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Cvs Pain Relief Roll-on Lidocaine with Lavender

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Active ingredient
Lidocaine Hydrochloride 40 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Lotion
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2026
Label revision date
February 12, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 40 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Lotion
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 2026
Label revision date
February 12, 2026
Manufacturer
CVS Pharmacy
Registration number
M017
NDC root
51316-273
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 Pain Relief Roll-On is a topical product that contains 4% lidocaine HCL (a local anesthetic that helps numb pain) and lavender essential oil. This non-greasy, no-mess formula is designed to provide temporary relief from pain by numbing the affected areas without causing irritation.

In addition to its pain-relieving properties, the roll-on includes calming lavender aromatherapy, making it a soothing option for those seeking relief. It is available without a prescription and is comparable to other products containing lidocaine, such as Aspercreme.

Uses

You can use this medication for the temporary relief of pain. It works by numbing the areas affected by pain, providing you with comfort without causing irritation. This can be particularly helpful when you need quick relief from discomfort.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those concerned about such risks.

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 exceed three applications within a 24-hour period. This means you can use it multiple times a day, but keep track to avoid overuse.

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 these instructions carefully to ensure safe and effective use.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should not apply it to large areas of your body or on any cut, irritated, or swollen skin. Additionally, avoid using it on puncture wounds. If you find that you need to use this medication for more than one week, please consult your doctor for guidance. Following these instructions will help ensure your safety and the effectiveness of the treatment.

Side Effects

When using this product, it's important to apply it only as directed and avoid using it on large areas of your body, on broken or irritated skin, or for more than one week without consulting a doctor. Be cautious to keep it away from your eyes and do not apply heat or bandage the treated area.

You should stop using the product and consult a doctor if you experience worsening conditions or any skin reactions, such as rash, itching, redness, irritation, pain, swelling, or blistering. If your symptoms last longer than seven days or clear up only to return shortly after, seek medical advice. Additionally, if you are pregnant or breastfeeding, it's best to consult a healthcare professional before use. If the product is swallowed, seek medical help immediately or contact a Poison Control Center.

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. If you are pregnant or breastfeeding, consult a healthcare professional before using this product. Keep 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. They can provide you with the necessary steps to take based on the specific situation.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to seek immediate medical attention. Your safety is the top priority, so getting help quickly can make a significant difference.

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 those aged 12 and older, you can apply a thin layer 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 always a good idea to discuss any medications with a healthcare provider. They can help determine the best approach, considering any unique health needs or conditions.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will guide you on the appropriate use of this medication based on individual health status. Always keep them informed about any other medications being taken or any health changes that occur.

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 may affect you 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 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 conditions you have to receive the best care possible.

Storage and Handling

To ensure the best performance and safety of your product, it's important to store it properly. Keep the product away from direct sunlight, as exposure can affect its quality. Additionally, protect it from excessive moisture, which can also compromise its effectiveness. Always make sure the lid is closed tightly when not in use to maintain its integrity.

When handling the product, be mindful of these storage conditions to ensure it remains in optimal condition. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is Lidocaine Pain Relief Roll-On used for?

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

How should I apply Lidocaine Pain Relief Roll-On?

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 Pain Relief Roll-On?

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

Are there any warnings for using this product?

Yes, it is for external use only. Do not use 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 skin reactions?

Stop use and ask a doctor if conditions worsen or if skin reactions such as rash, itching, or blistering occur.

Is it safe to use Lidocaine Pain Relief Roll-On if I am pregnant or breastfeeding?

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

What should I do if I accidentally swallow the product?

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

What are the ingredients in Lidocaine Pain Relief Roll-On?

It contains Lidocaine HCL 4% and Lavender Essential Oil, providing a non-greasy, no-mess formula.

How should I store Lidocaine Pain Relief Roll-On?

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

Packaging Info

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

Packaging configurations for Cvs Pain Relief Roll-on Lidocaine with Lavender.
Details

Drug Information (PDF)

This file contains official product information for Cvs Pain Relief Roll-on Lidocaine with Lavender, 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. It is designed to help numb areas affected by pain 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 advised to consult a physician before use.

Contraindications

Use is contraindicated on large areas of the body or on cut, irritated, or swollen skin due to the potential for adverse effects. Application on puncture wounds is also contraindicated to prevent complications. Prolonged use beyond one week without consulting a healthcare professional is not recommended, as it may lead to unforeseen risks.

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.

Users are advised to discontinue use and consult a physician 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 symptoms resolve and then recur within a few days, medical advice should be sought.

For individuals who are pregnant or breastfeeding, it is recommended to consult a healthcare professional prior to use.

This product should be kept out of reach of children and pets. In the event of accidental 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 should be aware that it is intended for external use only. It is contraindicated for application on large areas of the body, on cut, irritated, or swollen skin, and on puncture wounds. Additionally, the product should not be used for more than one week without consulting a healthcare professional.

During use, patients must adhere strictly to the directions provided and avoid contact with the eyes. Bandaging or applying local heat, such as heating pads, to the area of application is not recommended.

Patients are advised to discontinue use and seek medical advice 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 if symptoms resolve and then recur within a few days.

Furthermore, it is important for patients who are pregnant or breastfeeding to consult a healthcare professional prior to use. In the event 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 Cvs Pain Relief Roll-on Lidocaine with Lavender (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Pain Relief Roll-on Lidocaine with Lavender.
Details

Pediatric Use

Pediatric patients 12 years of age and younger should consult a healthcare professional prior to 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

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 weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is no specific data available regarding the excretion of this medication in 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 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 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 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 and monitoring of the patient are essential.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous evaluation and appropriate interventions should be implemented based on the clinical presentation and severity of symptoms.

In all cases of suspected overdosage, the involvement of poison control experts is recommended to guide the management process effectively.

Nonclinical Toxicology

If pregnant or breast-feeding, it is advised to consult a health professional prior to use. No non-teratogenic effects have been specified in the available data. Additionally, there are no details provided regarding nonclinical toxicology or animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the product out of reach of children and pets to prevent accidental ingestion or exposure. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use the product on large areas of the body or on cut, irritated, or swollen skin, and it should not be applied to puncture wounds. It is important to counsel patients against using the product for more than one week without consulting a doctor.

Patients should be instructed to stop using the product and seek medical advice if their condition worsens or if they experience any skin reactions, such as rash, itching, redness, irritation, pain, swelling, or blistering. Additionally, they should be advised to discontinue use and consult a doctor if symptoms persist for more than seven days or if symptoms clear up and then recur within a few days.

When using the product, patients must be reminded to follow all directions and warnings on the carton carefully. They should be cautioned against allowing the product to come into contact with their eyes and advised not to bandage or apply local heat, such as heating pads, to the area of use.

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 prevent degradation. Additionally, the product must be protected from excessive moisture, which could compromise its quality. To maintain its efficacy, the lid should be closed tightly when not in use. Proper adherence to these storage conditions is crucial 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 Cvs Pain Relief Roll-on Lidocaine 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 Cvs Pain Relief Roll-on Lidocaine 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.

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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.