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Publix Burn Relief

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This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 0.5 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 2012
Label revision date
November 15, 2012
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 0.5 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 2012
Label revision date
November 15, 2012
Manufacturer
Publix Super Markets Inc
Registration number
part348
NDC root
56062-701
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

Publix burn relief Aloe Vera Gel is a soothing gel designed to cool and relieve pain associated with sunburn and other minor skin irritations. It contains lidocaine, which provides temporary relief from pain and itching, making it helpful for sunburns, minor burns, cuts, scrapes, and insect bites.

This gel not only helps to soothe the skin but also offers comfort during the healing process. With a net weight of 8 oz (227 g), it’s a convenient option to have on hand for those times when your skin needs extra care.

Uses

You can use this medication for temporary relief of pain and itching. It is particularly helpful in soothing discomfort from sunburn, minor burns, cuts, scrapes, skin irritations, and insect bites. Whether you're dealing with a pesky bug bite or a minor burn, this product can provide the relief you need to feel more comfortable.

Dosage and Administration

If you are an adult or a child aged 2 years and 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 safe and effective use.

However, if you have a child under 2 years of age, it’s important not to use this medication without consulting a doctor first. Always prioritize safety and seek professional advice when it comes to younger children.

What to Avoid

It's important to use this medication responsibly. You should avoid using it in large quantities, especially on raw surfaces or blistered areas, as this can lead to complications. While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this medication, always follow the recommended guidelines to ensure your safety and well-being. If you have any questions or concerns, don't hesitate to reach out to your healthcare provider for more information.

Side Effects

This product is intended for external use only, so please avoid applying it in large amounts, especially on raw or blistered skin. While using it, be careful not to let it come into contact with your eyes.

If your condition worsens or if symptoms last longer than 7 days, you should stop using the product and consult a doctor. Additionally, if your symptoms improve and then return within a few days, it's important to seek medical advice. Always keep this product out of reach of children, and if it is swallowed, seek medical help or contact the Poison Control Center right away.

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 to keep it away from your eyes, as contact can cause irritation.

If your condition worsens or does not improve after 7 days of use, or if your symptoms clear up and then return within a few days, stop using the product and consult your doctor. It's also important to keep this product out of reach of children. If it is swallowed, seek medical help or contact the Poison Control Center right away.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help right away. You can contact your local Poison Control Center for guidance. They can provide you with the necessary steps to take in this situation.

Signs of an overdose can vary, but it’s crucial to be aware of any unusual symptoms that may arise. If you notice anything concerning, don’t hesitate to reach out for help immediately. Your safety is the top priority, so acting quickly can make a significant difference.

Pregnancy Use

It’s important to be cautious when considering any medication during pregnancy. In the case of Publix Burn Relief (lidocaine hcl gel), there is currently no information available about its safety, recommended dosage adjustments, or any special precautions for use during pregnancy.

If you are pregnant or planning to become pregnant, it’s best to consult with your healthcare provider before using this product or any medication. They can help you understand the potential risks and make informed decisions for your health and the health of your baby.

Lactation Use

If you are breastfeeding, it's important to be cautious when considering the use of this product, as it may be excreted in breast milk (meaning it can pass into your milk and potentially affect your baby). To ensure the safety of both you and your nursing infant, it is highly recommended that you consult with your healthcare provider before using this product. They can provide personalized advice based on your specific situation.

Pediatric Use

If your child is under 2 years old, it's important not to use this medication without consulting a doctor first. For children aged 2 years and older, you can apply the medication to the affected area, but make sure to do so no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

When considering the use of Publix Burn Relief (lidocaine hcl gel) for older adults, it's important to note that the drug insert does not provide specific information about dosage adjustments, safety concerns, or special precautions for elderly patients. This means that while the product may be used, there are no established guidelines tailored for older adults.

If you are caring for an older adult, it's wise to consult with a healthcare professional before using this product. They can help ensure that it is appropriate and safe based on individual health needs and any other medications being taken.

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 or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, discussing your full list of medications and any tests you undergo ensures that your healthcare provider can help you avoid potential issues and provide the best care tailored to your needs. Always feel free to ask questions and share your concerns during your appointments.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature, away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination. Once you open the container, be sure to discard it after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged 2 years and 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 Publix Burn Relief ALOE VERA GEL used for?

It provides temporary relief of pain and itching from sunburn, minor burns, cuts, scrapes, skin irritations, and insect bites.

How should I use Publix Burn Relief ALOE VERA GEL?

Apply to the affected area not more than 3 to 4 times daily for adults and children 2 years of age and older. Do not use in large quantities, especially over raw surfaces or blistered areas.

