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Alocane Emergency Burn Pads

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Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Swab
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2017
Label revision date
November 5, 2024
Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Swab
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2017
Label revision date
November 5, 2024
Manufacturer
Quest Products, Inc.
Registration number
M017
NDC root
68229-403

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Drug Overview

This medication is designed to provide temporary relief from pain and itching caused by various skin issues. You can use it for conditions such as sunburn, minor burns, minor skin irritation, cuts and scrapes, and insect bites. It works by soothing the affected area, helping to alleviate discomfort and promote healing.

Uses

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

This product is designed to provide quick relief, making it a handy option for treating everyday skin irritations.

Dosage and Administration

To start caring for a burn or wound, you should first clean the affected area using mild soap and water. This helps to remove any dirt or debris that could cause infection. Once the area is clean, gently apply the Alocane® Pad directly over the burn or wound.

You can use the pad on the affected area up to 3 to 4 times a day, ensuring that you follow this frequency for the best results. If you are caring for a child under 2 years of age, it’s important to consult a doctor before using this product.

What to Avoid

It's important to be aware of certain guidelines when using this medication. While there are no specific contraindications or concerns regarding abuse, misuse, or dependence, you should stop using the medication and consult your doctor if your condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then return within a few days. Always prioritize your health and safety by following these instructions closely.

Side Effects

When using this product, it's important to be aware of some potential side effects and precautions. You should only use it externally and avoid contact with 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.

Be cautious not to apply it in large amounts, especially on raw or blistered skin. 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. If you are pregnant or breastfeeding, please consult a healthcare professional before using it.

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 this medication, it’s important to seek medical help immediately or contact a Poison Control Center. Signs of an overdose can vary, but if you notice unusual symptoms, don’t hesitate to reach out for assistance.

To prevent an overdose, avoid using large amounts of the medication, especially on raw or blistered skin. Always follow the recommended dosage to ensure your safety and well-being. If you have any concerns or experience adverse effects, please consult a healthcare professional right away.

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 your 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 doctor regarding your breastfeeding journey.

Pediatric Use

When caring for burns or wounds in children aged 2 years and older, you should start by cleaning the affected area with mild soap and water. After that, gently apply the Alocane Pad over the burn or wound. It’s important to use the pad no more than 3 to 4 times a day to ensure safe and effective treatment.

If your child is under 2 years old, it’s essential to consult a doctor before using this product. This precaution helps ensure the safety and well-being of your little one.

Geriatric Use

When it comes to using Alocane Emergency Burn Pads, there is no specific information available about how they 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 using any new product, especially if there are existing health conditions or concerns. 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 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 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 helps to avoid any potential issues and ensures that you receive the best possible treatment tailored to your needs.

Storage and Handling

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

When handling the product, be sure to do so with clean hands and in a clean environment to avoid contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

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 the primary use of this drug?

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

How should I apply the drug?

Clean the burn area with mild soap and water, then gently apply the Alocane Pad over the burn or wound. Use it on the affected area no more than 3 to 4 times daily.

Are there any age restrictions for using this drug?

Children under 2 years of age should consult a doctor before use.

What should I do if my condition worsens?

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.

Is this drug safe to use during pregnancy or breastfeeding?

If you are pregnant or breastfeeding, you should ask a healthcare professional before use.

What precautions should I take when using this drug?

For external use only, avoid contact with eyes, and keep out of reach of children. In case of accidental ingestion, seek medical help immediately.

Are there any known side effects?

While specific side effects are not listed, you should stop use and consult a doctor if your condition worsens or persists.

How should I store this drug?

Store at room temperature between 15-30ºC (59-86ºF).

Packaging Info

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

Packaging configurations for Alocane Emergency Burn Pads.
Details

Drug Information (PDF)

This file contains official product information for Alocane Emergency Burn Pads, 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 and is classified as a burn pad. It is supplied in a box that contains 10 individual pads.

Uses and Indications

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

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

Dosage and Administration

The burn area should be cleaned thoroughly with mild soap and water prior to application. Following this, the Alocane® Pad should be gently applied over the affected burn or wound. The application frequency should not exceed 3 to 4 times daily.

For pediatric patients, it is advised that healthcare professionals consult a doctor before use in children under 2 years of age.

Contraindications

There are no specific contraindications listed for 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. 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 use.

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

Side Effects

Patients using this product should be aware of several important warnings and adverse reactions associated with its use. 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.

Additional precautions include keeping the product out of reach of children and avoiding the application of large quantities, especially on raw surfaces or blistered areas. 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.

For pregnant or breastfeeding individuals, it is recommended to consult a healthcare professional prior to use to ensure safety.

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 Alocane Emergency Burn Pads (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Alocane Emergency Burn Pads.
Details

Pediatric Use

Pediatric patients aged 2 years and older may use the Alocane Pad for the treatment of burns or wounds. The burn area should be cleaned with mild soap and water prior to application. The Alocane Pad should be gently applied to the affected area no more than 3 to 4 times daily.

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

Geriatric Use

There is no specific information regarding the use of Alocane Emergency Burn Pads 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 complications 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. The potential risks and benefits must be carefully considered in these populations to ensure the safety of both the mother and the fetus or infant.

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 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 this medication. Consequently, there are no 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 medical assistance immediately or contact a Poison Control Center for guidance. Prompt action is crucial to mitigate potential adverse effects associated with overdosage.

Healthcare professionals should be aware that the product should not be applied in large quantities, especially over raw surfaces or blistered areas, as this may exacerbate the risk of complications. Proper management of overdosage involves careful assessment of the patient's condition and the implementation of appropriate medical interventions as necessary.

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 15-30ºC (59-86ºF). 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 Pads, 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 Pads, 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.