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Walg Aftrsn Burn Relief

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 0.5 mg/100 mg
Other brand names
Dosage form
Spray
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
October 5, 2017
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 0.5 mg/100 mg
Other brand names
Dosage form
Spray
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
October 5, 2017
Manufacturer
Walgreen Company
Registration number
part348
NDC root
0363-9919
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

Lidocaine 0.5% is a topical medication designed to provide temporary relief from pain and itching. It is commonly used for soothing discomfort caused by sunburn, minor burns, skin irritations, scrapes, and insect bites. This external analgesic comes in a convenient continuous spray format, making it easy to apply directly to the affected area for effective pain relief.

Uses

You can use this medication for the temporary relief of pain and itching. It is particularly helpful in soothing discomfort caused by sunburn, minor burns, skin irritations, scrapes, and insect bites. If you’re dealing with any of these issues, this product may provide the relief you need.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for many users.

Dosage and Administration

If you are an adult or a child aged 2 years or older, you can apply this 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 not to use this medication without first consulting a doctor. Always prioritize safety and seek professional advice when it comes to younger children.

What to Avoid

It's important to use this product safely. You should avoid using it in large quantities, especially on raw surfaces or areas with blisters, as this could lead to irritation or other issues. Additionally, make sure to keep it away from your eyes to prevent discomfort or injury.

While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this product, following these guidelines will help ensure your experience is safe and effective.

Side Effects

This product is intended for external use only, so it's important to avoid using it in large amounts, especially on raw surfaces or areas with blisters. While using the product, be careful to keep it away from your eyes.

If you notice any unusual reactions or if the product is swallowed, seek medical help immediately or contact a Poison Control Center. Always keep this product out of reach of children to ensure their safety.

Warnings and Precautions

This product is for external use only, so please avoid using it on large areas of your skin, especially over raw surfaces or blisters. It's important to keep the product away from your eyes to prevent irritation.

If you accidentally swallow the product, seek medical help immediately or contact a Poison Control Center. Additionally, make sure to keep this product out of reach of children to ensure their safety. If you experience any unusual reactions while using the product, stop using it and consult your doctor.

Overdose

If you or someone else has swallowed too much of this 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 symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to reach out for help. Remember, acting quickly can make a significant difference in ensuring safety and health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's reassuring to know that there are no specific warnings, precautions, or contraindications related to the use of WALG AFTRSN BURN RELIEF (lidocaine hydrochloride spray) during pregnancy. This means that, based on the information available, it is considered safe for use in this context. However, it's always a good idea to consult with your healthcare provider before using any medication while pregnant to ensure it aligns with your individual health needs.

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. Additionally, there are no known concerns about the product being passed into breast milk or any associated risks for your infant. Always consult with your healthcare provider if you have any questions or concerns about medications while breastfeeding.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 2 years and older, you can apply it to the affected area up to 3-4 times a day. However, if your child is under 2 years old, you should not use this medication without consulting a doctor first.

Always keep the medication out of reach of children. If your child accidentally swallows it, seek medical help or contact a Poison Control Center immediately. Your child's safety is the top priority, so be sure to follow these recommendations closely.

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. If you or a loved one is an older adult, it’s always wise to discuss any medications with a healthcare provider, especially considering factors like kidney function and changes in cognition (thinking and memory) that can occur with age.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for determining the appropriate use of this medication based on individual health needs. Always ensure that any treatment plan is tailored to your specific situation.

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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 (liver issues).

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 you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use with other drugs and 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 new medications or tests with your healthcare provider to avoid potential issues and to get the best care tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Once you open the product, be sure to discard it after use to maintain safety and quality.

By following these simple storage and handling guidelines, you can help ensure that the product remains safe and effective for your needs.

Additional Information

You should apply the medication to the affected area no more than 3 to 4 times a day if you are an adult or a child aged 2 years or older. If your child is under 2 years old, do not use this medication without consulting a doctor first. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is LIDOCAINE 0.5% used for?

LIDOCAINE 0.5% is used for the temporary relief of pain and itching, helping to soothe pain from sunburn, minor burns, skin irritations, scrapes, and insect bites.

How should I use LIDOCAINE 0.5%?

Adults and children 2 years or older should apply it to the affected area not more than 3-4 times daily. Children under 2 years of age should not use it without consulting a doctor.

Are there any warnings for using LIDOCAINE 0.5%?

Yes, it is for external use only. Avoid contact with eyes and do not use in large quantities, especially over raw surfaces or areas with blisters.

