ADD CONDITION

items per page

Antibacterial Lidocaine Wound Gel

Last content change checked dailysee data sync status

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)
Marketed in the U.S.
Since 2019
Label revision date
November 5, 2024
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
Marketed in the U.S.
Since 2019
Label revision date
November 5, 2024
Manufacturer
CVS Pharmacy
Registration number
M017
NDC root
69842-652

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 antibacterial gel designed to provide pain relief and help prevent infection in minor cuts, scrapes, and burns. It contains Lidocaine Hydrochloride, which is a local anesthetic that temporarily numbs the area, and Benzalkonium Chloride, which helps to keep the wound clean. This gel not only aids in pain management but also supports healing and may help reduce scarring.

As an antibiotic-free option, Lidocaine Wound Gel is a first aid treatment that you can use to care for minor injuries effectively. It is manufactured by CVS Health, ensuring a reliable choice for your wound care needs.

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’s effective in treating these minor injuries and plays a role in preventing infections that can occur in open wounds.

Additionally, this product can help reduce scarring, which is beneficial for the healing process. You can feel confident using it for your minor injuries to promote better recovery.

Dosage and Administration

To use this product effectively, start by cleaning the affected area thoroughly. For adults and children aged 2 years and older, apply a small amount of the product directly to the affected area. You can do this up to three times a day, but make sure not to exceed this limit. If the user is a child under 2 years old, it’s important to consult a doctor before using the product.

If you choose to cover the area with a sterile bandage, allow the product to dry completely first. This helps ensure that the medication works effectively while protecting the area from further irritation.

What to Avoid

It's important to use this medication safely to avoid any 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 talk to your doctor. Additionally, if the product is accidentally ingested, seek professional help or contact a Poison Control Center right away.

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 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 for further guidance.

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

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. They can provide guidance on what to do next.

Signs of an overdose can vary, but they may include unusual symptoms or changes in behavior. If you notice any concerning signs, don’t hesitate to get help. Remember, it’s always better to be safe and get professional advice in these situations.

Pregnancy Use

The safety of this product during pregnancy has not been established, which means that it may not be safe for you or your developing baby. Because of potential risks to the fetus, it is advised that you do not use this product if you are pregnant.

If you are pregnant or planning to become pregnant, it is important to consult your healthcare provider before using this product. They can help you understand the risks and make informed decisions about your health and the health of your baby.

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 not to use this product without consulting a doctor first. For children aged 2 years and older, you can apply a small amount of the product to the affected area, but be sure to do this no more than 1 to 3 times a day. Always follow these guidelines to ensure your child's safety and well-being.

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. Since older adults may have different health needs and may be taking multiple medications, it’s always a good idea to consult with a healthcare provider before starting any new medication. They can help ensure that the treatment is safe and appropriate for your individual health situation.

If you or a loved one is an older adult, be sure to discuss any concerns about potential side effects or interactions with other medications you may be taking. Your healthcare provider can provide guidance tailored to your specific 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 should be used 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).

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, 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. 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 further handling, consult 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 for first aid 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 apply a small amount of the gel on the affected area not more than 1 to 3 times daily if you are an adult or a child aged 2 years and older.

Are there any contraindications for using Lidocaine Wound Gel?

Yes, 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 the condition persists or worsens?

If the condition persists for more than 7 days or gets worse, 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, and it is advised to consult a healthcare provider before use.

Can children use Lidocaine Wound Gel?

Children under 2 years of age should not use this product without consulting a doctor.

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 if you experience any adverse reactions, stop use and consult a doctor.

How should I store Lidocaine Wound Gel?

Store Lidocaine Wound Gel at room temperature.

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 Wound Gel, developed by CVS Health, is an antibacterial gel formulated to provide pain relief while preventing infection in minor cuts, scrapes, and burns. The active ingredient, Lidocaine Hydrochloride, is complemented by Benzalkonium Chloride, enhancing its antibacterial properties. This water-based clear hydrogel is antibiotic-free and designed to help reduce scarring.

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 preventing infection and is specifically used for the treatment of minor cuts, scrapes, and burns.

Additionally, this drug helps reduce scarring associated with these minor injuries.

There are no teratogenic 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, a small amount of the product should be applied to the affected area no more than 1 to 3 times daily.

For children under 2 years of age, the product should not be used without consulting a doctor.

If desired, the treated area may be covered with a sterile bandage; however, it is important to allow the area to dry before applying the bandage.

Contraindications

Use of this product is contraindicated in the following situations:

  • Application in the eyes is prohibited due to potential for irritation or damage.

  • Application over large areas of the body, especially on raw surfaces or blistered areas, is contraindicated to prevent exacerbation of skin conditions or systemic absorption.

  • Prolonged use beyond one week is contraindicated unless directed by a healthcare professional to avoid potential adverse effects.

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 should be aware that the product is intended for external use only. It is contraindicated for application 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.

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

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 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 not use this product; consultation with a healthcare professional is advised. For adults and children aged 2 years and older, the recommended application is a small amount on the affected area, not to exceed 1 to 3 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 potential 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. Use is contraindicated in pregnancy due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a healthcare provider before using this product to discuss potential risks and benefits.

Lactation

Lactating 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. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the event of accidental ingestion, it is imperative to seek professional assistance or contact a Poison Control Center immediately. Prompt action is crucial to mitigate potential risks associated with overdosage.

Healthcare professionals should be aware that symptoms of overdosage may vary depending on the substance involved. Monitoring for any adverse effects is essential, and appropriate management should be initiated based on the clinical presentation.

Management procedures may include supportive care and symptomatic treatment, tailored to the specific symptoms exhibited by the patient. Continuous assessment and monitoring are recommended to ensure patient safety and effective intervention.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

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 of the medication. 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

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.