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Menthol

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Active ingredient
Menthol 10 mg/1 g
Other brand names
Dosage form
Powder
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
May 27, 2025
Active ingredient
Menthol 10 mg/1 g
Other brand names
Dosage form
Powder
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2025
Label revision date
May 27, 2025
Manufacturer
Target Corporation
Registration number
M017
NDC root
82442-211

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Drug Overview

Medicated Foot Powder is a topical product designed to provide temporary relief from pain and itching caused by minor skin irritations. It features a triple-action formula that absorbs moisture, alleviates itching, and helps control foot odor, making it a helpful option for maintaining foot comfort.

The powder contains menthol (1%), which acts as an external analgesic, providing a soothing effect. This product is talc-free and is comparable to the active ingredient found in Gold Bond, ensuring you can find relief without the use of talc.

Uses

If you're dealing with minor skin irritations, this medication can help provide temporary relief from pain and itching. It's designed specifically for these types of discomfort, allowing you to feel more comfortable in your daily activities.

Rest assured, there are no concerns regarding teratogenic effects (which means it doesn't cause birth defects) associated with this medication. This makes it a safer option for those who may be pregnant or planning to become pregnant.

Dosage and Administration

To use this medication effectively, start by washing and drying your feet thoroughly. Once your feet are clean, sprinkle the powder generously on the affected areas, including between your toes and on the bottoms of your feet.

If you are an adult or a child aged 2 years and older, you can apply this powder up to 3 to 4 times a day. However, if your child is under 2 years old, it’s important not to use this product without first consulting a doctor. Following these steps will help ensure you get the best results from the treatment.

What to Avoid

You should avoid contact with your eyes when using this product. If your condition worsens, or if your symptoms persist for more than 7 days or improve and then return within a few days, stop using the product and consult a doctor. It's important to follow these guidelines to ensure your safety and well-being.

Side Effects

When using this product, it's important to avoid contact with your eyes. If you notice that your condition worsens, or if your symptoms last longer than 7 days or improve only to return shortly after, you should stop using the product and consult a doctor.

Additionally, 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 intended for external use only, so please avoid applying it near your eyes. If you notice that your condition worsens while using this product, or if your symptoms last longer than 7 days or return shortly after improving, stop using it and consult your doctor.

It's important to keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately. Your safety is a priority, so please take these precautions seriously.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

There is currently no specific information available regarding the use of Menthol maximum strength medicated foot powder during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before using any medication, including over-the-counter products like this foot powder. They can provide personalized advice based on your health needs.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that the drug insert for Menthol maximum strength medicated foot powder does not provide specific information about its use during nursing. This means there are no established guidelines or known effects on breast milk or your nursing infant.

As always, it's a good idea to consult with your healthcare provider before using any medication while breastfeeding to ensure the safety and well-being of both you and your baby.

Pediatric Use

If your child is under 2 years old, it's important not to use this medication without consulting a doctor first. For children aged 2 years and older, you can apply the medication to the affected area, but make sure to do so no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

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 information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to be adjusted based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific condition. They can help monitor your kidney health and make any necessary changes to your medications.

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 provided 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. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, always ensure that your healthcare provider is aware of all the medications you are using, as this helps them provide the best care tailored to your needs.

By discussing your full medical history and any other treatments, you can help prevent potential issues and ensure your safety.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place. It's important to keep the container tightly closed to prevent contamination and protect it from excessive heat, which can affect its quality. Avoid freezing the product, as this can cause damage. Once you open the container, be sure to discard any unused product to maintain safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is Medicated Foot Powder used for?

Medicated Foot Powder is used for the temporary relief of pain and itching associated with minor skin irritations.

How does Medicated Foot Powder work?

It features a triple-action formula that absorbs moisture, relieves itching, and helps control foot odor, with menthol as an external analgesic.

Who can use Medicated Foot Powder?

Adults and children 2 years of age and older can use it, while children under 2 years should consult a doctor.

