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Alocane Max

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Active ingredients
  • Lidocaine Hydrochloride 4 g/100 mL
  • Benzalkonium Chloride 0.13 g/100 mL
Other brand names
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 2020
Label revision date
December 4, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Lidocaine Hydrochloride 4 g/100 mL
  • Benzalkonium Chloride 0.13 g/100 mL
Other brand names
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 2020
Label revision date
December 4, 2025
Manufacturer
Quest Products LLC
Registration number
M017
NDC root
68229-406
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (5 NDCs)
Packaging & NDC Codes (5)

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

This medication is designed to provide first aid by helping to prevent bacterial infections that can occur with skin contamination or infections. It is also effective for the temporary relief of pain and itching associated with minor conditions such as burns, cuts, sunburn, scrapes, and other minor skin irritations.

By using this product, you can help protect your skin and alleviate discomfort from these common injuries, making it a useful addition to your first aid supplies.

Uses

You can use this product for first aid to help prevent bacterial infections that may occur due to skin contamination or existing skin infections. It is also effective for providing temporary relief from pain and itching caused by minor burns, cuts, sunburn, scrapes, and other minor skin irritations.

Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this product, making it a safer option for use in various situations.

Dosage and Administration

To use this medication effectively, start by cleaning the affected area thoroughly. Once it's clean, apply a small amount of gel directly to the area that needs treatment. You can do this up to 3 to 4 times a day. If you prefer, you can cover the area with a sterile bandage, but make sure the gel has dried first.

If you are using this medication for a child under 2 years old, it's important to consult a doctor before applying it. This ensures that the treatment is safe and appropriate for their age.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should never apply it in or near your eyes, as this can cause irritation or damage. Additionally, avoid using it in large quantities or over large areas of your body, and do not apply it on raw surfaces or blistered areas, as this can lead to adverse effects.

By following these guidelines, you can help ensure that you use the medication effectively and safely. If you have any questions or concerns about its use, please consult your healthcare provider for more information.

Side Effects

It's important to be aware of some potential side effects and warnings when using this product. It is meant for external use only, so avoid applying it in or near your eyes, in large amounts, or on raw or blistered skin. If you have deep or puncture wounds, animal bites, or serious burns, consult a doctor before using it.

You should stop using the product and contact your doctor if your condition worsens, if symptoms last more than 7 days, or if they improve and then return within a few days. If you are pregnant or breastfeeding, it's best to consult a healthcare professional before use. Always keep this product out of reach of children, and if it is swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only, so please avoid using it on your eyes, in large amounts, or on raw or blistered skin. If you have deep or puncture wounds, animal bites, or serious burns, consult your doctor before using this product.

If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and contact your doctor. Additionally, keep this product out of reach of children. If it is swallowed, seek medical help or call a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to act quickly. You should seek medical help immediately or call a Poison Control Center. They can provide guidance on what to do next.

Signs of an overdose can vary, but it’s crucial to be aware of any unusual symptoms. If you notice anything concerning, don’t hesitate to reach out for help. Remember, acting fast can make a significant difference in ensuring safety and health.

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 affected area and then apply a small amount of gel. This can be done up to 3 to 4 times a day. If needed, you can cover the area with a sterile bandage, but make sure the gel has dried first. Always follow these guidelines to ensure safe and effective use for your child.

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 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 determine the best course of action based on your kidney function and overall health.

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 may affect you 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 or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any tests you might be undergoing. This way, you can avoid any potential issues and receive the best care possible.

Storage and Handling

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

When handling the product, make sure to do so in a clean environment to avoid contamination. Always follow any specific disposal instructions provided to ensure safety and compliance with local regulations.

Additional Information

No further information is available.

FAQ

What is this drug used for?

This drug is used as first aid to help prevent bacterial infection associated with contamination or skin infection, and to provide temporary relief of pain and itching from minor conditions like burns, cuts, sunburn, scrapes, and minor skin irritations.

