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Aramark Burn Cream

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredients
  • Lidocaine Hydrochloride 5 mg/1 g
  • Benzalkonium Chloride 1.3 mg/1 g
Other brand names
Dosage form
Cream
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
May 21, 2021
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Lidocaine Hydrochloride 5 mg/1 g
  • Benzalkonium Chloride 1.3 mg/1 g
Other brand names
Dosage form
Cream
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
May 21, 2021
Manufacturer
Western First Aid Safety dba Aramark
Registration number
part348
NDC root
81238-4622
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

Aramark is a first aid and burn cream designed to provide temporary relief from pain associated with minor cuts, scrapes, and burns. It acts as both an antiseptic, helping to protect against harmful bacteria, and an anesthetic, soothing the affected area to alleviate discomfort. This cream comes in convenient 1g packets, making it easy to apply when you need it most.

By using Aramark, you can help protect your skin from infection while also relieving pain and promoting healing. It's a practical option to keep on hand for minor injuries, ensuring you have the support you need for everyday mishaps.

Uses

You can use this product for the temporary relief of pain caused by minor cuts, scrapes, and burns. It also helps protect your skin from harmful bacteria, which can prevent infections and promote healing.

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

Dosage and Administration

To use this medication effectively, start by cleaning the affected area thoroughly. Once it's clean, apply a small amount of the medication. You should do this no more than three times a day. If you prefer, you can cover the area with a sterile bandage (a clean, protective covering) after applying the medication to help keep it clean and promote healing.

What to Avoid

It's important to keep this medication out of reach of children to prevent accidental ingestion. If you or someone else accidentally takes it, please contact a Poison Control Center immediately for assistance.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always use it responsibly and follow any additional guidance provided by your healthcare professional.

Side Effects

It's important to use this product only on the skin and avoid contact with your eyes. You should not apply it in large amounts or on areas that are raw, blistered, or have deep puncture wounds, animal bites, or serious burns. Additionally, do not use it for more than one week unless your doctor advises you to do so.

If you experience any unusual reactions or side effects, please consult your healthcare provider for guidance.

Warnings and Precautions

This product is for external use only, so please avoid using it in your eyes or applying it in large amounts. Do not use it on raw or blistered skin, deep puncture wounds, animal bites, or serious burns. It's important to limit use to no more than one week unless your doctor advises otherwise.

If you experience any unusual reactions or if your condition worsens, stop using the product and contact your doctor for further guidance. Always prioritize your safety and well-being when using any medication.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe you have taken too much of the medication, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get checked out if you have any concerns about your health.

Pregnancy Use

There is currently no specific information available regarding the use of ARAMARK BURN CREAM 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 cream. They can provide guidance based on your individual health needs and circumstances.

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

It's important to keep this medication out of reach of children. If a child accidentally ingests it, you should contact a Poison Control Center immediately for guidance. Taking quick action can help ensure their safety. Always be vigilant and store medications securely to prevent any accidental exposure.

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 if you or a loved one is an older adult considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

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 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.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This helps to avoid any potential issues and ensures that you receive the best possible treatment tailored to your needs.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. It's important to keep it out of reach of children to prevent any accidental ingestion or misuse. Once you open the product, be sure to discard it after use to maintain safety and hygiene. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically, using a small amount no more than three times a day. It's important to follow this guideline to ensure safe and effective use. If you have any questions about how to use the medication or its effects, be sure to consult your healthcare provider for more information.

FAQ

What is aramark used for?

Aramark is a first aid/burn cream used for the temporary relief of pain associated with minor cuts, scrapes, and burns, while also helping to protect against harmful bacteria.

How should I apply aramark?

Clean the affected area and apply a small amount of aramark not more than 3 times daily. It may be covered with a sterile bandage.

Are there any contraindications for using aramark?

There are no specific contraindications listed for aramark.

What precautions should I take when using aramark?

Use aramark for external use only. Avoid using it in the eyes, in large quantities, over raw or blistered areas, or on deep puncture wounds, animal bites, or serious burns.

What should I do if I accidentally ingest aramark?

If ingested, contact a Poison Control Center immediately.

Is aramark safe to use during pregnancy or while nursing?

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

How should I store aramark?

Store aramark at room temperature and keep it out of reach of children. Discard after opening.

Packaging Info

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

Packaging configurations for Aramark Burn Cream.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Aramark is a first aid and burn cream available in packets containing 1 gram each, with a total of 25 packets per carton. This formulation serves as an antiseptic and anesthetic, providing pain relief, soothing properties, and protection against infection. The product is designed for easy access, with a removable top for convenience. It is comparable to Johnson & Johnson First Aid Cream. For complete product information, the carton should be retained. The cream is manufactured by Aramark, located in Lenexa, KS 66219, and can be contacted at (913) 269-9611.

Uses and Indications

This drug is indicated for the temporary relief of pain associated with minor cuts, scrapes, and burns. Additionally, it helps protect against harmful bacteria, contributing to the overall management of minor skin injuries.

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

Dosage and Administration

The affected area should be cleaned thoroughly prior to application. A small amount of the medication should be applied to the affected area, not exceeding three times daily. If desired, the area may be covered with a sterile bandage following application to protect the site.

Contraindications

There are no specific contraindications listed for this product. However, it is essential to keep the product out of reach of children. In the event of ingestion, immediate contact with a Poison Control Center is advised to ensure appropriate management and care.

Warnings and Precautions

For external use only. This product should not be applied in or around the eyes. It is contraindicated for use in large quantities and should not be used over raw or blistered areas, on deep puncture wounds, animal bites, or serious burns. The duration of use should not exceed one week unless directed by a healthcare professional.

Healthcare providers should ensure that patients are aware of these warnings to prevent misuse and potential complications. Monitoring for adverse reactions is advised, particularly in patients who may inadvertently apply the product inappropriately or exceed the recommended duration of use.

Side Effects

Patients should be aware that the product is intended for external use only. It is contraindicated for use in the eyes and should not be applied in large quantities. Additionally, the product should not be used over raw or blistered areas, on deep puncture wounds, animal bites, or serious burns. Prolonged use beyond one week is not recommended unless directed by a healthcare professional.

While specific adverse reactions have not been detailed, the warnings indicate potential risks associated with improper use. Patients are advised to adhere strictly to the guidelines provided to minimize the risk of adverse effects.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Aramark Burn Cream.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of ingestion, it is crucial to contact a Poison Control Center immediately for guidance.

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.

Pregnancy

There is no specific information regarding the use of ARAMARK BURN CREAM during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in the absence of established safety profiles for this population. Women of childbearing potential should be counseled accordingly.

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 absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the amount and timing of the substance taken, is crucial for effective treatment and follow-up care.

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 medication out of reach of children to prevent accidental ingestion. In the event of ingestion, it is crucial for patients to contact a Poison Control Center immediately for guidance and assistance.

Storage and Handling

The product is supplied in a configuration that ensures optimal usability. It should be stored at room temperature to maintain its integrity and effectiveness. It is essential to keep the product out of reach of children to prevent accidental ingestion. Once opened, the product must be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application of a small amount not exceeding three times daily. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

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