How should I apply Medicated Foot Powder?

You should wash and dry your feet thoroughly, then sprinkle the powder liberally on your feet, between your toes, and on the bottoms of your feet, applying it not more than 3 to 4 times daily.

Are there any warnings for using Medicated Foot Powder?

Yes, it is for external use only, and you should avoid contact with the eyes. Stop use and consult a doctor if conditions worsen or symptoms persist for more than 7 days.

What should I do if I accidentally swallow Medicated Foot Powder?

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

How should I store Medicated Foot Powder?

Store it in a cool, dry place, keep the container tightly closed, protect it from excessive heat, and do not freeze.

Are there any known side effects of Medicated Foot Powder?

The provided information does not list specific side effects, but you should stop use and consult a doctor if you experience worsening conditions or persistent symptoms.

Packaging Info

Below are the non-prescription pack sizes of Menthol (maximum strength medicated foot powder talc free). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Menthol.
Details

Drug Information (PDF)

This file contains official product information for Menthol, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Medicated Foot Powder is a maximum strength formulation designed for external use. It contains 1% menthol, which serves as an external analgesic. This triple-action formula effectively absorbs moisture, alleviates itching, and aids in controlling foot odor. The product is talc-free and is packaged in a net weight of 10 ounces (283 grams).

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor skin irritations.

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

Dosage and Administration

Adults and children aged 2 years and older are instructed to apply the product to the affected area no more than 3 to 4 times daily. For children under 2 years of age, the product should not be used without consulting a doctor.

Prior to application, it is essential to wash and dry the feet thoroughly. The powder should be sprinkled liberally on the feet, ensuring coverage between the toes and on the bottoms of the feet.

Contraindications

There are no specific contraindications listed for this product. However, it is advised to avoid contact with the eyes. If conditions worsen, or if symptoms persist for more than 7 days or resolve and then recur within a few days, discontinue use and consult a healthcare professional.

Warnings and Precautions

This product is intended for external use only. Healthcare professionals should advise patients to avoid contact with the eyes during application. In the event that the condition worsens, or if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days, patients should be instructed to discontinue use and consult a physician.

It is imperative to keep this product out of reach of children. In cases of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

Patients using this product should be aware that it is intended for external use only. Care should be taken to avoid contact with the eyes, as this may lead to adverse effects.

In clinical practice, patients are advised to discontinue use and consult a healthcare professional if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

Additionally, it is crucial to keep this product out of reach of children. In the event of accidental ingestion, patients should seek medical assistance or contact a Poison Control Center immediately.

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Menthol (maximum strength medicated foot powder talc free). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Menthol.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this medication; consultation with a healthcare professional is advised. For children aged 2 years and older, the recommended application is to the affected area no more than 3 to 4 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 adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is no specific information regarding the use of Menthol maximum strength medicated foot powder during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when recommending this product to women of childbearing potential and consider the lack of data on potential fetal impacts. It is advisable to weigh the benefits against any unknown risks when considering the use of this product in pregnant patients.

Lactation

There is no specific information regarding the use of Menthol maximum strength medicated foot powder in lactating mothers or any lactation considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution and consider the lack of data when advising lactating mothers on the use of this product. The potential effects on breastfed infants have not been established.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of this medication. Consequently, there is no information available 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.

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 may vary depending on the specific substance involved, and monitoring for any adverse effects is essential.

Management of overdosage should include supportive care and symptomatic treatment as necessary. Continuous assessment of the patient's condition is recommended to address any complications that may arise.

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 seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important to emphasize the necessity of avoiding contact with the eyes to prevent potential irritation or injury.

Patients should be instructed to discontinue use and consult a doctor if their condition worsens. Additionally, they should be informed to stop using the product and seek medical advice if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. This guidance is crucial for ensuring patient safety and effective management of their condition.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored in a cool, dry place, away from excessive heat. Freezing is not permitted, as it may compromise the product's quality. After opening, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Menthol, 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 Menthol, 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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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.