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Salicylic Acid

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Active ingredient
Salicylic Acid 40 mg/24 1
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2012
Label revision date
January 20, 2026
Active ingredient
Salicylic Acid 40 mg/24 1
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2012
Label revision date
January 20, 2026
Manufacturer
Meijer Distribution Inc
Registration number
M028
NDC root
41250-243

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Drug Overview

Meijer Plantar Wart Remover is a topical treatment specifically designed for the removal of plantar warts, which are painful growths that appear on the bottom of the foot. This product contains salicylic acid, a medication that helps to break down the wart tissue, making it easier to remove. The remover comes in a maximum strength formula that includes 24 medicated patches and 24 concealing pads, providing a convenient way to cushion, conceal, and protect the area while effectively treating the wart.

This treatment is particularly useful for addressing the tenderness associated with plantar warts and helps restore the normal footprint pattern by targeting the wart directly. Since its introduction in January 2017, Meijer Plantar Wart Remover has been a reliable option for those seeking relief from this common foot condition.

Uses

If you have plantar warts, which are painful growths located on the bottom of your foot, this treatment can help remove them. These warts are typically identified by their specific location, tenderness, and the way they disrupt your footprint pattern.

It's important to note that this treatment does not have any known harmful effects on developing babies (teratogenic effects) or any other non-harmful effects. If you're dealing with plantar warts, this option may be suitable for you.

Dosage and Administration

To start treating your wart, first wash the affected area thoroughly. You can soak the wart in warm water for about 5 minutes to help soften it. After soaking, make sure to dry the area completely. If the medicated patches are too large, you can cut them to fit the size of your wart.

Next, apply the adhesive side of the patch directly onto the wart. To keep the patch in place and to conceal the area, cover it with pads. You should repeat this process every 48 hours as needed, continuing until the wart is removed, but no longer than 12 weeks.

What to Avoid

You should avoid using this product if you are diabetic or have poor blood circulation unless a doctor or podiatrist has advised you to do so. It's also important not to apply it to any irritated, infected, or reddened skin, as well as to avoid using it on genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them. Additionally, do not use this product on mucous membranes, as it may cause irritation or other complications. Always prioritize your health and consult a healthcare professional if you have any questions or concerns.

Side Effects

You should only use this product externally and avoid using it if you have diabetes or poor blood circulation unless your doctor or podiatrist advises otherwise. It's important not to apply it to irritated, infected, or reddened skin, as well as on genital warts, facial warts, moles, birthmarks, or warts with hair growing from them. Additionally, do not use it on mucous membranes.

Keep this product and all medications out of children's reach. If swallowed, seek medical help or contact a Poison Control Center immediately. If you experience ongoing discomfort, please consult your doctor or podiatrist.

Warnings and Precautions

This product is for external use only. You should not use it if you have diabetes or poor blood circulation unless your doctor or podiatrist has advised you to do so. Avoid applying it to irritated, infected, or reddened skin, as well as on genital warts, facial warts, moles, birthmarks, or warts with hair growing from them. It should also not be used on mucous membranes (the moist tissue lining certain body parts).

If you accidentally swallow this product, seek emergency medical help or contact a Poison Control Center immediately. Additionally, if you experience ongoing discomfort while using this product, stop using it and reach out to your doctor or podiatrist for further guidance.

Overdose

If you or someone else has swallowed too much of this 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.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to get help. Remember, acting quickly can make a significant difference in ensuring safety and health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be cautious with the use of salicylic acid. The safety of this ingredient during pregnancy has not been established, and it is generally advised against due to potential risks to the developing fetus.

Before using any products containing salicylic acid, make sure to consult your healthcare provider. They can provide guidance tailored to your specific situation and help you make informed decisions about your health and the health of your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult with your healthcare professional before using this product. There is a possibility that the product may be excreted in breast milk, which means you should be cautious when considering its use.

Additionally, the effects on your nursing infant have not been thoroughly studied, so it's essential to weigh the potential risks against the benefits. Always prioritize open communication with your healthcare provider to ensure the best choices for you and your baby.

Pediatric Use

It's important to keep this medication and all other drugs out of the reach of children to prevent accidental ingestion. If your child swallows this medication, seek medical help immediately or contact a Poison Control Center for guidance. Taking these precautions can help ensure your child's safety.

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 considering this medication, it’s important to consult with a healthcare provider. 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 change 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 situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver condition. They can help monitor your liver function and make any necessary adjustments to your treatment plan.

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 recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place where the temperature remains between 59°F and 86°F (15°C and 30°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, please refer to the guidelines provided with your product.

Additional Information

No further information is available.

FAQ

What is Meijer Plantar Wart Remover used for?

Meijer Plantar Wart Remover is used for the removal of plantar warts located on the bottom of the foot.

