more than seven days, or if symptoms resolve and then recur within a few days.

Side Effects

Patients using this product may experience a range of adverse reactions. It is important to note that the product is intended for external use only, and contact with the eyes should be strictly avoided. Patients are advised not to exceed the recommended dosage unless directed by a healthcare professional.

In clinical practice, the product should not be used in the eyes or applied to large areas of the body. Additionally, it should not be used for longer than one week unless specifically directed by a doctor. Caution is advised when applying the product in large quantities, particularly over raw surfaces or blistered areas.

Patients should discontinue use and consult a healthcare provider if their condition worsens, if symptoms persist for more than seven days, or if symptoms clear up and then recur within a few days. Furthermore, individuals should seek medical advice before using the product if they have deep or puncture wounds, animal bites, or serious burns.

Drug Interactions

There are no specific drug interactions associated with the use of this medication. Additionally, no laboratory test interactions have been identified in the available data. 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 Electrum Numb Foam (lidocaine hci). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Electrum Numb Foam.
Details

Pediatric Use

Pediatric patients aged 2 years and older may use the product. For children under 2 years of age, it is advised to consult a healthcare professional prior to use.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

There are no specific statements regarding the use of Electrum Numb Foam during pregnancy. The prescribing information does not mention any contraindications or risks associated with the use of lidocaine during pregnancy. Additionally, no dosage modifications for pregnant individuals are provided. The insert does not include any special precautions regarding the use of this product during pregnancy. As such, healthcare professionals should consider the absence of data when advising pregnant patients or women of childbearing potential regarding the use of this product.

Lactation

There are no specific warnings or recommendations regarding the use of Electrum Numb Foam in lactating mothers. Additionally, there is no information available about the potential for excretion of the product in breast milk or any associated risks to breastfed infants.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the lack of information necessitates careful clinical judgment and monitoring of these patients.

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

Overdosage of the medication can lead to serious health consequences. It is imperative that healthcare professionals adhere to the recommended dosage guidelines and avoid exceeding these limits unless specifically directed by a physician.

In the event of suspected overdosage, it is crucial to monitor the patient for any potential symptoms that may arise. Symptoms of overdosage can vary depending on the specific medication involved and may include a range of physiological and psychological effects.

Management of overdosage should be initiated promptly. Healthcare providers are advised to assess the patient's condition thoroughly and implement appropriate interventions. This may include supportive care, symptomatic treatment, and, if necessary, the use of specific antidotes or other medical interventions as dictated by the clinical scenario.

In all cases of overdosage, it is recommended to contact a poison control center or seek immediate medical assistance to ensure the patient receives the necessary care and monitoring.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

Postmarketing experience has identified the following adverse reactions reported voluntarily or through surveillance programs: allergic reactions, including anaphylaxis, as well as skin reactions such as rash, pruritus, and erythema.

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 a Poison Control Center immediately. This precaution is crucial to ensure the safety and well-being of children who may inadvertently access the medication.

Storage and Handling

The product is supplied in a bottle that should be kept tightly closed to maintain its freshness and effectiveness. It is recommended to store the product at room temperature. Additionally, it is important to keep the product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Electrum Numb Foam, 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 Electrum Numb Foam, 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

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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.