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2.0% Lidocaine Burn

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Active ingredient
Lidocaine Hydrochloride 2 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2026
Label revision date
February 5, 2026
Active ingredient
Lidocaine Hydrochloride 2 g/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2026
Label revision date
February 5, 2026
Manufacturer
Nantong Health & Beyond Hygienic Products Inc.
Registration number
M017
NDC root
43473-097

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

2.0% Lidocaine Burn is a topical medication designed to provide temporary pain relief for minor burns. It works by numbing the affected area, helping to alleviate discomfort and promote a sense of relief. If you are dealing with a minor burn, this product may help ease your pain and support your healing process.

Uses

If you’re dealing with minor burns, this medication can provide you with temporary pain relief. It’s designed to help ease the discomfort that comes from these types of injuries, allowing you to feel more comfortable as you heal.

Rest assured, this medication does not have any known teratogenic effects, meaning it does not cause harm to a developing fetus. This makes it a safer option for those who are pregnant or may become pregnant.

Dosage and Administration

To use the burn spray effectively, start by cleaning the affected area thoroughly. Once it's clean, spray an even layer of the burn spray over the area. You can do this up to 3 to 4 times a day, but make sure not to exceed this limit for the best results.

It's important to note that this burn spray is not recommended for children under 12 years of age, so please keep that in mind when considering its use. Always follow these guidelines to ensure safe and effective treatment.

What to Avoid

It's important to keep this medication out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately. There are no specific contraindications, risks of abuse or misuse, or concerns about dependence associated with this medication, so you can feel assured about its use in the appropriate context. Always follow the guidance provided by your healthcare professional.

Side Effects

This product is for external use only, so please avoid using it in large amounts, especially on raw or blistered skin, and keep it away from your eyes. If the product accidentally gets into your eyes, rinse them thoroughly with water. You should stop using the product and consult a doctor if your condition worsens, lasts more than 7 days, or improves and then returns.

It's important to keep this product out of reach of children. 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 in large amounts, especially on raw or blistered skin. Be careful not to apply it near your eyes; if it does come into contact with your eyes, rinse them thoroughly with water. If your condition worsens, lasts more than 7 days, or improves and then comes back, stop using the product and consult your doctor.

Keep this product out of reach of children. If it is swallowed, seek medical help immediately or contact a Poison Control Center. Your safety is important, so please take these precautions seriously.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, it’s important to act quickly. You should seek medical help immediately or contact a Poison Control Center for guidance.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. Always err on the side of caution and reach out for professional help if you have any concerns about an overdose. Your safety is the top priority.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be cautious with any medications, including 2.0% Lidocaine Burn Spray. Currently, there is no specific information available about its safety, dosage adjustments, or any special precautions for use during pregnancy. This means that the potential risks and benefits of using this spray while pregnant are not clearly defined.

Before using this product, you should consult with your healthcare provider to discuss your individual situation and any concerns you may have. They can help you make informed decisions about your care during pregnancy.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or considerations 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 it may pose to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

It's important to know that this medication should not be used in children under 12 years of age. If you have younger children, make sure to keep the medication out of their reach to prevent accidental ingestion. In the event that a child swallows the medication, seek medical help or contact a Poison Control Center immediately. Your child's safety is a top priority, so always follow these guidelines carefully.

Geriatric Use

When considering medication for older adults, it's important to note that this particular drug is not recommended for children under 12 years of age. If you are caring for an older adult, ensure that any medications prescribed are appropriate for their age and health status. Always consult with a healthcare provider to discuss any specific concerns or questions regarding medication use in older individuals.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for your condition in the provided information. This means that the standard recommendations for medication use may apply to you without any special considerations. However, always consult your healthcare provider for personalized advice and to ensure your treatment is safe and effective based on your kidney health.

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 for the medication do not change based on liver function. However, it’s always a good idea to discuss your liver health with your healthcare provider before starting any new medication. They can help ensure that your treatment is safe and effective for you.

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 health concerns to receive the best care possible.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place at a temperature between 68°F and 77°F (20°C to 25°C). This temperature range helps maintain the integrity of the device.

When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage. Always keep it 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

You should apply the burn spray topically, which means you will spray an even layer over the cleaned affected area. It is recommended to do this no more than 3 to 4 times a day for best results. There are no additional details regarding laboratory tests, abuse potential, or patient counseling information available at this time.

FAQ

What is 2.0% Lidocaine Burn used for?

2.0% Lidocaine Burn is used for temporary pain relief associated with minor burns.

How should I use 2.0% Lidocaine Burn?

You should spray an even layer of the burn spray over the cleaned affected area no more than 3-4 times daily.

Is 2.0% Lidocaine Burn safe for children?