What active ingredient does Meijer Plantar Wart Remover contain?

It contains Salicylic Acid, which helps in the removal of warts.

How should I use Meijer Plantar Wart Remover?

Wash the affected area, soak the wart in warm water for 5 minutes, dry it thoroughly, and apply the medicated patch. Repeat every 48 hours as needed for up to 12 weeks.

Are there any contraindications for using this product?

Do not use if you are diabetic, have poor blood circulation, or on irritated, infected, or reddened skin. Avoid using on genital warts, warts on the face, moles, birthmarks, and mucous membranes.

Is Meijer Plantar Wart Remover safe to use during pregnancy?

The safety of salicylic acid during pregnancy has not been established, and it is contraindicated due to potential risks to the fetus.

What should I do if discomfort persists?

If discomfort persists, you should see your doctor or podiatrist.

How should I store Meijer Plantar Wart Remover?

Store the product between 59° and 86°F (15° and 30°C).

What should I do if the product is swallowed?

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

Can nursing mothers use Meijer Plantar Wart Remover?

Nursing mothers should consult a healthcare professional before use, as there is potential for excretion in breast milk.

Packaging Info

Below are the non-prescription pack sizes of Salicylic Acid (medicated plantar wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Salicylic Acid.
Details

Drug Information (PDF)

This file contains official product information for Salicylic Acid, 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 removal of plantar warts located on the bottom of the foot. Plantar warts are characterized by their specific location, tenderness, and disruption of the footprint pattern.

Limitations of Use: There are no known teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The affected area should be washed thoroughly, and if desired, the wart may be soaked in warm water for approximately 5 minutes to facilitate treatment. After soaking, the area must be dried completely to ensure proper adhesion of the medicated patch.

If necessary, the medicated patches can be cut to fit the size of the wart. The adhesive side of the patch should then be applied directly onto the wart. To ensure the patch remains in place and to conceal the treated area, it is recommended to cover the patch with additional pads.

This procedure should be repeated every 48 hours as needed, continuing until the wart is removed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use is contraindicated in the following situations:

Patients with diabetes or poor blood circulation should not use this product unless under the advice and supervision of a healthcare professional, due to the potential for adverse effects. Application on irritated, infected, or reddened skin is contraindicated to prevent exacerbation of these conditions. The product should not be applied to genital warts or warts located on the face, as well as to moles, birthmarks, and warts with hair growth, due to the risk of irritation or complications. Additionally, the use on mucous membranes is contraindicated to avoid potential harm.

Warnings and Precautions

For external use only. This product is contraindicated in certain populations and conditions. It should not be used by individuals who are diabetic or have poor blood circulation unless under the guidance and supervision of a qualified healthcare professional, such as a doctor or podiatrist.

Application of this product is not recommended on irritated, infected, or reddened skin. It should also be avoided on genital warts, warts located on the face, moles, birthmarks, and warts with hair growing from them. Additionally, the product must not be applied to mucous membranes.

In the event of accidental ingestion, immediate medical assistance should be sought. Contact a Poison Control Center or seek emergency medical help without delay.

Patients are advised to discontinue use and consult their doctor or podiatrist if discomfort persists. Regular monitoring and follow-up with a healthcare provider are recommended to ensure safe and effective use of this product.

Side Effects

Patients should be aware that the product is for external use only. It is contraindicated in individuals who are diabetic or have poor blood circulation, unless used under the advice and supervision of a doctor or podiatrist. The product should not be applied to irritated, infected, or reddened skin, nor should it be used on genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them. Additionally, it should not be applied to mucous membranes.

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

If discomfort persists after application, patients are advised to consult their doctor or podiatrist for further evaluation and management.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 Salicylic Acid (medicated plantar wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Salicylic Acid.
Details

Pediatric Use

Pediatric patients should be advised to keep this and all medications out of the reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

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 potential adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

The safety of salicylic acid during pregnancy has not been established. Salicylic acid is contraindicated in pregnancy due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a healthcare provider before using this medication to discuss potential risks and benefits.

Lactation

Nursing mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk; therefore, caution is advised when administering to nursing mothers. The effects on the nursing infant are not well studied; thus, the risks versus benefits should be considered.

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 are no established 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 available 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 assessment of potential risks associated with the use of the compound in these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this medication and all other drugs out of the reach of children to prevent accidental ingestion. It is crucial to emphasize the importance of safety in the home environment, particularly for households with young children.

In the event that the medication is swallowed, healthcare providers should instruct patients to seek medical help immediately or contact a Poison Control Center. Prompt action is essential to ensure the safety and well-being of the patient.

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 within a temperature range of 59° to 86°F (15° to 30°C) to maintain its efficacy and integrity. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable environment to prevent degradation.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Salicylic Acid, 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 Salicylic Acid, 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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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.