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Goodsense Burn Relief Gel

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 2019
Label revision date
June 28, 2019
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 2019
Label revision date
June 28, 2019
Manufacturer
Solskyn Personal Care LLC
Registration number
part348
NDC root
70281-618

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Drug Overview

GOODSENSE BURN RELIEF GEL is a topical analgesic gel that contains lidocaine HCl, which helps to soothe and relieve pain and itching. This gel is designed to provide temporary relief from discomfort associated with sunburn, minor burns, cuts, scrapes, and insect bites. Additionally, it can help alleviate itching from minor skin irritations and rashes caused by conditions like eczema and poison oak.

By restoring moisture to the skin, GOODSENSE BURN RELIEF GEL aims to enhance your comfort during recovery from these minor skin issues. Whether you're dealing with the aftermath of a sunburn or a pesky insect bite, this gel offers a supportive solution to help you feel better.

Uses

You can use this medication for temporary relief from pain and itching caused by various skin issues. This includes discomfort from sunburn, minor burns, cuts, scrapes, and insect bites. If you’re dealing with minor skin irritations or rashes, such as those from eczema, insect bites, or poison oak, this product can also help soothe the itching.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

Dosage and Administration

If you're dealing with itching from minor skin irritations or rashes caused by conditions like eczema, insect bites, or poison oak, this medication can provide you with temporary relief. It's designed specifically to help soothe that uncomfortable itching sensation.

To use the medication effectively, apply it directly to the affected area of your skin. Make sure to follow the instructions on how often to apply it, as this will help ensure you get the best results. Remember, this treatment is meant for temporary relief, so if your symptoms persist or worsen, it's important to consult a healthcare professional for further advice.

What to Avoid

It's important to use this medication responsibly. You should avoid using it in large quantities, especially on raw surfaces or blistered areas, as this can lead to complications. While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this medication, always follow the recommended guidelines to ensure your safety and well-being. If you have any questions or concerns, don't hesitate to reach out to your healthcare provider for more information.

Side Effects

This product is intended for external use only. 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 a doctor. Additionally, if your symptoms improve and then return within a few days, you should also seek medical advice.

Warnings and Precautions

This product is intended for external use only. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately. It's important to avoid using large amounts, especially on raw or blistered skin, as this can lead to complications.

While using this product, be cautious to keep it away from your eyes. If your condition worsens, if symptoms last longer than 7 days, or if symptoms improve and then return within a few days, stop using the product and consult your doctor for further advice.

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.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this product during pregnancy has not been established. You should avoid using it unless your healthcare provider specifically directs you to do so. There may be potential risks to your fetus, so consulting with a healthcare professional for personalized advice is essential.

Additionally, if you do use this product while pregnant, be aware that dosage adjustments may be necessary, and you should monitor for any adverse effects. Always prioritize open communication with your healthcare provider to ensure the best outcomes for you and your baby.

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 it may pose 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 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 GoodSense Burn Relief 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, safety concerns, or precautions outlined for elderly patients.

If you are caring for an older adult, it's always a good idea to consult with a healthcare professional before starting any new treatment. They can provide personalized advice and ensure that the product is safe and appropriate for their specific health needs.

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 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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

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 provide the best care tailored to your needs.

Always feel free to ask questions and share all the medications and supplements you are using. This helps your provider monitor your health effectively and make informed decisions about your treatment.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature, away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination and maintain its effectiveness. Once you open the container, please remember to discard it after use to avoid any potential safety issues. Following these simple guidelines will help you use the product safely and effectively.

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 your child is under 2 years old, do not use this medication without consulting a doctor first. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is GoodSense Burn Relief Gel?

GoodSense Burn Relief Gel is a topical analgesic gel that contains Lidocaine HCl, designed to soothe and relieve pain while restoring moisture.

What conditions does GoodSense Burn Relief Gel help with?

It provides temporary relief of pain and itching associated with sunburn, minor burns, cuts, scrapes, skin irritations, and insect bites.

How should I use GoodSense Burn Relief Gel?

