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Aramark Burn Gel

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This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 20 mg/1 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 2021
Label revision date
September 9, 2021
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 20 mg/1 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 2021
Label revision date
September 9, 2021
Manufacturer
Western First Aid Safety DBA Aramark
Registration number
part348
NDC root
81238-5000
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 is a product designed to provide temporary pain relief for minor burns. It is specifically formulated to help soothe discomfort associated with these types of injuries. This gel is intended for professional use, ensuring that it is applied correctly and effectively to assist in the healing process.

Uses

You can use this medication for temporary pain relief if you have minor burns. It's important to note that this product is intended for professional use only, so make sure to consult with a healthcare provider for proper application and guidance.

Additionally, there are no concerns regarding teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this medication. Always prioritize safety and seek professional advice when dealing with burns or any other medical concerns.

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 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 medication safely to avoid any potential issues. You should not apply it in large amounts, especially on raw or blistered skin, as this can lead to irritation or other complications. Additionally, be careful not to use it near your eyes; if it accidentally comes into contact with your eyes, rinse them thoroughly with water to prevent discomfort.

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 the treatment.

Side Effects

This product is intended for external use only. It's important to avoid using it in large amounts, especially on raw or blistered skin, and to keep it away from your eyes. If the product accidentally gets into your eyes, rinse them thoroughly with water.

You should stop using the product and consult a doctor if your condition worsens, if symptoms last longer than 7 days, or if they seem to improve and then return within a few days.

Warnings and Precautions

This product is intended for external use only, so please keep it out of reach of children. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately.

Be cautious when applying the product; avoid using large amounts, especially on raw or blistered skin, and keep it away from your eyes. If the product does come into contact with your eyes, rinse them thoroughly with water. If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult your doctor.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, 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

There is currently no specific information available about the use of ARAMARK BURN GEL (lidocaine gel) during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product. They can help you understand any potential risks and make informed decisions about your care.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your doctor before using this product. There is a possibility that it may be excreted in breast milk, which means it could potentially affect your baby. Since the effects on nursing infants have not been thoroughly studied, it's best to exercise caution. Always prioritize your health and your baby's well-being by discussing any concerns with your healthcare provider.

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 it comes to using ARAMARK BURN GEL, there is no specific information available about how it should be used by older adults. This means that there are no special dosage adjustments or safety concerns outlined for elderly patients. However, it’s always important to consult with a healthcare provider before using any new medication or treatment, especially if you or your loved ones are older adults. They can provide personalized advice and ensure that the product is safe and appropriate for your specific health needs.

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 for patients with 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 if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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 changes in your medications or upcoming lab tests with your healthcare provider to avoid any potential issues and to get the best care possible.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and avoid freezing it. It's important to keep the product in its original packaging and never use any packets that are open or torn, as this can compromise safety and effectiveness. By following these simple guidelines, you can help maintain the quality and reliability of the device.

Additional Information

No further information is available.

FAQ

What is Burn Gel used for?

Burn Gel is used for temporary pain relief of minor burns.

Who can use Burn Gel?

Burn Gel is for professional use only and can be applied by adults and children 2 years of age and older.

How often can I apply Burn Gel?

You can apply Burn Gel to the affected area not more than 3 to 4 times daily.

Is Burn Gel safe for children under 2 years?

No, do not use Burn Gel on children under 2 years; consult a doctor instead.

Are there any contraindications for using Burn Gel?

No specific contraindications are mentioned for Burn Gel.

What should I do if I accidentally get Burn Gel in my eyes?

If Burn Gel gets in your eyes, rinse thoroughly with water.

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

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

Can nursing mothers use Burn Gel?

Nursing mothers should consult a doctor before using Burn Gel, as there is a potential for excretion in breast milk.

How should I store Burn Gel?

Store Burn Gel at room temperature and do not freeze. Do not use any open or torn packets.

Packaging Info

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

Packaging configurations for Aramark Burn Gel.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

BURN GEL is indicated for the temporary relief of pain associated with minor burns. Each packet contains 0.9 grams of the product, with a total count of 25 packets per carton. BURN GEL is manufactured by Aramark, located in Lenexa, Kansas, 66219. For further information, the manufacturer can be contacted at 886-362-2691 or through their website at aramarkuniform.com. It is advised to retain the carton for drug information.

Uses and Indications

This drug is indicated for the temporary relief of pain associated with minor burns. It is intended for professional use only.

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 without consulting a healthcare professional. It is essential to seek medical advice before administering this treatment to this age group.

Contraindications

The product should not be applied in large quantities, especially over raw or blistered areas, due to the potential for irritation or adverse effects. Additionally, application near the eyes is contraindicated; in the event of contact, the area should be rinsed thoroughly with water to mitigate any potential harm.

Warnings and Precautions

For external use only. It is imperative to keep this product out of reach of children to prevent accidental ingestion. In the event of swallowing, immediate medical assistance should be sought, or contact a Poison Control Center directly.

Caution is advised regarding the application of this product. It should not be used in large quantities, especially over raw or blistered areas, as this may exacerbate the condition. Additionally, care must be taken to avoid contact with the eyes. Should contact occur, the affected area should be rinsed thoroughly with water.

Healthcare professionals should advise patients to discontinue use and consult a doctor if the condition worsens or if symptoms persist for more than 7 days. Patients should also be informed to seek medical advice if symptoms resolve and then recur within a few days.

Side Effects

For external use only. Patients are advised not to use the product in large quantities, particularly over raw or blistered areas, and to avoid contact with the eyes. In the event of accidental contact with the eyes, it is recommended to rinse thoroughly with water.

Patients should discontinue use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then occur again within a few days.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

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

Packaging configurations for Aramark Burn Gel.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this medication and must consult a healthcare professional for guidance. 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 ARAMARK BURN GEL in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when administering this product to elderly patients, as individual responses may vary. Monitoring for any adverse effects or complications is advisable, given the lack of targeted data for this population.

Pregnancy

There is no specific information regarding the use of ARAMARK BURN GEL (lidocaine gel) during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in pregnant women, as the potential risks and effects on fetal outcomes are not well characterized. It is advisable to weigh the benefits against any unknown risks when prescribing this medication to women of childbearing potential.

Lactation

Nursing mothers are advised to consult a doctor before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are not well studied; therefore, caution is advised when considering the use of this product during lactation.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the event of an overdosage, immediate medical assistance is essential. Healthcare professionals are advised to seek medical help or contact a Poison Control Center if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved. It is crucial for healthcare providers to assess the patient's condition and monitor for any adverse effects that may arise from the overdose.

Management of overdosage should be guided by the clinical presentation and the specific substance involved. Supportive care and symptomatic treatment are often necessary. In cases of ingestion, activated charcoal may be considered if appropriate and within the recommended time frame. Continuous monitoring of vital signs and supportive measures should be implemented as needed.

Prompt recognition and intervention are vital to mitigate potential complications associated with overdosage.

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 use of the compound in these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. In the event that the medication is swallowed, patients should be instructed to seek medical help immediately or contact a Poison Control Center for guidance. It is important for patients to understand the potential risks associated with improper use and the necessary steps to take in case of an emergency.

Storage and Handling

The product is supplied in packets that must be stored at room temperature. It is essential to avoid freezing the product to maintain its integrity. Healthcare professionals should ensure that only intact packets are used, as any open or torn packets should not be utilized.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Aramark Burn Gel, 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 Aramark Burn Gel, 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.