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Alocane Emergency Burn

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Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2019
Label revision date
November 5, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
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 2019
Label revision date
November 5, 2024
Manufacturer
Quest Products, LLC.
Registration number
M017
NDC root
68229-201
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (12 NDCs)
Packaging & NDC Codes (12)

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

ALOCANE Burn Gel is a topical treatment designed to provide temporary relief from pain and itching caused by various skin irritations. You can use it for conditions such as sunburn, minor burns, cuts and scrapes, and insect bites. This gel comes in a convenient 2.5 fl oz tube, making it easy to apply when you need soothing relief for your skin.

Uses

If you're dealing with discomfort from sunburn, minor skin irritations, or small burns, this medication can help provide temporary relief from pain and itching. It’s also effective for soothing cuts, scrapes, and insect bites, making it a handy option for various minor skin issues.

You can use this treatment to ease the discomfort associated with these common skin problems, allowing you to feel more comfortable in your daily activities. Remember, while it can help with these specific conditions, it’s always a good idea to consult with a healthcare professional if you have any concerns.

Dosage and Administration

To use this medication effectively, start by cleaning the burn or wound area with mild soap and water. Once the area is clean, gently apply the medication directly to the affected area. You can use it up to 3 to 4 times a day, but be sure not to exceed this frequency.

If you are caring for a child under 2 years of age, it’s important to consult a doctor before using this medication. This ensures that you receive the best guidance for their specific needs.

What to Avoid

It's important to be aware of when to stop using this medication. If your condition worsens, or if your symptoms last longer than 7 days, or if they improve and then return within a few days, you should stop taking the medication and consult your doctor. This ensures that you receive the appropriate care and guidance for your health.

Currently, there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. Always prioritize your health and safety by following these guidelines.

Side Effects

You should be aware that this product is for external use only, so avoid getting it in your eyes. Keep it out of reach of children, and if it is accidentally ingested, seek medical help or contact a Poison Control Center immediately.

If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult your doctor. Additionally, if you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this product. Be cautious not to apply it in large amounts, especially on raw or blistered skin.

Warnings and Precautions

This product is for external use only, so be sure to avoid getting it in your eyes. Keep it out of reach of children, and if a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

You should stop using this product and consult your doctor if your condition worsens, if symptoms last longer than 7 days, or if they improve and then return within a few days. If you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this product. Additionally, avoid using it in large amounts, especially on raw or blistered skin.

Overdose

If you accidentally take too much of a 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 are not typical for you. If you notice anything concerning, don’t hesitate to reach out for help. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking professional advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your healthcare provider regarding your breastfeeding journey.

Pediatric Use

If your child is under 2 years old, it's important to consult a doctor before using this medication. For children aged 2 years and older, you should first clean the burn or wound area with mild soap and water. After that, you can gently apply the medication to the affected area, but be sure to limit its use to no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and promote healing.

Geriatric Use

When it comes to using ALOCANE Emergency Burn Gel, there is no specific information available about how it may affect 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 using any new medication or treatment, especially if there are existing health conditions or other medications involved. This ensures that the treatment is safe and appropriate for their individual needs.

Renal Impairment

If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help monitor your kidney function and make any necessary adjustments to your treatment plan.

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).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use with other drugs and tests. However, every individual is different, and your healthcare provider can help ensure that your treatment plan is safe and effective for you.

Always discuss any new medications or tests with your healthcare provider to avoid potential issues and to get personalized advice tailored to your health needs.

Storage and Handling

To ensure the best performance and safety of your product, store it at room temperature, ideally between 15-30°C (59-86°F). This temperature range helps maintain the integrity of the device.

When handling the product, be sure to do so in a clean environment to avoid contamination. Always follow any specific instructions provided for use and disposal to ensure safety and effectiveness.

Additional Information

You should apply the medication topically, meaning you will put it directly on the affected area of your skin. It is recommended to use it no more than 3 to 4 times a day for best results. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is ALOCANE Burn Gel used for?

ALOCANE Burn Gel is used for the temporary relief of pain and itching associated with sunburn, minor skin irritation, minor burns, cuts and scrapes, and insect bites.

How should I use ALOCANE Burn Gel?

For adults and children 2 years of age or older, clean the burn area with mild soap and water, then gently apply the gel over the burn or wound up to 3 to 4 times daily.

What should I do if I have a child under 2 years of age?

