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Antibacterial Lidocaine Wound Gel

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Active ingredients
  • Lidocaine Hydrochloride 2 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 2019
Label revision date
November 5, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Lidocaine Hydrochloride 2 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 2019
Label revision date
November 5, 2024
Manufacturer
ASO LLC
Registration number
M017
NDC root
51142-652
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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Drug Overview

Lidocaine Wound Gel is a water-based clear hydrogel designed to help prevent infection in minor cuts, scrapes, and burns. It contains Lidocaine Hydrochloride (a local anesthetic that temporarily relieves pain) and Benzalkonium Chloride (an antibacterial agent), making it effective for treating these minor injuries while also helping to reduce scarring.

This gel is antibiotic-free and serves as a first aid option to provide both protection and pain relief for minor burns and skin injuries. If you have a small cut or scrape, Lidocaine Wound Gel can be a supportive choice to aid in your healing process.

Uses

You can use this product for first aid to help prevent infection in minor cuts, scrapes, and burns. It’s designed to protect these injuries and keep them clean. Additionally, it provides temporary relief from pain associated with minor burns, helping you feel more comfortable as you heal.

Dosage and Administration

To use this medication effectively, start by cleaning the affected area thoroughly. If you are an adult or a child aged 2 years and older, you can apply the medication to the affected area up to 3 to 4 times a day. For children under 2 years of age, it’s important to consult a doctor before use.

If you choose to cover the area with a sterile bandage, make sure to let the medication dry completely first. This will help ensure that the treatment works effectively while protecting the area from further irritation.

What to Avoid

You should avoid using this medication in your eyes or applying it over large areas of your body, especially on raw or blistered skin. It's important to follow these guidelines to prevent potential harm. Additionally, do not use this medication for more than a week unless your doctor specifically instructs you to do so. Always prioritize your safety and consult with a healthcare professional if you have any questions or concerns.

Side Effects

You should be aware that this product is for external use only and should not be applied to your eyes or over large areas of your body, especially on raw or blistered skin. It's important not to use it for longer than a week unless your doctor advises you to do so. If you have deep or puncture wounds, animal bites, or serious burns, consult your doctor before using this product.

If your condition does not improve after 7 days, worsens, or clears up only to return within a few days, stop using the product and seek medical advice. Additionally, if the product is accidentally ingested, contact a Poison Control Center or seek professional help immediately.

Warnings and Precautions

This product is for external use only, so please avoid applying it to your eyes or on large areas of your body, especially over raw or blistered skin. You should not use it for more than a week unless your doctor advises otherwise.

Before using this product, consult your doctor if you have deep or puncture wounds, animal bites, or serious burns. If your condition does not improve after 7 days, worsens, or clears up only to return within a few days, stop using the product and contact your doctor.

Keep this product out of reach of children. If a child accidentally ingests it, seek professional help or contact a Poison Control Center right away.

Overdose

If you or someone else accidentally takes too much of a medication, it's important to act quickly. You should seek professional assistance or contact a Poison Control Center right away. Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing (respiratory depression).

If you notice any of these symptoms, do not hesitate to get help. Remember, it's always better to be safe and get professional advice in these situations.

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 consult your doctor before using it, as there may be potential risks to your fetus that are not clearly defined.

While there are no specific dosage modifications recommended for pregnant individuals, it's always best to seek guidance from a healthcare professional to ensure your safety and that of your baby. Caution is advised, so please prioritize open communication with your doctor regarding any medications you may consider.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your doctor before using this product. There is a possibility that it may be excreted in breast milk, which means it could potentially affect your baby. Since the effects on nursing infants have not been thoroughly studied, it's best to exercise caution. Always prioritize your health and your baby's well-being by discussing any concerns with your healthcare provider.

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 can apply it to the affected area, but be sure not to exceed 3 to 4 applications in a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about how it may affect you or if any dosage adjustments are necessary. This means that the usual guidelines for safety and precautions that apply to elderly patients have not been established.

If you are an older adult or a caregiver, it's important to consult with a healthcare professional before starting this medication. They can provide personalized advice and ensure that it is safe and appropriate for your individual health 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 may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

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 remember that discussing your full list of medications and any lab tests with your healthcare provider is crucial. This way, you can avoid any potential issues and receive the best care tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. This means keeping it in a place that is neither too hot nor too cold, typically between 68°F and 77°F (20°C to 25°C).

When handling the product, make sure to do so with clean hands or gloves to maintain its safety and effectiveness. Always follow any specific instructions provided with the product for proper use and disposal.

Additional Information

No further information is available.

FAQ

What is Lidocaine Wound Gel used for?

Lidocaine Wound Gel is an antibacterial gel that helps prevent infection and is used for treating minor cuts, scrapes, and burns. It also helps reduce scarring.

How should I apply Lidocaine Wound Gel?

Clean the affected area and apply the gel not more than 3 to 4 times daily for adults and children 2 years of age and older. Consult a doctor for children under 2 years.

Are there any contraindications for using this gel?

Do not use Lidocaine Wound Gel in the eyes, over large areas of the body, or longer than a week unless directed by a doctor.