No, it should not be used on children under 12 years of age.

What should I do if I swallow 2.0% Lidocaine Burn?

If swallowed, you should get medical help or contact a Poison Control Center right away.

Are there any warnings associated with 2.0% Lidocaine Burn?

Yes, it is for external use only, should not be used in large quantities, particularly over raw or blistered areas, and should not be used near the eyes.

What should I do if my condition worsens or does not improve?

You should stop using the product and ask a doctor if the condition worsens or persists for more than 7 days.

Is there any information about using 2.0% Lidocaine Burn during pregnancy?

No specific information regarding pregnancy use or safety concerns is provided for 2.0% Lidocaine Burn.

Can nursing mothers use 2.0% Lidocaine Burn?

There are no specific warnings or considerations mentioned regarding the use of this product by nursing mothers.

What is the recommended storage temperature for 2.0% Lidocaine Burn?

You should store it at 68°-77°F (20°-25°C).

Packaging Info

Below are the non-prescription pack sizes of 2.0% Lidocaine Burn (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for 2.0% Lidocaine Burn.
Details

Drug Information (PDF)

This file contains official product information for 2.0% Lidocaine Burn, 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 specified drug.

Uses and Indications

This drug is indicated for the temporary relief of pain associated with minor burns.

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

Dosage and Administration

Healthcare professionals are advised to apply an even layer of the burn spray to the cleaned affected area. This application should not exceed 3 to 4 times daily.

It is important to note that this product is contraindicated for use in children under 12 years of age.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical assistance should be sought or contact with a Poison Control Center is advised.

Warnings and Precautions

For external use only. It is imperative that this product not be applied in large quantities, particularly over raw or blistered areas. Care should be taken to avoid contact with the eyes; in the event of accidental exposure, the eyes should be rinsed thoroughly with water.

Healthcare professionals should advise patients to discontinue use and seek medical advice if the condition worsens or persists for more than 7 days, or if the condition appears to improve and then returns.

General precautions must be observed, including keeping the product out of reach of children. In the event of ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

In cases of accidental swallowing, it is crucial to obtain emergency medical help or contact a Poison Control Center without delay.

Side Effects

Patients should be aware that the product is for external use only. It is contraindicated for use in large quantities, particularly over raw or blistered areas, and should not be applied near the eyes. In the event of contact with the eyes, it is advised to rinse thoroughly with water.

Patients are instructed to discontinue use and consult a healthcare professional if the condition worsens or persists for more than 7 days, or if the condition clears up and then returns.

Additionally, it is crucial to keep the product out of reach of children. In the case of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Drug Interactions

There are currently no documented drug interactions associated with 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 2.0% Lidocaine Burn (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for 2.0% Lidocaine Burn.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this medication. It is essential to keep the product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Geriatric Use

Elderly patients should be considered when prescribing this medication, particularly those aged 65 years and older. It is important to note that this medication is not indicated for use in children under 12 years of age.

Healthcare providers should exercise caution when prescribing to geriatric patients, as age-related physiological changes may affect drug metabolism and response. Monitoring for efficacy and safety is recommended, and dose adjustments may be necessary based on individual patient factors.

Clinical findings specific to the geriatric population should be taken into account to ensure optimal therapeutic outcomes while minimizing potential risks.

Pregnancy

There is no specific information regarding the use of 2.0% Lidocaine Burn Spray in pregnant patients, including safety concerns, dosage modifications, or special precautions during pregnancy. Healthcare professionals should consider the lack of data when prescribing this medication to women of childbearing potential. Given the absence of established risk categories or known fetal impacts, the potential benefits and risks should be carefully weighed in the context of individual patient circumstances.

Lactation

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

Renal Impairment

There is no information available regarding renal impairment, including dosage adjustments, special monitoring, or safety considerations for patients with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of specific guidance when treating patients with renal impairment.

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 caution and consider the lack of data when prescribing this medication to patients with liver problems.

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 of the patient's condition is essential.

Management procedures should include supportive care and symptomatic treatment as necessary. Continuous monitoring of the patient's vital signs and clinical status is recommended to ensure appropriate interventions are implemented in a timely manner.

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 compound in these areas.

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. In the event that the medication is swallowed, patients should be instructed to seek medical help immediately or contact a Poison Control Center for assistance. It is important for patients to understand the urgency of this situation to ensure their safety and the safety of others.

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 a controlled temperature range of 68° to 77°F (20° to 25°C) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept within this temperature range at all times.

Additional Clinical Information

The product is administered topically, with the recommended direction to spray an even layer of burn spray over the cleaned affected area no more than 3-4 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 2.0% Lidocaine Burn, 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 2.0% Lidocaine Burn, 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.