If your child is under 2 years of age, consult a doctor before using ALOCANE Burn Gel.

Are there any warnings associated with ALOCANE Burn Gel?

Yes, it is for external use only, and you should avoid contact with eyes. Keep it out of reach of children.

What should I do if I accidentally ingest ALOCANE Burn Gel?

In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

Can I use ALOCANE Burn Gel if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health care professional before using ALOCANE Burn Gel.

What should I do if my condition worsens or does not improve?

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

How should I store ALOCANE Burn Gel?

Store ALOCANE Burn Gel at room temperature between 15-30°C (59-86°F).

Packaging Info

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

Packaging configurations for Alocane Emergency Burn.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

ALOCANE Burn Gel is presented in a 2.5 fluid ounce tube. This formulation is designed for topical application to provide relief from minor burns. The product's specific composition and active ingredients are tailored to address the needs of individuals seeking effective burn care.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with sunburn, minor skin irritation, minor burns, cuts and scrapes, 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 affected burn or wound area should be cleaned with mild soap and water prior to application. The product should then be gently applied to the affected area. It is recommended that the application occurs no more than 3 to 4 times daily.

For children under 2 years of age, it is advised to consult a healthcare professional before use.

Contraindications

There are no specified contraindications for the use of this product. However, it is advised to 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.

Warnings and Precautions

For external use only; contact with the eyes should be avoided to prevent irritation or injury. It is imperative to keep this product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Healthcare professionals should advise patients to discontinue use and consult a physician if the condition worsens, if symptoms persist for more than seven days, or if symptoms resolve and then recur within a few days.

Pregnant or breastfeeding individuals are encouraged to seek guidance from a healthcare professional prior to using this product to ensure safety for both mother and child.

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

Side Effects

Patients using this product should be aware of several important warnings and precautions. This product is intended for external use only, and contact with the eyes should be avoided. In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

Patients are advised to discontinue use and consult a healthcare professional if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Additionally, pregnant or breastfeeding individuals should seek guidance from a healthcare professional prior to use.

It is important to adhere to the recommended dosage and administration guidelines. Patients should not use this product in large quantities, especially on raw surfaces or blistered areas, to minimize the risk of adverse reactions.

To ensure safety, this product should be kept out of reach of children.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

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

Packaging configurations for Alocane Emergency Burn.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a doctor prior to use. For adults and children aged 2 years and older, it is recommended to clean the burn area with mild soap and water before gently applying the product to the affected area. The product should not be used more than 3 to 4 times daily on the burn or wound.

Geriatric Use

There is no specific information regarding the use of ALOCANE Emergency Burn Gel in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when administering this product to elderly patients, as individual responses may vary. Monitoring for any adverse effects or unusual reactions is advisable, given the lack of targeted data for this population.

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. It is important to assess the potential risks and benefits, as well as any available data regarding fetal outcomes and lactation. Healthcare providers should consider individual circumstances and the specific needs of the patient when making recommendations.

Lactation

Lactating mothers are advised to consult a healthcare professional prior to using this medication. There is currently no available data regarding the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating individuals.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to 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 prescribing information.

Overdosage

In the event of accidental ingestion, it is imperative to seek immediate medical assistance or contact a Poison Control Center. Prompt action is crucial to mitigate potential risks associated with overdosage.

Healthcare professionals should be aware that symptoms of overdosage may vary depending on the substance involved. Therefore, a thorough assessment of the patient's condition is essential.

Management of overdosage typically involves supportive care and symptomatic treatment. Continuous monitoring of the patient's vital signs and clinical status is recommended. In cases where specific antidotes are available, their administration should be considered based on the clinical scenario and the substance involved.

It is essential for healthcare providers to remain vigilant and prepared to implement appropriate interventions in the event of an overdosage situation.

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 insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important for patients to understand the potential risks associated with the medication and to take necessary precautions to ensure safety.

In the event of accidental ingestion, healthcare providers should instruct patients to seek medical help immediately or contact a Poison Control Center. Emphasizing the importance of prompt action in such situations can help mitigate potential risks and ensure appropriate care.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at room temperature, maintaining a range of 15-30°C (59-86°F). Proper storage conditions are crucial to ensure the integrity and efficacy of the product.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of no more than 3 to 4 times daily on the affected area. 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 Alocane Emergency Burn, 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 Alocane Emergency Burn, 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.