What should I do if my condition does not improve?

Stop using the gel and ask a doctor if the condition persists for more than 7 days or worsens.

Is it safe to use Lidocaine Wound Gel during pregnancy?

The safety of Lidocaine Wound Gel during pregnancy has not been established, so consult a doctor if you are pregnant or planning to become pregnant.

Can nursing mothers use this product?

Nursing mothers should consult a doctor before using Lidocaine Wound Gel, as there is a potential for excretion in breast milk.

What should I do in case of accidental ingestion?

In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

What are the side effects of Lidocaine Wound Gel?

For external use only, and you should stop use and consult a doctor if the condition worsens or does not improve within 7 days.

Packaging Info

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

Packaging configurations for Antibacterial Lidocaine Wound Gel.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Lidocaine Hydrochloride 2% is a topical formulation designed for the management of minor cuts, scrapes, and burns. This product contains Benzalkonium Chloride at a concentration of 0.13%, serving as a preservative. The formulation is presented as a water-based clear hydrogel, which facilitates easy application and absorption.

This antibacterial gel is specifically designed to help prevent infection in minor wounds while also aiding in the reduction of scarring. The absence of antibiotics in the formulation ensures a focus on antibacterial properties without the use of antimicrobial agents.

Uses and Indications

This drug is indicated for first aid to help prevent infection in minor cuts, scrapes, and burns. Additionally, it provides temporary relief of pain associated with minor burns.

Limitations of Use: This drug is not intended for use on deep wounds, animal bites, or serious burns.

Dosage and Administration

The affected area should be cleaned prior to application. For adults and children aged 2 years and older, the product should be 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.

If desired, the treated area may be covered with a sterile bandage. In such cases, it is important to allow the area to dry completely before applying the bandage.

Contraindications

Use of this product is contraindicated in the following situations:

The product should not be applied to the eyes due to the potential for irritation or damage to ocular tissues. Additionally, it is contraindicated for use over large areas of the body, especially on raw surfaces or blistered areas, as this may increase the risk of systemic absorption and adverse effects. Prolonged use beyond one week is also contraindicated unless specifically directed by a healthcare professional, to prevent potential complications associated with extended exposure.

Warnings and Precautions

For external use only. This product is contraindicated for application in the eyes and should not be used over large areas of the body, particularly on raw surfaces or blistered areas. Prolonged use beyond one week is not recommended unless directed by a healthcare professional.

Healthcare providers should advise patients to consult a doctor prior to use if they have deep or puncture wounds, animal bites, or serious burns.

Patients are instructed to discontinue use and seek medical advice if the condition does not improve after 7 days, worsens, or if the condition resolves and then recurs within a few days.

It is imperative to keep this product out of reach of children. In the event of accidental ingestion, immediate professional assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

Patients using this product should be aware of several important warnings and precautions. This product is intended for external use only and should not be applied in or around the eyes. It is contraindicated for use over large areas of the body, especially on raw surfaces or blistered areas. Additionally, the product should not be used for longer than one week unless directed by a healthcare professional.

Before using this product, patients should consult a doctor if they have deep or puncture wounds, animal bites, or serious burns.

Patients are advised to discontinue use and seek medical advice if the condition persists for more than seven days, worsens, or if the condition resolves and then recurs within a few days.

In the event of accidental ingestion, it is crucial to seek professional assistance or contact a Poison Control Center immediately.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions with 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 Antibacterial Lidocaine Wound Gel (benzalkonium chloride, lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Antibacterial Lidocaine Wound Gel.
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 recommended application is to the affected area not more than 3 to 4 times daily.

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

The safety of this product during pregnancy has not been established. Pregnant patients or those planning to become pregnant should consult a healthcare professional before use. While potential risks to the fetus are not clearly defined, caution is advised when considering the use of this product in this population. There are no specific dosage modifications for pregnant individuals; therefore, healthcare professionals should provide guidance based on individual circumstances.

Lactation

Nursing mothers should consult a doctor before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are not well studied; therefore, caution is advised.

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.

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 event of accidental ingestion, it is imperative to seek professional assistance without delay. Healthcare professionals should contact a Poison Control Center immediately for guidance on managing the situation effectively.

Prompt intervention is crucial in mitigating potential risks associated with overdosage. The specific symptoms of overdosage may vary depending on the substance involved; therefore, a thorough assessment and appropriate management strategies should be employed based on the clinical presentation and guidance from poison control experts.

Healthcare providers are advised to monitor the patient closely for any adverse effects and to initiate supportive care as necessary. This may include symptomatic treatment and stabilization of vital signs. It is essential to document the incident and any interventions performed for future reference and to inform ongoing patient 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 professional assistance or contact a Poison Control Center immediately in the event of accidental ingestion. It is important for patients to understand the potential risks associated with unintentional consumption and to act swiftly to ensure their safety.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers assigned for identification. It is essential to store the product at room temperature to maintain its integrity and efficacy. No special handling requirements are noted; however, standard precautions should be observed to ensure optimal storage conditions.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Antibacterial Lidocaine Wound 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 Antibacterial Lidocaine Wound 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.

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.