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Alocane Plus

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Active ingredients
  • Lidocaine Hydrochloride 4 g/100 mL
  • Benzalkonium Chloride 0.13 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 2013
Label revision date
July 17, 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
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 2013
Label revision date
July 17, 2025
Manufacturer
Quest Products, Inc.
Registration number
M017
NDC root
68229-300
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (3 NDCs)
Packaging & NDC Codes (3)

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 temporary relief from pain and itching caused by various skin issues, including sunburn, minor cuts and scrapes, minor skin irritation, and minor burns. It can help soothe discomfort and promote a sense of relief when you experience these common skin conditions.

While the specific mechanism of action isn't detailed, you can trust that this product is formulated to address your immediate needs for comfort and care in managing minor skin irritations.

Uses

If you're dealing with discomfort from sunburn, minor cuts and scrapes, minor skin irritation, or minor burns, this medication can help provide temporary relief from pain and itching. It's designed to soothe your skin and alleviate those bothersome symptoms, allowing you to feel more comfortable.

Rest assured, there are no concerns regarding teratogenic effects (which means it doesn't cause birth defects) associated with this medication. You can use it with confidence for the indicated purposes.

Dosage and Administration

When using this medication, you should apply it to the affected area no more than 3 to 4 times a day. It's important to avoid using large amounts, especially on raw surfaces or blistered areas, as this can lead to irritation or other issues.

If you are considering this treatment for a child under 2 years old, be sure to consult a physician (a medical doctor) first to ensure it's safe and appropriate for their use. Always follow these guidelines to help ensure effective and safe treatment.

What to Avoid

It's important to be mindful of your health when using this medication. If your condition worsens, or if your symptoms last longer than 7 days or improve and then return within a few days, you should stop using the medication and consult your doctor. This ensures that you receive the appropriate care and guidance for your health needs. Always prioritize your well-being and seek professional advice when necessary.

Side Effects

It's important to use this product only on the skin and avoid getting it in your eyes. If your condition worsens, or if your symptoms last longer than 7 days or come back after clearing up, you should stop using the product and consult your doctor.

If you are pregnant or breastfeeding, please talk to a healthcare professional before using this product to ensure it is safe for you.

Warnings and Precautions

This product is for external use only, so be sure to avoid getting it in your eyes. It's important to keep it out of reach of children to prevent any accidental use.

If you notice that your condition worsens, or if your symptoms last longer than 7 days, or if they improve and then come back within a few days, stop using the product and consult your doctor. Additionally, if you are pregnant or breastfeeding, please talk to a healthcare professional before using this product to ensure it is safe for you.

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 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 you have a child under 2 years old, it's important to consult a physician (doctor) before using this medication. This ensures that the treatment is safe and appropriate for your child's specific needs. Always prioritize professional guidance when it comes to the health of young children.

Geriatric Use

While there is no specific information about the use of ALOCANE PLUS in older adults, it's important to approach any new medication with caution. Since the drug insert does not mention dosage adjustments or safety concerns for elderly patients, you should consult with a healthcare professional before starting this medication. They can help determine if ALOCANE PLUS is appropriate for you or your loved one, considering any unique health needs or conditions. Always prioritize open communication with your doctor about any medications you are taking, especially if you are an older adult or caring for one.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no dosage adjustments, special monitoring, or safety considerations to discuss for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to consult your healthcare provider for personalized advice and guidance.

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.

However, it's always best to discuss your individual health situation with your healthcare provider, as they can offer personalized advice and ensure that any medications you take are safe for your liver health.

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. This helps to create a comprehensive picture of your health and ensures your safety while receiving treatment.

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 product's effectiveness and safety.

When handling the product, make sure to do so in a clean environment to avoid contamination. Always follow any specific instructions provided with the product for safe use and disposal. Keeping these guidelines in mind will help you use the product safely and effectively.

Additional Information

You should apply the medication to the affected area no more than 3 to 4 times a day. This helps ensure that you are using it safely and effectively. If you have any questions about how to use the medication or its effects, be sure to consult with your healthcare provider.

FAQ

What is this drug used for?

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

How often can I apply this drug?

You can apply it to the affected area not more than 3 to 4 times daily.

Are there any contraindications for this drug?

No specific contraindications are mentioned for this drug.

What should I do if my condition worsens?

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

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

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

Is this drug safe for children?

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

What precautions should I take while using this drug?

For external use only, avoid contact with eyes, and keep out of reach of children.

What is the storage condition for this drug?

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

Packaging Info

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

Packaging configurations for Alocane Plus.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is a topical gel with an SPL Code of 34089-3. It contains 0.5% lidocaine as the active ingredient. The gel is clear and colorless in appearance. Inactive ingredients include aloe vera gel, carbomer, glycerin, propylene glycol, purified water, sodium hydroxide, and triethanolamine.

Uses and Indications

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

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

Dosage and Administration

The medication should be applied to the affected area no more than 3 to 4 times daily. It is important to avoid the use of large quantities, especially over raw surfaces or blistered areas, to prevent potential adverse effects. For children under 2 years of age, consultation with a physician is recommended prior to use.

Contraindications

There are no specific contraindications identified 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 strictly avoided to prevent irritation or injury. It is imperative to keep this product out of reach of children to prevent accidental ingestion or misuse.

Healthcare professionals should advise patients to discontinue use and consult a physician if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

In cases of pregnancy or breastfeeding, it is essential for individuals to seek guidance from a healthcare professional prior to using this product to ensure safety for both the mother and child.

Side Effects

Patients should be aware that the product is for external use only and should avoid contact with the eyes. In the event that the condition worsens, or if symptoms persist for more than 7 days or clear up and then occur again within a few days, patients are advised to stop use and consult a healthcare professional.

Additionally, it is recommended that individuals who are pregnant or breastfeeding seek guidance from a healthcare professional prior to using this product.

Drug Interactions

There are no specific drug interactions or laboratory test interactions identified in the available data. Therefore, no dosage adjustments or monitoring recommendations are necessary at this time.

Packaging & NDC

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

Packaging configurations for Alocane Plus.
Details

Pediatric Use

Pediatric patients under 2 years of age should be evaluated by a physician prior to use. It is important to consider the specific needs and potential risks associated with this age group when determining treatment options.

Geriatric Use

There is no specific information regarding the use of ALOCANE PLUS in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication 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. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice 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

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 information available 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 clinical judgment when considering the use of this medication in patients with liver problems, as the absence of specific guidance necessitates careful evaluation of the potential risks and benefits.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks associated with overdosage.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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.

Patients should be instructed to stop using the medication and consult their 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. This guidance is essential to ensure appropriate management of their condition and to avoid potential complications.

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

Patients should apply the medication to the affected area no more than 3 to 4 times daily. 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 Plus, 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 Plus, 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.