Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Lidocaine Pain Relief with Lavender

Last content change checked dailysee data sync status

Active ingredient
Lidocaine Hydrochloride 38 mg/1 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2021
Label revision date
October 3, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 38 mg/1 mL
Other brand names
Dosage form
Liquid
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 2021
Label revision date
October 3, 2024
Manufacturer
Natural Essentials, Inc.
Registration number
M017
NDC root
66902-057
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 is a topical pain relief medication that comes in a convenient roll-on form, designed to provide temporary relief from pain. It contains a 4% concentration of lidocaine hydrochloride, which helps numb areas affected by pain without causing irritation. This product is formulated to be non-greasy and easy to apply, making it a practical choice for those seeking quick and effective pain relief.

In addition to its pain-numbing properties, Lidocaine also includes lavender essential oil, which adds a calming aromatherapy effect. This combination not only targets pain but also promotes a soothing experience, similar to other products containing lidocaine, such as Aspercreme.

Uses

You can use this medication for the temporary relief of pain. It works by helping to numb the areas affected by pain, providing you with comfort without causing irritation. This can be particularly helpful when you're dealing with discomfort and need a quick solution to ease your symptoms.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you should apply a thin layer of the medication to the affected area every 6 to 8 hours. However, make sure not to apply it more than three times in a 24-hour period. This helps ensure that you are using the medication safely and effectively.

For children under 12 years of age, it’s important to consult a doctor before using this medication. They can provide guidance on the appropriate treatment for younger patients. Always follow your healthcare provider's instructions to achieve the best results.

What to Avoid

You should avoid using this product on large areas of your body, on cut, irritated, or swollen skin, and on puncture wounds. It's important not to use it for more than one week without consulting your doctor. While using the product, make sure to keep it away from your eyes, and do not bandage the area or apply local heat, such as heating pads.

If you notice that your condition worsens, experience skin reactions like rash, itching, redness, irritation, pain, swelling, or blistering, or if your symptoms persist for more than seven days, stop using the product and consult your doctor. Additionally, if your symptoms clear up and then return within a few days, seek medical advice. Remember, this product is flammable, so keep it away from fire or flames.

Side Effects

If you experience any worsening of your condition, skin reactions like rash, itching, redness, irritation, pain, swelling, or blistering, or if your symptoms persist for more than 7 days, you should stop using the product and consult a doctor. Additionally, if your symptoms improve and then return within a few days, seek medical advice.

This product is for external use only and is flammable, so keep it away from fire or flames. Avoid using it on large areas of the body, on cuts, irritated, or swollen skin, and do not apply it to puncture wounds. If you accidentally swallow the product, seek medical help or contact a Poison Control Center immediately. Always follow the directions on the packaging and avoid contact with your eyes.

Warnings and Precautions

This product is for external use only, so please avoid applying it to large areas of your body or on any cut, irritated, or swollen skin. It should not be used on puncture wounds, and you should not use it for more than one week without consulting your doctor. Always follow the directions on the packaging carefully, and be sure to keep it away from your eyes. Avoid using bandages or applying heat, like heating pads, to the area where you apply the product.

If you notice that your condition worsens, or if you experience any skin reactions such as rash, itching, redness, irritation, pain, swelling, or blistering, stop using the product and contact your doctor. Additionally, if your symptoms last longer than seven days or clear up only to return within a few days, seek medical advice. Remember, this product is flammable, so keep it away from fire or flames. Always store it out of reach of children and pets, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, it’s important to act quickly. Contact a medical professional or call a Poison Control Center immediately for guidance.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, seek immediate medical attention. Remember, it’s always better to be safe and get help if you think an overdose has occurred.

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 expert 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 doctor regarding your breastfeeding journey.

Pediatric Use

If your child is 12 years old or younger, it's important to consult with a doctor before using this medication. For children aged 12 and older, you can apply a thin layer of the product to the affected area every 6 to 8 hours, but be sure not to exceed three applications in a 24-hour period. Always follow these guidelines to ensure safe and effective use for your child.

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 course of action 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.

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 should be used if you have hepatic impairment (liver issues).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

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 may not have known conflicts with other drugs or tests. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective based on your unique health situation.

Always discuss any changes in your medication or health status with your healthcare provider to avoid potential issues and to get the best care possible.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place away from direct sunlight. Excessive moisture can damage the product, so it's important to keep it protected from humidity. Always make sure the lid is closed tightly when not in use to maintain its integrity.

By following these simple storage guidelines, you can help ensure that your product remains effective and safe for use. If you have any questions about handling or storage, feel free to reach out for more information.

Additional Information

No further information is available.

FAQ

What is Lidocaine used for?

Lidocaine is used for the temporary relief of pain and helps numb pain-affected areas without irritation.

How should I apply Lidocaine?

For adults and children 12 years and older, apply a thin layer to the affected area every 6 to 8 hours, not exceeding 3 applications in a 24-hour period.

Can children use Lidocaine?

Children 12 years or younger should ask a doctor before use.

Are there any warnings for using Lidocaine?

Yes, do not use Lidocaine on large areas of the body, on cut or irritated skin, or for more than one week without consulting a doctor.

What should I do if I experience side effects?

Stop using Lidocaine and ask a doctor if conditions worsen, skin reactions occur, or symptoms persist for more than 7 days.

Is Lidocaine flammable?

Yes, Lidocaine is flammable, so keep it away from fire or flame.

What should I do if Lidocaine is swallowed?

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

Can I use Lidocaine while pregnant or breastfeeding?

If pregnant or breastfeeding, ask a health professional before use.

How should I store Lidocaine?

Store Lidocaine with the lid closed tightly, away from direct sunlight and excessive moisture.