Are there any age restrictions for using this product?

Do not use this product on children under 2 years of age without consulting a doctor.

What should I do if my condition worsens or symptoms persist?

Stop use and ask a doctor if your condition worsens or if symptoms persist for more than 7 days.

Is there any information regarding use during pregnancy?

There is no specific information regarding the safety or use of this product during pregnancy.

Can nursing mothers use this product?

Nursing mothers should exercise caution when using this product and consult a healthcare provider, as it may be excreted in breast milk.

What should I do if the product is swallowed?

Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center immediately.

How should I store Publix Burn Relief ALOE VERA GEL?

Store at room temperature, protect from light, and keep the container tightly closed. Discard after opening.

Are there any contraindications for this product?

No contraindications are specified for Publix Burn Relief ALOE VERA GEL.

Is this product safe for external use?

Yes, it is for external use only. Avoid contact with eyes when using this product.

Packaging Info

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

Packaging configurations for Publix Burn Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Publix Burn Relief Aloe Vera Gel is formulated to cool and relieve sunburn pain. It contains lidocaine as an active ingredient, enhancing its soothing properties. The product is presented in a net weight of 8 ounces (227 grams).

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with various dermatological conditions. It helps relieve and soothe pain from sunburn, minor burns, cuts, scrapes, skin irritations, and insect bites.

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 limited to the specified frequency to avoid potential adverse effects.

For children under 2 years of age, the product should not be used unless directed by a healthcare professional. In such cases, it is advisable to consult a doctor for appropriate guidance.

Contraindications

Use is contraindicated in patients who may apply the product in large quantities, particularly over raw surfaces or blistered areas, due to the potential for adverse effects in these conditions. No other specific contraindications have been identified.

Warnings and Precautions

For external use only. This product should not be 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 during application. In the event of accidental contact, it is advisable to rinse thoroughly with water.

Healthcare professionals should instruct patients to discontinue use and seek medical advice if the condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms resolve and then recur within a few days, medical consultation is recommended.

It is essential to keep this product out of reach of children. In cases of ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

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 blistered areas. During use, contact with the eyes should be strictly avoided.

In the event that the condition worsens or symptoms persist for more than 7 days, patients are advised to stop use and consult a doctor. Additionally, if symptoms clear up and then recur within a few days, medical advice should be sought.

This product should be kept out of reach of children. If swallowed, it is imperative to seek medical help or contact a Poison Control Center immediately.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Publix Burn Relief.
Details

Pediatric Use

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

Geriatric Use

There is no specific information regarding the use of Publix Burn Relief (lidocaine hcl gel) in geriatric patients. The prescribing information does not indicate any dosage adjustments, safety concerns, or special precautions that are specifically applicable to elderly patients. Therefore, healthcare providers should exercise clinical judgment when considering the use of this medication in geriatric populations, as individual patient factors may influence treatment decisions. Monitoring for efficacy and potential adverse effects is recommended, as with any medication administered to elderly patients.

Pregnancy

There is currently no information available regarding the use of Publix Burn Relief (lidocaine hcl gel) during pregnancy. This includes any safety concerns, dosage modifications, or special precautions that may be necessary for pregnant patients. Healthcare professionals should consider the lack of data when advising women of childbearing potential and weigh the potential risks and benefits before recommending this product during pregnancy.

Lactation

Lactating mothers should exercise caution when using this product due to the potential for excretion in breast milk. It is recommended that they consult a healthcare provider before using this product while breastfeeding.

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, it is imperative that immediate medical assistance is sought. Healthcare professionals should advise patients or caregivers to contact a Poison Control Center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential. Prompt recognition of symptoms can facilitate timely intervention and management.

Management of overdosage should be guided by the clinical presentation and may include supportive care and symptomatic treatment. Healthcare providers are encouraged to follow established protocols for the management of overdose cases, which may involve activated charcoal administration, intravenous fluids, or other interventions as deemed necessary based on the patient's condition.

In all cases of suspected overdosage, the involvement of poison control and emergency medical services is crucial to ensure optimal patient outcomes.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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 of swallowing the product, patients should seek medical help or contact the Poison Control Center immediately.

Patients should be informed not to use the product in large quantities, especially over raw surfaces or blistered areas, as this may lead to adverse effects. They should also be instructed to stop use and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, patients should be made aware that if symptoms improve and then recur within a few days, they should discontinue use and seek medical advice.

It is important to remind patients to avoid contact with their eyes while using this product to prevent irritation or injury.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3 to 4 times daily for adults and children aged 2 years and older. For children under 2 years of age, it is advised to consult a doctor before use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Publix 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 Publix 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.