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Rite Aid Burn Relief

Last content change checked dailysee data sync status

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 2012
Label revision date
December 3, 2012
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 2012
Label revision date
December 3, 2012
Manufacturer
RITE AID CORPORATION
Registration number
part348
NDC root
11822-9009

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Drug Overview

Rite Aid 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. This gel is effective for soothing discomfort from sunburn, minor burns, cuts, scrapes, and insect bites, helping to promote a more comfortable healing process.

With a net weight of 8 ounces (227 grams), this product is easy to apply and can be a helpful addition to your first aid supplies for treating various skin issues.

Uses

You can use this medication for temporary relief from pain and itching. It is particularly helpful for soothing discomfort caused by 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 the best results.

However, if your child is under 2 years old, 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 safely. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately. If your condition worsens or symptoms last longer than seven days, stop using the medication and consult your doctor. Additionally, if your symptoms improve but then return within a few days, you should also reach out to your healthcare provider.

Be sure to avoid contact with your eyes while using this medication to prevent irritation or injury. Always follow these guidelines to ensure your safety and well-being.

Side Effects

When using this product, it's important to apply it only to the skin and avoid using large amounts, especially on broken or blistered skin. Be careful to keep it away from your eyes. If your condition worsens or does not improve after a week, or if symptoms improve and then return shortly after, you should stop using the product and consult a doctor.

Additionally, keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

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 to prevent irritation.

If you notice that your condition worsens or if your symptoms last longer than 7 days, it's important to stop using the product and consult your doctor. Additionally, if your symptoms improve but then return within a few days, you should also reach out to your healthcare provider. In the event that the product is swallowed, seek medical help immediately or contact a Poison Control Center for assistance.

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 require prompt attention. Always err on the side of caution and get help if you suspect an overdose has occurred. Your health and safety are the top priority.

Pregnancy Use

There is currently no specific information available regarding the use of RITE AID BURN RELIEF - lidocaine hydrochloride 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 to ensure it is safe for you and your baby. Always prioritize open communication with your doctor about any medications you are considering during pregnancy.

Lactation Use

If you are breastfeeding and considering using RITE AID BURN RELIEF, which contains lidocaine hydrochloride gel, it's important to note that the drug insert does not provide specific information about its use in nursing mothers or any potential effects on breastfeeding. This means that there is no clear guidance on how this medication may affect your milk production or your nursing infant.

As always, it's best to consult with your healthcare provider before using any medication while breastfeeding. They can help you weigh the benefits and risks based on your individual situation.

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 to 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 prioritize your child's safety and seek professional advice if you're unsure.

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 or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature and keep it 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 any remaining product after use to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is RITE AID BURN RELIEF ALOE VERA GEL used for?

RITE AID BURN RELIEF ALOE VERA GEL is used for temporary pain relief of pain and itching, helping to soothe pain from sunburn, minor burns, cuts, scrapes, skin irritations, and insect bites.

How should I apply RITE AID BURN RELIEF ALOE VERA GEL?

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

Are there any warnings I should be aware of?

This product is for external use only. Avoid contact with eyes and do not use in large quantities, especially over raw surfaces or blistered areas.

What should I do if I swallow RITE AID BURN RELIEF ALOE VERA GEL?

If swallowed, get medical help or contact a Poison Control Center right away.

What should I do if my symptoms worsen or persist?

Stop use and ask a doctor if conditions worsen or if symptoms persist for more than 7 days, or if symptoms clear up and occur again within a few days.

How should I store RITE AID 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 using this product?

No contraindications are listed for RITE AID BURN RELIEF ALOE VERA GEL.

Is RITE AID BURN RELIEF ALOE VERA GEL safe to use during pregnancy or while nursing?

No specific information regarding safety during pregnancy or nursing is provided in the drug insert.

Packaging Info

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

Packaging configurations for Rite Aid Burn Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Rite Aid Burn Relief Aloe Vera Gel is formulated to provide cooling and relief from sunburn pain through the inclusion of lidocaine. This product is presented in a dosage form of a gel and is packaged 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 to soothe and alleviate discomfort resulting 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, consultation with a doctor is advised prior to use.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that medical assistance be sought immediately if the product is swallowed. Additionally, healthcare professionals should instruct patients to discontinue use and consult a doctor if conditions worsen or if symptoms persist for more than 7 days. Patients should also be advised to stop use and seek medical advice if symptoms resolve and then recur within a few days. Care should be taken to avoid contact with the eyes.

Warnings and Precautions

This product is intended for external use only. It is imperative that users refrain from applying it 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, immediate rinsing with water is recommended.

Users are advised to discontinue use and consult a healthcare professional if any of the following occur: the condition worsens, symptoms persist for more than 7 days, or if symptoms resolve and then reappear within a few days. These actions are crucial to ensure the safety and efficacy of the treatment.

In cases of ingestion, it is essential to seek medical assistance or contact a Poison Control Center immediately. Prompt action is necessary to address any potential complications arising from accidental swallowing.

Side Effects

Patients using this product should be aware that it is intended for external use only and should not be applied in large quantities, particularly over raw surfaces or blistered areas. Contact with the eyes should be avoided to prevent irritation.

In clinical practice, patients are advised to discontinue use and consult a healthcare professional if their condition worsens or if symptoms persist for more than 7 days. Additionally, if symptoms resolve and then recur within a few days, it is recommended to seek medical advice.

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

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Rite Aid Burn Relief.
Details

Pediatric Use

Pediatric patients aged 2 years and older may 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.

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 regarding the use of RITE AID BURN RELIEF - lidocaine hydrochloride 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 benefits have not been established. It is advisable to weigh the necessity of treatment against the lack of data on fetal outcomes and to consider alternative therapies when appropriate.

Lactation

There is no specific information regarding nursing mothers or lactation considerations provided in the drug insert for RITE AID BURN RELIEF - lidocaine hydrochloride gel. Therefore, the effects on breastfed infants and the excretion of lidocaine hydrochloride in breast milk are not established. Healthcare professionals should exercise caution and consider the potential risks versus benefits when recommending this product to lactating mothers.

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 assistance is crucial. Healthcare professionals are advised to seek medical help or 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 of the patient's condition is essential. Prompt recognition of symptoms can facilitate timely intervention and management.

Management procedures should include supportive care and symptomatic treatment as necessary. Continuous monitoring of the patient's vital signs and clinical status is recommended to address any complications that may arise during the course of treatment.

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 seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important for patients to understand the necessity of stopping the use of the product and consulting a doctor if their condition worsens or if symptoms persist for more than seven days. Additionally, patients should be informed to discontinue use and consult a healthcare professional if symptoms resolve but then reoccur within a few days.

Providers should also emphasize the importance of avoiding contact with the eyes while using this product, as this could lead to adverse effects. Clear communication of these points will help ensure patient safety and effective use of the product.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which should be referenced for accurate identification. It is essential to store the product at room temperature to maintain its integrity. The container must be kept tightly closed to prevent contamination and degradation. Additionally, the product should be protected from light exposure to ensure optimal stability. Once opened, the product must be discarded to avoid any potential safety risks.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Rite Aid 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 Rite Aid 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.

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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.