For adults and children 2 years and older, apply to the affected area no more than 3 to 4 times daily. Do not use on children under 2 years without consulting a doctor.

Are there any contraindications for using this gel?

There are no specified contraindications, but do not use if you are pregnant unless directed by a healthcare provider.

What should I do if my symptoms persist?

Stop use and ask a doctor if your condition worsens, persists for more than 7 days, or if symptoms clear up and then recur within a few days.

Is GoodSense Burn Relief Gel safe to use during pregnancy?

The safety of this product during pregnancy has not been established, and there may be potential risks to the fetus; consult a healthcare professional for advice.

What precautions should I take when using this gel?

Use it only for external use, avoid contact with eyes, and do not apply in large quantities, especially over raw surfaces or blistered areas.

How should I store GoodSense Burn Relief Gel?

Store at room temperature, protect from light, and keep the container tightly closed. Discard after opening.

Packaging Info

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

Packaging configurations for Goodsense Burn Relief Gel.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

GOODSENSE BURN RELIEF GEL is a topical analgesic gel formulated with Lidocaine HCl. This product is designed to soothe and relieve discomfort associated with minor burns while restoring moisture to the affected area. The gel also contains Aloe, which is known for its soothing properties. The net weight of the product is 8 ounces (226 grams). This formulation can be compared to the active ingredients found in Solarcaine.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with sunburn, minor burns, minor cuts, scrapes, and minor skin irritations, including insect bites. Additionally, it provides temporary relief of itching related to minor skin irritations and rashes due to eczema, insect bites, and poison oak.

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

Dosage and Administration

For the temporary relief of itching associated with minor skin irritations and rashes due to eczema, insect bites, and poison oak, the recommended dosage is to apply a thin layer of the product to the affected area. This application should be performed up to three times daily, as needed.

Prior to application, the affected area should be cleaned and dried thoroughly. Care should be taken to avoid contact with the eyes and mucous membranes. If symptoms persist or worsen, or if there is no improvement after a specified duration, healthcare professionals should be consulted for further evaluation and management.

Contraindications

The use of this product is contraindicated in patients who may apply it in large quantities, particularly over raw surfaces or blistered areas, due to the potential for adverse effects. No other specific contraindications have been identified.

Warnings and Precautions

For external use only. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Caution is advised against the application of this product in large quantities, especially on raw surfaces or blistered areas, as this may exacerbate adverse effects.

Users should discontinue use and consult a healthcare professional if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

While using this product, it is imperative to avoid contact with the eyes to prevent irritation or injury.

Side Effects

For external use only. 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 recur within a few days.

Drug Interactions

There are no specific drug interactions reported for this medication. Additionally, no laboratory test interactions have been identified in the available data. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

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

Packaging configurations for Goodsense Burn Relief Gel.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this medication; consultation with a healthcare professional is advised. For children aged 2 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

Elderly patients may not have specific information regarding the use of GoodSense Burn Relief Gel, including dosage adjustments, safety concerns, or special precautions. As such, healthcare providers should exercise caution when considering this product for geriatric patients. Due to the lack of data, it is advisable to monitor elderly patients closely for any adverse effects or unexpected responses to treatment.

Pregnancy

The safety of this product during pregnancy has not been established. Pregnant patients should not use this product unless directed by a healthcare provider, as there may be potential risks to the fetus. It is essential for women of childbearing potential to consult a healthcare professional for advice regarding the use of this product during pregnancy.

Dosage adjustments may be necessary for pregnant individuals, and medical guidance should be sought to determine appropriate dosing. Special precautions should be taken when using this product during pregnancy, including careful monitoring for any adverse effects.

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

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 initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of specific antidotes or treatments should be considered based on the clinical scenario and the substance involved. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

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 use of the compound in question.

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 to inform patients that the product should not be used in large quantities, especially on raw surfaces or blistered areas, to prevent potential complications.

Patients should be counseled to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Additionally, healthcare providers should emphasize the importance of avoiding contact with the eyes while using this product to prevent irritation or injury.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. 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 doctor before 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 Goodsense Burn Relief 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 Goodsense Burn Relief 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.

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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.