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Walgreens Burn Relief

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This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2018
Label revision date
May 9, 2019
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Dosage form
Gel
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 2018
Label revision date
May 9, 2019
Manufacturer
Walgreens
Registration number
part348
NDC root
0363-0290
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

Burn Gel LIDOCAINE HCl 4% is a topical analgesic designed to provide temporary relief from pain and itching caused by minor burns, sunburn, cuts, scrapes, insect bites, and other minor skin irritations. This gel contains Vitamin E and Aloe, which can help soothe the skin, and is marketed as a maximum strength option for effective relief.

When applied, Burn Gel works quickly to alleviate discomfort associated with these skin conditions, making it a helpful choice for managing minor injuries. Whether you're dealing with a sunburn or a small cut, this product aims to ease your pain and promote comfort.

Uses

You can use this medication to temporarily relieve pain and itching caused by various skin issues. It is effective for minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations. This means that if you experience discomfort from any of these conditions, this product can help soothe your skin and provide some relief.

Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

When using this medication, you should apply it to the affected area no more than 3 to 4 times a day if you are an adult or a child aged 2 years and older. This helps ensure that you get the best results while minimizing any potential side effects.

If your child is under 2 years old, it’s important to consult with a doctor before using this medication. They can provide guidance on the appropriate treatment for younger children. Always follow these instructions carefully to ensure safe and effective use.

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 can 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

This product is intended for external use only, so be sure to avoid applying it in large amounts, especially on raw or blistered skin. While using it, take care 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, stop using the product and consult your doctor. Additionally, keep this product out of reach of children, and 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, so please avoid applying it to large areas of your skin, especially over raw or blistered surfaces. Be careful not to get it in your eyes.

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 consult your doctor. Additionally, keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately.

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. Acting quickly can make a significant difference in the outcome.

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, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

When it comes to using this medication during pregnancy, there are no specific guidelines or safety concerns outlined in the information provided. This means that the effects of the medication on pregnant individuals and their developing babies are not clearly defined.

If you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before starting any new medication. They can help you understand any potential risks and make informed decisions about your health and the health of your baby. Always prioritize open communication with your healthcare team regarding any medications you may be considering.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the use of this medication during nursing. This means that the effects on breast milk and your nursing infant are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding. They can help you weigh the benefits and risks to ensure the safety of both you and your baby.

Pediatric Use

When using this medication for children aged 2 years and older, you can apply it to the affected area no more than 3 to 4 times a day. However, if your child is under 2 years old, it’s important to consult a doctor before use.

Always keep this medication out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately. Your child's safety is a priority, so following these guidelines is essential.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it’s important to discuss any potential risks and benefits with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances. Always prioritize open communication about any concerns you may have regarding medication use.

Renal Impairment

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

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help you understand how to manage your treatment effectively while considering your kidney health.

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 if you have hepatic impairment (issues with liver function).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

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 share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

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 sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

If you accidentally swallow this medication, it's important to seek medical help immediately or contact a Poison Control Center. This ensures you receive the appropriate care and guidance. There are no additional details available regarding laboratory tests, abuse potential, or how to take the medication.

FAQ

What is Burn Gel LIDOCAINE HCl 4% used for?

Burn Gel LIDOCAINE HCl 4% temporarily relieves pain and itching due to minor burns, sunburn, minor cuts, scrapes, insect bites, and minor skin irritations.

How should I apply Burn Gel LIDOCAINE HCl 4%?

Adults and children 2 years and over should apply it 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?

No specific contraindications are mentioned for Burn Gel LIDOCAINE HCl 4%.

What should I avoid while using this product?

Do not use in large quantities, especially over raw surfaces or blistered areas, and avoid getting it into your eyes.

What should I do if my condition worsens?

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

How should I store Burn Gel LIDOCAINE HCl 4%?

Store the gel between 20 °C and 25 °C (68 °F and 77 °F).

What should I do if the gel is swallowed?

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

Is there any information about using this gel during pregnancy or while nursing?

The provided information does not specify any details regarding use during pregnancy or nursing.

Packaging Info

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

Packaging configurations for Walgreens Burn Relief.
Details

Drug Information (PDF)

This file contains official product information for Walgreens Burn Relief, 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 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.

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. It is important to ensure that the application is performed gently and that the area is clean prior to use.

For children under 2 years of age, it is advised to consult a physician before use to determine the appropriate course of action.

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

For external use only. It is imperative that the product is not applied in large quantities, especially on raw surfaces or blistered areas, to prevent potential adverse effects. Care should be taken to avoid contact with the eyes, as this may lead to irritation or injury.

Healthcare professionals should advise patients to discontinue use and seek medical advice if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. These actions are crucial to ensure patient safety and to facilitate appropriate medical intervention if necessary.

Additionally, it is essential to keep this product 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 to ensure prompt and effective management of the situation.

Side Effects

Patients should be aware that this product is for external use only. It is advised not to use the product in large quantities, particularly over raw surfaces or blistered areas, as this may lead to adverse effects.

During use, patients should take care to avoid 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 instructed to stop use and consult a healthcare professional.

Additionally, this product should be kept out of reach of children. In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 Walgreens Burn Relief (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Walgreens Burn Relief.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area no more than 3 to 4 times daily. For children under 2 years of age, it is advised to consult a physician before use.

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 with a Poison Control Center is recommended.

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, given the lack of targeted data.

Pregnancy

Pregnant patients should be aware that the safety of this medication during pregnancy has not been specifically established. There are no available data regarding the potential risks or fetal impacts associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to weigh the potential benefits against any unknown risks. It is recommended that pregnant patients discuss their treatment options with their healthcare provider to ensure informed decision-making regarding the use of this medication during pregnancy.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or any lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established, and further data may be necessary to inform clinical decisions.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the drug insert text regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as there is no available data to guide dosing or monitoring in this population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this medication. Consequently, there are no 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 prescribing 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 should include supportive care and symptomatic treatment as necessary. Continuous evaluation of the patient's condition is recommended to address any complications that may arise.

Nonclinical Toxicology

There is currently no available data regarding teratogenic or non-teratogenic effects associated with the substance. Additionally, no relevant information has been identified in the context of nonclinical toxicology, including animal pharmacology and toxicology. As such, the assessment of these parameters remains unaddressed in the existing studies.

Postmarketing Experience

No postmarketing experience details are available in the insert.

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, to avoid potential complications.

Patients should be instructed to discontinue use and consult a doctor 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 and seek medical advice.

Providers should emphasize the importance of avoiding contact with the eyes, as this could lead to irritation or other adverse effects.

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 maintain its efficacy and stability. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable container that protects it from environmental factors. Special handling requirements should be followed to prevent any compromise to the product's integrity.

Additional Clinical Information

Patients should be advised that if the medication is swallowed, they must seek medical help or contact a Poison Control Center immediately. No further information is available regarding laboratory tests, abuse potential, route, method, or frequency of administration, nor is there any additional data from postmarketing experience.

Drug Information (PDF)

This file contains official product information for Walgreens Burn Relief, 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 Walgreens Burn Relief, 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.