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Burn Relief Aloe

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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)
Marketed in the U.S.
Since 2016
Label revision date
May 14, 2018
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
Marketed in the U.S.
Since 2016
Label revision date
May 14, 2018
Manufacturer
Rite Aid
Registration number
part348
NDC root
11822-7782

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Drug Overview

You can use this medication for temporary relief of pain and itching caused by various skin irritations, including sunburn, minor burns, insect bites, cuts, and scrapes. It helps soothe discomfort and promotes a sense of relief, allowing you to feel more comfortable while your skin heals.

Uses

You can use this medication for the temporary relief of pain and itching caused by various skin irritations. It is effective for soothing discomfort from sunburn, minor burns, insect bites, cuts, and scrapes.

This product is designed to help you feel more comfortable when dealing with these common skin issues, allowing you to get back to your daily activities with less irritation.

Dosage and Administration

If you or your child is 2 years old or older and need to use this medication, you should apply it directly to the affected area. You can do this up to 3 to 4 times a day, but make sure not to exceed this amount.

For children under 2 years of age, it's important to consult a physician (doctor) before using the medication to ensure it's safe and appropriate for them. Always follow these guidelines to help ensure effective and safe use of the medication.

What to Avoid

It's important to be aware of certain guidelines when using this medication. If your symptoms persist for more than 7 days, you should stop using the product and consult your doctor for further advice. Additionally, be careful to avoid contact with your eyes; if this happens, rinse your eyes with water immediately.

While there are no specific contraindications, controlled substance classifications, or noted risks of abuse or dependence associated with this medication, following these precautions will help ensure your safety and well-being.

Side Effects

This product is intended for external use only, so it's important to avoid getting it in your eyes. If contact does occur, rinse your eyes with water immediately.

If your symptoms persist for more than 7 days while using this product, you should stop using it and consult a doctor for further advice.

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to any internal areas. Be careful to keep it away from your eyes; if it does come into contact with them, rinse thoroughly with water.

If you notice that your symptoms persist for more than 7 days while using this product, it’s important to stop using it and consult your doctor for further advice. Your health and safety are paramount, so don’t hesitate to seek help if you have any concerns.

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 signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's always better to be safe and get checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Pregnancy Use

When it comes to using BURN RELIEF ALOE DAYLOGIC (lidocaine hydrochloride 0.5% gel) during pregnancy, there is currently no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that the effects of this product on pregnant individuals and their developing babies are not well-studied or documented.

If you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before using this product. They can help you weigh the potential risks and benefits based on your individual situation. Always prioritize your health and the health of your baby when considering any medication.

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. This means you can use the product without worrying about its effects on your milk production or your baby's health. Always consult with your healthcare provider if you have any questions or concerns about your specific situation.

Pediatric Use

When using this medication for children aged 2 years and older, you should apply it to the affected area no more than 3 to 4 times a day. If your child is under 2 years old, it's important to consult a physician (doctor) before using the medication to ensure it's safe for them. Always follow these guidelines to help keep your child safe and healthy.

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 since older adults may have different health needs and may be taking other medications.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health conditions and overall treatment goals. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

Renal Impairment

There are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for patients with kidney problems in the provided information. If you have renal impairment (kidney issues), it's important to consult your healthcare provider for personalized advice and to ensure your treatment is safe and effective. Always keep your doctor informed about your kidney health, as they may need to adjust your medications or monitor you more closely.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines, dosage adjustments, or special monitoring instructions provided for your condition in the available information. This means that the medication may not have been studied in depth for its effects on individuals with liver impairment.

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 your treatment is safe and effective based on your individual health needs.

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 way, you can work together to ensure your treatment is safe and effective.

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 to 77°F). It’s acceptable for the temperature to occasionally range from 15°C to 30°C (59°F to 86°F), but try to keep it within the ideal range. Make sure to protect the product from light and always keep the container tightly closed when not in use.

Once you open the container, remember to discard any remaining product, as it should not be reused. Following these guidelines will help maintain the safety and effectiveness of the product.

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 the patient is under 2 years old, it's important to consult a physician before use. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is this product used for?

This product is used for the temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts, and scrapes.

How should I apply this product?

For adults and children 2 years of age and older, apply to the affected area no more than 3 to 4 times a day. For children under 2 years of age, consult a physician.

