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Cvs Maximum Strength Burn

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Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2022
Label revision date
December 3, 2025
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2022
Label revision date
December 3, 2025
Manufacturer
CVS Pharmacy
Registration number
M017
NDC root
69842-309

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Drug Overview

Maximum Strength Burn Gel is a topical analgesic that contains 4% lidocaine HCl, which helps to temporarily relieve pain and itching. You can use it for various skin irritations, including minor burns, sunburn, minor cuts, scrapes, and insect bites.

In addition to its pain-relieving properties, this gel is formulated with soothing aloe and vitamin E, which can help to calm and nourish your skin. Whether you're dealing with a sunburn or a minor cut, this product is designed to provide quick relief and comfort.

Uses

You can use this product to temporarily relieve pain and itching caused by various skin issues. It’s effective for minor burns, sunburn, minor cuts, scrapes, insect bites, and other minor skin irritations. Whether you’re dealing with discomfort from a sunburn or a pesky insect bite, this product can help soothe your skin and provide relief.

Feel confident using it for past pain and itch relief as well. It’s designed to help you feel more comfortable and get back to your daily activities without the distraction of skin irritation.

Dosage and Administration

If you or your child is 2 years old or older, you can apply the medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results. However, if your child is under 2 years old, it’s important to consult a doctor before using the medication. This will help ensure safety and effectiveness for younger children.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should not apply it in large quantities, especially on raw or blistered areas of your skin, as this could lead to irritation or other complications. Additionally, be careful to avoid getting the medication in your eyes, as this can cause discomfort or damage.

While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this medication, following these guidelines will help ensure your safety and the effectiveness of your treatment. Always consult with your healthcare provider if you have any questions or concerns.

Side Effects

When using this product, it's important to remember that it is for external use only. Avoid applying it in large amounts, especially on raw or blistered skin, and be careful not to get it in your eyes. If your condition worsens, if symptoms persist for more than seven days, or if symptoms improve and then return within a few days, you should stop using the product.

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

Warnings and Precautions

This product is intended for external use only. Be cautious when applying it, especially on large areas of skin, raw surfaces, or blistered areas. Avoid contact with your eyes, as this can cause irritation.

If your condition worsens, if symptoms persist for more than 7 days, or if symptoms improve and then return within a few days, stop using the product and call your doctor. In case of accidental ingestion, seek medical help immediately or contact a Poison Control Center.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, acting quickly can make a significant difference in the outcome.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of using this product during pregnancy has not been established. It is generally not recommended for use while pregnant due to potential risks to your developing baby. There may be specific risks to the fetus associated with the use of lidocaine, so it’s crucial to consult your healthcare provider before using this product. They can provide guidance on whether it’s appropriate for you and may suggest dosage adjustments if necessary. Always seek medical advice to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Currently, there is no information available about whether this product is excreted in breast milk or if it poses any risk to your infant.

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

Pediatric Use

If your child is under 2 years old, it's important to consult a doctor before using this medication. For children aged 2 years and older, you can apply the medication to the affected area, but be sure to do this no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

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. 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 the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

It's always best to discuss your liver condition 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 or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20 °C and 25 °C (68 °F and 77 °F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a clean environment to avoid contamination. Always follow any specific instructions provided with the product for safe use and disposal. Keeping these guidelines in mind will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is Maximum Strength Burn Gel used for?

Maximum Strength Burn Gel temporarily relieves pain and itching due to minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.

How should I use Maximum Strength Burn Gel?

For adults and children 2 years and over, apply to the affected area not more than 3 to 4 times daily. For children under 2 years, consult a doctor.

Are there any contraindications for using this gel?

There are no specific contraindications mentioned, but it is not recommended for use in large quantities, particularly over raw surfaces or blistered areas.

Can I use Maximum Strength Burn Gel during pregnancy?

Safety during pregnancy has not been established, and there may be risks to the fetus. Pregnant women should seek medical advice before using this product.

What should I do if I accidentally swallow the gel?

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

What are the storage conditions for this gel?

Store Maximum Strength Burn Gel between 20 °C and 25 °C (68 °F and 77 °F).

What should I do if my condition worsens or does not improve?

Stop use and call your doctor if your condition gets worse, symptoms last for more than 7 days, or symptoms clear up and occur again within a few days.

Is there any information about using this gel while nursing?

There are no specific warnings or recommendations regarding the use of this product in nursing mothers.

Packaging Info

Below are the non-prescription pack sizes of Cvs Maximum Strength Burn (lidocaine hydrochloride 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Maximum Strength Burn.
Details

Drug Information (PDF)

This file contains official product information for Cvs Maximum Strength Burn, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations. It is specifically formulated for use on sunburns and minor burns, providing effective relief from discomfort.

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

Dosage and Administration

For adults and children aged 2 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. The application should be performed with clean hands, ensuring that the area is dry before applying the product.

For children under 2 years of age, it is advised to consult a physician prior to use.

Contraindications

Use is contraindicated in the following situations:

Application in large quantities, especially over raw surfaces or blistered areas, is not recommended due to the potential for adverse effects. Additionally, contact with the eyes should be strictly avoided to prevent irritation or injury.

Warnings and Precautions

The product is intended for external use only. It is imperative to avoid application in large quantities, especially on raw surfaces or blistered areas, as this may lead to adverse effects.

Care should be taken to prevent contact with the eyes. In the event of accidental exposure, immediate rinsing with water is recommended.

Healthcare professionals should advise patients to discontinue use and seek medical attention if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or symptoms resolve and then recur within a few days.

In cases of ingestion, it is crucial to obtain medical assistance or contact a Poison Control Center without delay to ensure appropriate management.

Side Effects

Patients should be aware that the product is for external use only. It is important to avoid applying the product in large quantities, particularly over raw surfaces or blistered areas, as this may lead to adverse reactions.

While using the product, care should be taken to prevent contact with the eyes. If the condition being treated worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days, patients are advised to discontinue use and consult a healthcare professional.

Additionally, the product should be kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Cvs Maximum Strength Burn (lidocaine hydrochloride 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Maximum Strength Burn.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a healthcare professional before use. For children aged 2 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

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 potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Safety during pregnancy has not been established for this product. Use is not recommended during pregnancy due to potential risks to the fetus associated with the use of lidocaine. Pregnant patients should seek medical advice before using this product, and healthcare providers should be consulted for any necessary dosage adjustments if a patient is pregnant. It is important to consider the potential risks to fetal outcomes when making treatment decisions for pregnant women or women of childbearing potential.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion 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 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 event of an overdosage, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous evaluation and appropriate interventions should be implemented based on the clinical presentation and severity of symptoms.

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 seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important to inform patients that the product should not be applied in large quantities, especially over raw surfaces or blistered areas, as this may exacerbate their condition.

Patients should be instructed to discontinue use if their condition worsens or if symptoms persist for more than 7 days. Additionally, they should be made aware that if symptoms resolve and then reoccur within a few days, they should also stop using the product.

Healthcare providers must emphasize the importance of avoiding contact with the eyes, as this could lead to irritation or other complications.

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 within the temperature range of 20 °C to 25 °C (68 °F to 77 °F) to ensure its stability and efficacy. Proper storage conditions must be maintained, and the product should be kept in its original container to protect it from environmental factors. Special handling requirements should be observed to prevent exposure to extreme temperatures or conditions that may compromise the product's integrity.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Cvs Maximum Strength Burn, 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 Cvs Maximum Strength Burn, 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.

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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.