What should I do if LIDOCAINE 0.5% is swallowed?

If swallowed, seek medical help or contact a Poison Control Center immediately.

Can I use LIDOCAINE 0.5% during pregnancy or while nursing?

There are no specific warnings or recommendations regarding the use of this product during pregnancy or lactation.

How should I store LIDOCAINE 0.5%?

Store at room temperature, protect from light, and do not freeze. Discard after opening.

Packaging Info

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

Packaging configurations for Walg Aftrsn Burn Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Walgreens Sunburn Relief is a continuous spray formulation containing lidocaine at a concentration of 0.5%, serving as an external analgesic for pain relief. The product is packaged in an 8 oz (227 g) container, designed for ease of application to affected areas.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with various dermatological conditions. It is effective in alleviating and soothing discomfort resulting from sunburn, minor burns, skin irritations, scrapes, and insect bites.

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

Dosage and Administration

For adults and children aged 2 years or 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 with clean hands and that the affected area is properly prepared prior to administration.

For children under 2 years of age, the product should not be used unless directed by a physician. Healthcare professionals are advised to consult with a doctor for appropriate alternatives or recommendations in such cases.

Contraindications

Use is contraindicated in patients with open wounds or blisters, as application in large quantities to these areas may exacerbate the condition. Additionally, contact with the eyes should be strictly avoided to prevent irritation or injury.

Warnings and Precautions

For external use only. This product should not be applied in large quantities, especially on raw surfaces or areas with blisters, as this may lead to adverse effects.

When using this product, it is imperative to avoid contact with the eyes to prevent irritation or injury.

In the event of accidental ingestion, it is crucial to keep this product out of reach of children. If swallowed, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Healthcare professionals are advised to monitor patients for any unusual reactions or complications associated with the use of this product, although no specific conditions for discontinuation have been provided.

Side Effects

Patients should be aware that this product is for external use only. It is important to avoid using it in large quantities, particularly over raw surfaces or areas with blisters, as this may lead to adverse effects. While using this product, patients should take care to avoid contact with the eyes.

In the event of accidental ingestion, it is crucial to keep the product out of reach of children. If swallowed, patients should seek medical help or contact a Poison Control Center immediately.

There are no specific side effects listed in this section; however, patients are advised to stop use and consult a doctor if they experience any unexpected reactions.

Drug Interactions

There are no specific drug interactions identified for the product, nor are there any noted interactions with laboratory tests. As such, no dosage adjustments or monitoring recommendations are necessary based on the available data.

Packaging & NDC

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

Packaging configurations for Walg Aftrsn Burn Relief.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area no more than 3-4 times daily. For children under 2 years of age, the use of this medication is not recommended; consultation with a healthcare professional is advised.

It is important to keep the medication 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

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

Pregnant patients may use WALG AFTRSN BURN RELIEF (lidocaine hydrochloride spray) as there are no specific warnings, precautions, or contraindications regarding its use during pregnancy mentioned in the prescribing information. However, healthcare professionals should consider the potential risks and benefits when recommending this product to pregnant patients. It is advisable to use this medication only if clearly needed and to discuss any concerns with a healthcare provider. As with any medication, the effects on fetal outcomes are not fully established, and caution is warranted.

Lactation

There are no specific warnings or recommendations regarding the use of this product by lactating mothers. Additionally, there are no statements concerning the potential for excretion in breast milk or any associated risks to breastfed infants during the use of this product.

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 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 timely action can significantly impact the outcome of an overdosage situation. Symptoms may vary depending on the specific substance involved, and monitoring for any adverse effects is essential.

Management of overdosage should include supportive care and symptomatic treatment as necessary. It is recommended that healthcare providers follow established protocols for the assessment and management of overdose cases, ensuring that appropriate measures are taken to mitigate potential risks to the patient.

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 product out of reach of children to prevent accidental ingestion. In the event that the product is swallowed, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be cautioned against using this product in large quantities, especially on raw surfaces or areas with blisters, as this may lead to adverse effects. Additionally, healthcare providers should instruct patients to avoid contact with the eyes while using this product.

Patients are encouraged to stop use and consult a doctor if they experience any concerning symptoms or reactions.

Storage and Handling

The product is supplied in configurations that include specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Once opened, the product must be discarded to ensure safety and efficacy.

Additional Clinical Information

Patients aged 2 years and older are advised to apply the medication to the affected area no more than 3 to 4 times daily. For children under 2 years of age, the use of this medication is not recommended without consulting a doctor. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Walg Aftrsn 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 Walg Aftrsn 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

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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.