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Cvs Foot Pain

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Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
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
March 4, 2026
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Cream
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
March 4, 2026
Manufacturer
CVS Pharmacy
Registration number
M017
NDC root
51316-340
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 an external analgesic cream that provides temporary relief from pain. It contains 4% lidocaine, which works by soothing aggravated nerves, making it effective for various types of discomfort. This fast-acting cream is designed for easy application and is odor-free, making it a convenient option for those seeking relief from pain without a prescription.

In addition to its pain-relieving properties, Lidocaine also includes seven moisturizers to help care for dry skin. It is available as an over-the-counter topical analgesic, similar to other products like Aspercreme with 4% Lidocaine Foot Pain Creme, and comes in a 4-ounce bottle.

Uses

You can use this medication for the temporary relief of pain. It is designed to help alleviate discomfort, making it easier for you to go about your daily activities.

Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this medication, so it is considered safe in that regard.

Dosage and Administration

When using this medication, you should apply a thin layer to the affected area every 6 to 8 hours. However, make sure not to exceed three applications within a 24-hour period. After applying, gently massage the medication into the painful area until it is fully absorbed into your skin.

If you are considering this treatment for a child under 12 years old, it’s important to consult a doctor first to ensure it’s safe and appropriate for their use.

What to Avoid

You should avoid using this product if you have serious foot problems, such as ulcers or infections, especially on large areas of the body or on cut, irritated, or swollen skin. It is also important not to use it on puncture wounds or for more than one week without consulting your doctor.

While using this product, make sure to keep it away from your eyes and mucous membranes. Avoid tightly bandaging the area or applying local heat, like heating pads or medicated patches, and do not use it alongside other topical pain relievers. 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. Avoid using it if you have serious foot problems like ulcers or infections, on large areas of the body, or on cut, irritated, or swollen skin. It should not be applied to puncture wounds or used for more than one week without consulting a doctor.

While using this product, make sure to keep it away from your eyes and mucous membranes. Do not apply tight bandages, local heat, or use it alongside other topical pain relievers. If your condition worsens, if you notice redness or irritation, or if symptoms last more than seven days or return shortly after improvement, stop using the product and consult a doctor. Additionally, if you are pregnant or breastfeeding, it's best to ask a healthcare professional before use. If swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only. You should not use it if you have serious foot problems, such as ulcers or infections, or if you have large areas of irritated, swollen, or cut skin. Avoid using it on puncture wounds and do not use it for more than one week without consulting your doctor.

If your condition worsens, if you notice redness or irritation, or if your symptoms last longer than 7 days or return shortly after improvement, stop using the product and contact your doctor.

In case of accidental swallowing, seek emergency 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. Get medical help immediately or contact a Poison Control Center. They can provide guidance on what to do next.

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 help. Remember, it’s always better to be safe and get professional advice in these situations.

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 under 12 years old, it's important to consult with a doctor before using this medication. For children 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

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider before starting the medication. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

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 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 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 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 feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool, dry area. This helps maintain its quality over time. After each use, make sure to close the cap tightly to keep the contents secure, as the packaging is designed to be child-resistant. This precaution is important for preventing accidental access by children.

By following these simple storage and handling guidelines, you can help ensure that the product remains safe and effective for your use.

Additional Information

No further information is available.

FAQ

What is Lidocaine?

Lidocaine is an external analgesic cream that contains 4% Lidocaine and is used for the temporary relief of pain.

How should I use Lidocaine?

Apply a thin layer to the affected area every 6 to 8 hours, not exceeding 3 applications in a 24-hour period. Massage it into the skin until thoroughly absorbed.

Who should not use Lidocaine?

Do not use Lidocaine if you have serious foot problems, such as ulcers or infections, on large areas of the body, or on cut, irritated, or swollen skin.

What should I do if I experience side effects?

Stop using Lidocaine and ask a doctor if your condition worsens, if redness or irritation develops, or if symptoms persist for more than 7 days.

Is Lidocaine safe to use during pregnancy or breastfeeding?

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

What precautions should I take when using Lidocaine?

Avoid contact with eyes and mucous membranes, do not bandage tightly, and do not use at the same time as other topical analgesics.

What should I do if I swallow Lidocaine?

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

How should I store Lidocaine?

Store Lidocaine in a cool, dry area and ensure the cap is tightly closed after use.

Packaging Info

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

Packaging configurations for Cvs Foot Pain.
Details

Drug Information (PDF)

This file contains official product information for Cvs Foot Pain, 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.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

Adults and children 12 years and older are instructed to apply a thin layer of the medication to the affected area every 6 to 8 hours. The total number of applications should not exceed 3 times within a 24-hour period. It is recommended to massage the medication into the painful area until it is thoroughly absorbed into the skin.

For children under 12 years of age, it is advised to consult a doctor before use.

Contraindications

Use of this product is contraindicated in patients with serious foot problems, including ulcers or infections affecting large areas of the body, as well as on cut, irritated, or swollen skin. Application is also contraindicated on puncture wounds. Prolonged use beyond one week without consulting a healthcare professional is not recommended.

During application, contact with eyes and mucous membranes must be avoided. Additionally, tight bandaging, the application of local heat (such as heating pads), or the concurrent use of other topical analgesics is contraindicated.

Warnings and Precautions

For external use only. This product is contraindicated in patients with serious foot problems, including ulcers or infections, and should not be applied to large areas of the body, cut, irritated, or swollen skin. Additionally, it is not recommended for use on puncture wounds. Prolonged use beyond one week should only occur under the guidance of a healthcare professional.

Healthcare providers should advise patients to discontinue use and seek medical attention if any of the following occur: worsening of the condition, presence of redness, development of irritation, or if symptoms persist for more than seven days or resolve only to recur within a few days.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is contraindicated in individuals with serious foot problems, such as ulcers or infections, and should not be applied to large areas of the body, cut, irritated, or swollen skin. Additionally, the product should not be used on puncture wounds or for more than one week without consulting a healthcare professional.

During use, patients must avoid contact with the eyes and mucous membranes. It is also advised not to bandage the area tightly, apply local heat (such as heating pads), or use a medicated patch concurrently with this product.

Patients are instructed to discontinue use and seek medical advice if their condition worsens, if redness or irritation develops, or if symptoms persist for more than seven days or resolve and then recur within a few days.

Furthermore, it is recommended that individuals consult a healthcare professional before using this product if they are pregnant or breastfeeding. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

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 Foot Pain (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Foot Pain.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a healthcare professional before use. For adolescents 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

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 therapeutic response, given the lack of targeted data for 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 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 on the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating mothers.

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 drug. 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

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 understanding of the compound's potential effects in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is essential for patients to use the product only as directed and to read and follow all directions and warnings provided on the carton.

Patients should be informed to avoid contact with eyes and mucous membranes to prevent irritation or injury. Additionally, they should be cautioned against bandaging the area of use tightly or applying local heat, such as heating pads or medicated patches, as this may lead to adverse effects.

Furthermore, healthcare providers should emphasize that the product should not be used concurrently with other topical analgesics to avoid potential interactions or increased risk of side effects.

Storage and Handling

The product is supplied in child-resistant packaging, ensuring safety during storage and handling. It is essential to store the product in a cool, dry area to maintain its integrity and effectiveness. After each use, the cap should be closed tightly to prevent any contamination or degradation of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Cvs Foot Pain, 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 Foot Pain, 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.