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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 2022
Label revision date
October 14, 2025
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 2022
Label revision date
October 14, 2025
Manufacturer
WALGREENS
Registration number
M017
NDC root
0363-1652
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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

Lidocaine Wound Gel is a clear, water-based gel that serves as an external analgesic, meaning it helps relieve pain. It contains Lidocaine Hydrochloride (2%), which provides temporary relief from pain associated with minor cuts, scrapes, and burns. Additionally, it includes Benzalkonium Chloride (0.13%), which acts as a first aid antiseptic to help prevent infection and reduce scarring.

This gel is designed to be gentle on the skin, as it is fragrance-free, hypoallergenic, and paraben-free, making it suitable for those with sensitive skin. You can use Lidocaine Wound Gel to soothe minor injuries while also protecting them from potential infections.

Uses

You can use this product for first aid to help prevent infection and to temporarily relieve pain from minor cuts, scrapes, and burns. It is effective in treating these minor injuries and can also help reduce scarring while preventing infection.

Feel confident knowing that there are no teratogenic effects (harmful effects on fetal development) associated with this product, making it a safe option for use in various situations.

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 the medication has dried completely first. This will help ensure that the treatment works effectively while protecting the area from further irritation.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should never apply it to your eyes or over large areas of your body, especially on raw or blistered skin. Additionally, do not use it for more than a week unless your doctor specifically instructs you to do so. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

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 more 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 if it clears up and then comes back within a few days, stop using the product and seek medical advice. Always keep this product out of reach of children, and if it 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 large areas of your body, especially on raw or blistered skin. You should not use it for more than a week unless your doctor advises you to do so.

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 accidentally take too much of a medication, it's important to act quickly. You should seek professional assistance or contact a Poison Control Center right away. They can provide you with the guidance you need.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for you. If you notice any concerning changes in your health after taking a medication, don’t hesitate to reach out for help. Remember, it’s always better to be safe and get the support you need.

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 provided for pregnant individuals, it’s always best to seek guidance from a healthcare professional regarding any medications you may consider. Taking these precautions can help ensure the health and safety of both you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

When using this medication for children aged 2 years and older, you can apply it to the affected area up to 3 to 4 times a day. However, if your child is under 2 years old, it's important to consult a doctor before use. This ensures that the treatment is safe and appropriate for their age. Always follow these guidelines to help keep your child safe and healthy.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s wise to discuss any potential risks or benefits with your healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so regular check-ins with your doctor can ensure safety and effectiveness. If you notice any unusual side effects or changes in health, be sure to report these to your healthcare team promptly.

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 your kidneys are not functioning properly.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your kidney health. They can help monitor your condition 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 (issues with liver function).

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 you understand how to manage your treatment effectively.

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 share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. This helps maintain its effectiveness and safety. When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage. Always keep the product in a clean environment to ensure it remains safe for use. If you have any questions about disposal or other safety measures, please refer to the guidelines provided with your product.

Additional Information

No further information is available.

FAQ

What is Lidocaine Wound Gel used for?

Lidocaine Wound Gel is used as a first aid treatment to help prevent infection and provide temporary relief of pain associated with minor cuts, scrapes, and burns.

How should I apply Lidocaine Wound Gel?

You should 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. For children under 2 years, consult a doctor.

Are there any contraindications for using Lidocaine Wound Gel?

You should 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?

If your condition persists for more than 7 days or worsens, you should stop using the gel and consult a doctor.

Is Lidocaine Wound Gel safe to use 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.

What precautions should I take when using Lidocaine Wound Gel?

Keep Lidocaine Wound Gel out of reach of children, and in case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

What are the key ingredients in Lidocaine Wound Gel?

Lidocaine Wound Gel contains Lidocaine Hydrochloride 2% and Benzalkonium Chloride 0.13%, making it an external analgesic and first aid antiseptic.

Can I cover the area after applying Lidocaine Wound Gel?

Yes, you may cover the area with a sterile bandage after applying the gel, but let it dry first.

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

No description information is available.

Uses and Indications

This drug is indicated for first aid to help prevent infection and for the temporary relief of pain associated with minor cuts, scrapes, and burns. It is effective in treating minor cuts, scrapes, and burns, and it aids in reducing scarring while helping to prevent infection.

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

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

The product is contraindicated for use in the eyes. Additionally, it should not be applied over large areas of the body, especially on raw surfaces or blistered areas, due to the potential for adverse effects. Prolonged use beyond one week is contraindicated unless directed by a healthcare professional to mitigate risks associated with extended application.

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 within 7 days or if it worsens. Additionally, if the condition resolves and then recurs within a few days, medical consultation is warranted.

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 should be aware that the product is for external use only. It is contraindicated for use in the eyes, over large areas of the body, particularly on raw surfaces or blistered areas, and should not be used for longer than one week unless directed by a healthcare professional.

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

Patients should discontinue use and seek medical advice if the condition persists for more than seven days, worsens, or if the condition clears up and recurs within a few days.

Additionally, this product should be kept out of reach of children. In the event of accidental ingestion, it is crucial to seek professional assistance or contact a Poison Control Center immediately.

Drug Interactions

There are currently no documented drug interactions associated with the use of this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

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 aged 2 years and older may apply the medication 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 prior to use.

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 efficacy, 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 pregnant individuals. There are no specific dosage modifications for pregnant patients; therefore, it is essential to seek guidance from a healthcare professional regarding appropriate use during pregnancy.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

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 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 professional assistance without delay. Healthcare professionals should contact a Poison Control Center immediately to obtain guidance on the appropriate management of the situation.

Symptoms of overdosage may vary depending on the substance involved and the amount ingested. It is crucial for healthcare providers to monitor the patient closely for any signs of toxicity and to initiate supportive care as necessary.

Management procedures should include a thorough assessment of the patient's condition, including vital signs and any presenting symptoms. Depending on the severity of the overdosage, further interventions may be required, such as activated charcoal administration or other specific treatments as recommended by the Poison Control Center.

Prompt action and adherence to established protocols are essential in mitigating the effects of overdosage and ensuring patient safety.

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 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 available 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

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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.