How should I use this drug?

For adults and children 2 years and older, clean the affected area and apply a small amount of gel up to 3 to 4 times daily. It may be covered with a sterile bandage after drying.

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

If your child is under 2 years of age, you should ask a doctor before use.

Are there any warnings I should be aware of?

This drug is for external use only. Do not use it in or near the eyes, in large quantities, or on raw surfaces or blistered areas.

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.

What should I do if I accidentally swallow this drug?

Keep this drug out of reach of children. If swallowed, get medical help or call a Poison Control Center right away.

Can I use this drug if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health care professional before use.

Packaging Info

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

Packaging configurations for Alocane Max.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No description information is available for the drug.

Uses and Indications

This drug is indicated for first aid to help prevent bacterial infection associated with contamination or skin infection. It provides temporary relief of pain and itching associated with minor burns, cuts, sunburn, scrapes, and minor skin irritations.

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 area should be cleaned prior to application. A small amount of gel should be applied to the affected area no more than 3 to 4 times daily. If desired, the area may be covered with a sterile bandage, ensuring that the gel is allowed to dry before covering.

For children under 2 years of age, it is recommended to consult a physician for appropriate guidance on use.

Contraindications

Use is contraindicated in the following situations:

  • Application in or near the eyes.

  • Use in large quantities or over extensive areas of the body.

  • Application on raw surfaces or blistered areas.

These contraindications are established to prevent potential adverse effects associated with improper use.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to consult a physician prior to use if they have deep or puncture wounds, animal bites, or serious burns, as these conditions may require specialized treatment.

The product should not be applied in or near the eyes, in large quantities, or over extensive areas of the body. Additionally, it is contraindicated for use on raw surfaces or blistered areas, as these applications may lead to adverse effects.

Patients should be instructed to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

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 the local Poison Control Center should be contacted without delay.

Side Effects

Patients should be aware that the product is for external use only. It is important to consult a healthcare professional before use if there are deep or puncture wounds, animal bites, or serious burns. The product should not be applied in or near the eyes, in large quantities, or over extensive areas of the body. Additionally, it should not be used on raw surfaces or blistered areas.

Patients are advised to 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. For those who are pregnant or breastfeeding, it is recommended to seek advice from a healthcare professional prior to use.

This product should be kept out of reach of children. In the event of accidental ingestion, medical assistance should be sought immediately, or the Poison Control Center should be contacted.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Alocane Max.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a healthcare professional before use. For children aged 2 years and older, the affected area should be cleaned prior to application. A small amount of gel may be applied to the affected area no more than 3 to 4 times daily. The area may be covered with a sterile bandage after the gel has dried.

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

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, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to discuss their individual circumstances with their healthcare provider to ensure safe use during pregnancy and lactation.

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 drug insert text regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as there is no available data to guide treatment decisions in this population. Regular monitoring of renal function may be prudent in these patients, although specific recommendations are not provided.

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 an overdosage, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential.

Management procedures should include supportive care and symptomatic treatment as necessary. Continuous evaluation of the patient's condition is recommended to address any complications that may arise.

Nonclinical Toxicology

There is currently no available information regarding teratogenic effects, non-teratogenic effects, or any specific findings in the nonclinical toxicology section. Additionally, there are no details provided concerning animal pharmacology and toxicology.

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. Instruct patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use the medication in or near the eyes, in large quantities, or over large areas of the body. Additionally, it should not be applied to raw surfaces or blistered areas.

Healthcare providers should counsel patients to stop using the medication and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days.

It is also important for healthcare providers to recommend that patients ask a doctor before using the medication if they have deep or puncture wounds, animal bites, or serious burns.

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° to 30°C (59° to 86°F). Proper storage conditions are crucial to ensure the integrity and efficacy of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Alocane Max, 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 Max, 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.

Learn more in our Editorial Policy

Last AI update:

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.