Packaging Info

Below are the non-prescription pack sizes of Lidocaine Pain Relief with Lavender (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Lidocaine Pain Relief with Lavender.
Details

Drug Information (PDF)

This file contains official product information for Lidocaine Pain Relief with Lavender, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Lidocaine HCl 4% is a topical anesthetic formulation designed for the temporary relief of pain. This product contains lavender essential oil, which contributes to its calming properties through aromatherapy. The formulation is characterized by a non-greasy, no-mess consistency, allowing for easy application to pain-affected areas without causing irritation. The actual bottle size is 2.5 fluid ounces (73 mL).

Uses and Indications

This drug is indicated for the temporary relief of pain. It provides effective numbing of pain-affected areas without causing irritation.

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

Dosage and Administration

For adults and children aged 12 years and over, a thin layer of the medication should be applied to the affected area every 6 to 8 hours. The total number of applications must not exceed 3 times within a 24-hour period.

For children under 12 years of age, it is recommended to consult a physician for appropriate dosing and administration guidance.

Contraindications

Use of this product is contraindicated in the following situations:

Application on large areas of the body or on cut, irritated, or swollen skin is prohibited due to the potential for exacerbating these conditions. The product should not be applied to puncture wounds, as this may lead to complications. Prolonged use beyond one week without consulting a healthcare professional is also contraindicated to prevent adverse effects.

During use, contact with the eyes must be avoided to prevent irritation or injury. Additionally, bandaging or applying local heat, such as heating pads, to the area of application is not recommended, as this may alter the product's efficacy and safety profile.

Patients should discontinue use and consult a physician if any of the following occur: worsening of conditions, skin reactions such as rash, itching, redness, irritation, pain, swelling, or blistering, persistence of symptoms beyond seven days, or recurrence of symptoms after initial resolution within a few days.

Due to its flammable nature, the product must be kept away from fire or flame to prevent fire hazards.

Warnings and Precautions

For external use only. This product should not be applied to large areas of the body, nor should it be used on cut, irritated, or swollen skin. It is contraindicated for application on puncture wounds and should not be used for more than one week without consulting a healthcare professional.

When utilizing this product, it is imperative to adhere strictly to the provided directions. Users must read and follow all instructions and warnings indicated on the carton. Care should be taken to avoid contact with the eyes. Additionally, the area of application should not be bandaged or subjected to local heat, such as heating pads.

Discontinue use and seek medical advice if any of the following occur: worsening of conditions, skin reactions including rash, itching, redness, irritation, pain, swelling, or blistering. If symptoms persist beyond seven days or if they resolve and then recur within a few days, medical consultation is advised. This product is flammable; therefore, it must be kept away from fire or flame.

It is essential to keep this product out of reach of children and pets. In the event of ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center should be made without delay.

Side Effects

Patients using this product may experience a range of adverse reactions. Serious reactions warrant immediate medical attention, particularly if conditions worsen or if skin reactions occur. Such skin reactions may include rash, itching, redness, irritation, pain, swelling, and blistering. Patients should discontinue use and consult a healthcare professional if symptoms persist for more than 7 days or if symptoms resolve and then recur within a few days.

It is important to note that this product is for external use only and is flammable; therefore, it should be kept away from fire or flame. Patients are advised against using the product on large areas of the body, on cut, irritated, or swollen skin, or on puncture wounds. Additionally, the product should not be used for more than one week without consulting a doctor.

While using this product, patients should adhere strictly to the directions provided on the carton. Care should be taken to avoid contact with the eyes, and patients should refrain from bandaging or applying local heat, such as heating pads, to the area of use.

In the event of accidental ingestion, patients should seek medical help 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 between the drug and 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 Lidocaine Pain Relief with Lavender (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Lidocaine Pain Relief with Lavender.
Details

Pediatric Use

Pediatric patients 12 years of age and younger should consult a healthcare professional before use. For patients aged 12 years and older, the recommended dosage is to apply a thin layer to the affected area every 6 to 8 hours, with a maximum of 3 applications within a 24-hour period.

Geriatric Use

There is no specific information available regarding the use of this medication 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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

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 considered in these populations to ensure the safety of both the mother and the fetus or infant.

Lactation

Lactating mothers are advised to consult a health 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

Patients with renal impairment have not been specifically addressed in the drug insert regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of detailed guidance 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 relation to this medication. Consequently, there are no 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 an overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous monitoring and evaluation are recommended to ensure patient safety and effective resolution of any complications arising from the overdosage.

Nonclinical Toxicology

If pregnant or breastfeeding, it is advised to consult a health professional prior to use. No specific non-teratogenic effects have been identified. Additionally, there are no detailed findings related to nonclinical toxicology or animal pharmacology and toxicology available.

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 and pets to prevent accidental ingestion. Instruct patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately.

It is essential for patients to use the medication only as directed. They should be encouraged to read and follow all directions and warnings provided on the carton to ensure safe and effective use.

Healthcare providers should also inform patients to avoid contact with the eyes, as this could lead to irritation or injury. Additionally, patients should be cautioned against bandaging or applying local heat, such as heating pads, to the area of use, as this may exacerbate potential side effects or interfere with the medication's effectiveness.

Storage and Handling

The product is supplied in a configuration that ensures optimal preservation of its integrity. It is essential to store the product in a cool, dry place, away from direct sunlight, to maintain its efficacy. The container must be kept tightly closed to prevent contamination and preserve the product's quality. Additionally, it is crucial to protect the product from excessive moisture, which could compromise its stability. Proper handling and storage conditions are vital for ensuring the product remains effective throughout its intended shelf life.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Lidocaine Pain Relief with Lavender, 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 Lidocaine Pain Relief with Lavender, 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.