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Aloe Gel Pain Reliever

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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 2013
Label revision date
February 12, 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 2013
Label revision date
February 12, 2018
Manufacturer
Walgreens
Registration number
part348
NDC root
0363-3192

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Drug Overview

This medication is designed to provide temporary relief from pain and itching caused by various skin irritations, including sunburn, minor burns, insect bites, cuts, and scrapes. It works by soothing the affected area, helping to alleviate discomfort and promote healing.

If you are experiencing any of these skin issues, this drug may help ease your symptoms and improve your comfort. Always consult with a healthcare professional for personalized advice and treatment options.

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 or concerns regarding abuse, misuse, or dependence associated with this medication, following these instructions will help ensure your safety and well-being.

Side Effects

This product is intended for external use only, so it's important to avoid contact with your eyes. If you accidentally get it in your eyes, rinse them 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, or if you are unsure, 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

There is currently no information available about the use of ALOE GEL PAIN RELIEVER WELL AT WALGREENS (lidocaine hydrochloride 0.5% 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 regarding any medications you may consider during this time.

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 is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If your child is 2 years old or older, you can apply the medication to the affected area up to 3 to 4 times a day. However, if your child is under 2 years of age, it's important to consult a physician (doctor) before using this medication. Always follow these guidelines to ensure your child's safety and well-being.

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, it’s important to consult with a healthcare provider for personalized advice. 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 there are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for your condition in the provided information. This means that the standard recommendations for medication use may apply to you without any special considerations. However, always consult your healthcare provider for personalized advice and to ensure your treatment is safe and effective based on your kidney health.

Hepatic Impairment

If you have liver 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 standard recommendations apply, and there are no special monitoring or precautions outlined for patients with liver impairment.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe for your liver health. They can provide guidance based on your individual situation and help monitor your liver function as needed.

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 any other medications or supplements you may be using. Your safety and well-being are the top priority, and discussing your full health picture helps your provider support you best.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20°C to 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 recommended limits. 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 the drug indicated for?

The drug is indicated for temporary relief of pain and itching due to sunburn, minor burns, insect bites, cuts, and scrapes.

How should I use this drug?

For adults and children 2 years of age and older, apply to the affected area not more than 3 to 4 times a day. Children under 2 years of age should consult a physician.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

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

You should stop use and ask a doctor if symptoms last more than 7 days.

Is this drug safe to use during pregnancy?

There is no information regarding the safety of this drug during pregnancy.

Can nursing mothers use this drug?

There are no specific warnings or recommendations regarding the use of this product in nursing mothers.

What are the storage conditions for this drug?

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

What should I avoid while using this product?

Avoid contact with eyes. If contact occurs, rinse with water.

Are there any known drug interactions?

No specific drug interactions are mentioned in the provided text.

Is this drug for external use only?

Yes, this drug is for external use only.

Packaging Info

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

Packaging configurations for Aloe Gel Pain Reliever.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

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 properly prepared 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

For external use only. Healthcare professionals should advise patients to avoid contact with the eyes while using this product. In the event of accidental eye contact, it is imperative to rinse the eyes thoroughly with water.

Patients are also 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 Aloe Gel Pain Reliever (lidocaine hydrochloride 0.5%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aloe Gel Pain Reliever.
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 children under 2 years of age, it is advised to consult a physician prior to use.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is currently no information available regarding the use of ALOE GEL PAIN RELIEVER WELL AT WALGREENS (lidocaine hydrochloride 0.5% gel) during pregnancy. This includes any safety concerns, dosage modifications, or special precautions that may be necessary for pregnant patients. Healthcare professionals are advised to exercise caution and consider the lack of data when prescribing this product to women who are pregnant or may become pregnant. It is recommended that the potential risks and benefits be carefully weighed in the context of individual patient circumstances.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

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 available information 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 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 toxicology experts for guidance on specific management protocols and interventions that may be appropriate based on the clinical scenario.

Documentation of the incident, including the amount and timing of the substance taken, is crucial for effective management and treatment planning.

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 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 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 physician prior to 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 Aloe Gel Pain Reliever, 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 Aloe Gel Pain Reliever, 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.