Are there any warnings I should be aware of?

This product is for external use only. Avoid contact with eyes, and rinse with water if contact occurs.

What should I do if symptoms last more than 7 days?

You should stop using the product and ask a doctor if symptoms last more than 7 days.

Is this product safe to use during pregnancy or while nursing?

There is no specific information regarding the use of this product during pregnancy or lactation, so consult a physician for advice.

How should I store this product?

Store at 20°C to 25°C (68°F to 77°F), protect from light, and keep the container tightly closed. Discard after opening.

Are there any contraindications for this product?

No contraindications are listed for this product.

What should I do if I accidentally get this product in my eyes?

If contact with eyes occurs, rinse with water immediately.

Packaging Info

Below are the non-prescription pack sizes of Burn Relief Aloe (lidocaine hydrochloride 0.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Burn Relief Aloe.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available data.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with sunburn, minor burns, insect bites, cuts, and scrapes.

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 exceeding 3 to 4 times per day. It is essential to ensure that the application is performed with clean hands and that the affected area is clean and dry prior to administration.

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

Contraindications

There are no specific contraindications listed for this product. However, it is advised to discontinue use and consult a healthcare professional if symptoms persist for more than 7 days. Additionally, avoid contact with the eyes; in the event of contact, rinse thoroughly with water.

Warnings and Precautions

This product is intended for external use only. Healthcare professionals should advise patients to avoid contact with the eyes during application. In the event of accidental eye contact, it is imperative to rinse the eyes thoroughly with water.

Patients should be instructed to discontinue use and consult a healthcare provider if symptoms persist for more than 7 days. This precaution is essential to ensure appropriate evaluation and management of any underlying conditions that may require further medical attention.

Side Effects

Patients should be aware that this product is for external use only. It is important to avoid contact with the eyes; in the event of contact, the affected area should be rinsed with water immediately.

In clinical practice, patients are advised to discontinue use and consult a healthcare professional if symptoms persist for more than 7 days. This precaution is essential to ensure appropriate management and to rule out any underlying conditions that may require further evaluation.

Drug Interactions

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

Packaging & NDC

Below are the non-prescription pack sizes of Burn Relief Aloe (lidocaine hydrochloride 0.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Burn Relief Aloe.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area up to 3 to 4 times daily. For infants and children under 2 years of age, it is recommended to consult a physician prior to use.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

There is no specific information available regarding the use of BURN RELIEF ALOE DAYLOGIC (lidocaine hydrochloride 0.5% gel) during pregnancy. As such, the safety of this medication in pregnant patients has not been established, and there are no known dosage modifications or special precautions recommended for use during pregnancy. Healthcare professionals should weigh the potential benefits against any unknown risks when considering this medication for women of childbearing potential. Further studies may be necessary to fully understand the implications of lidocaine hydrochloride use in this population.

Lactation

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

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

Hepatic Impairment

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise caution and consider the lack of data when prescribing this medication to patients with liver problems.

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, as the clinical presentation can vary depending on the substance involved and the individual patient's response. Common symptoms of overdose may include, but are not limited to, altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and ensuring adequate circulation. The use of activated charcoal may be considered if the patient presents within a suitable timeframe and is deemed appropriate based on clinical judgment.

Additionally, specific antidotes or treatments may be indicated depending on the substance involved in the overdose. Consultation with a poison control center or a medical toxicologist is recommended for guidance on the most effective management strategies.

Overall, vigilance and prompt intervention are critical in managing cases of suspected overdose to mitigate potential complications and ensure patient safety.

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 provided text.

Patient Counseling

Healthcare providers should advise patients to seek medical attention if their symptoms persist for more than 7 days. It is important for patients to understand that prolonged symptoms may indicate a need for further evaluation and management.

Additionally, healthcare providers should instruct patients to avoid contact with their eyes while using the medication. In the event of accidental contact, patients should be informed to rinse their eyes thoroughly with water to mitigate any potential irritation or adverse effects.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain integrity. It should be stored at a temperature range of 20°C to 25°C (68°F to 77°F), with permissible excursions between 15°C to 30°C (59°F to 86°F). It is essential to protect the product from light to prevent degradation. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with the recommended application frequency for adults and children aged 2 years and older being 3 to 4 times per day to the affected area. For children under 2 years of age, it is advised to consult a physician prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

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

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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.