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Salicylic Acid

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Active ingredient
Salicylic Acid 400 mg/1 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
January 2, 2026
Active ingredient
Salicylic Acid 400 mg/1 g
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 2025
Label revision date
January 2, 2026
Manufacturer
HY-VEE, INC
Registration number
M030
NDC root
42507-999

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Drug Overview

HyVee Medicated Maximum Strength Corn Removers are designed to help you effectively remove corns, which are thickened areas of skin that can cause discomfort. This product contains 40% salicylic acid, a medication that works by softening and dissolving the corn, making it easier to remove.

In addition to its corn removal properties, these medicated patches also cushion against pressure and friction, providing relief from pain associated with corns. With 9 pads included, you have multiple applications to help you manage and treat this common foot issue.

Uses

If you're dealing with corns, this treatment can help you by effectively removing them. Corns can be painful, and by using this product, you can find relief from that discomfort as it works to eliminate the source of your pain.

This solution is specifically designed for the removal of corns, making it a targeted option for those looking to address this common foot issue.

Dosage and Administration

To start using the medicated patch for your corn, first wash the affected area and make sure it is completely dry. If the patch is too large, you can cut it to fit the size of your corn. Once you have the right size, carefully place the medicated patch directly over the corn. To ensure it stays in place, cover the patch with a pad and press down firmly for several seconds.

You should leave the patch on for 48 hours before removing it. If the corn is still there, you can repeat this process every 48 hours as needed, but do not use it for more than 14 days. For added help in removing the corn, you may soak it in warm water for about 5 minutes before applying the patch.

What to Avoid

It's important to be cautious when considering this medication. You should not use it if you are diabetic, have poor blood circulation, or if you have irritated skin, an infection, or any reddened areas on your body. These conditions can increase the risk of complications or reduce the effectiveness of the treatment.

Additionally, be aware that this medication may be classified as a controlled substance, which means it has the potential for abuse or misuse. It's crucial to follow your healthcare provider's instructions carefully to avoid any dependence (a condition where your body becomes reliant on a substance) or other serious issues. Always prioritize your health and safety by discussing any concerns with your doctor.

Side Effects

This product is intended for external use only. You should not use it if you have diabetes, poor blood circulation, or if your skin is irritated, infected, or reddened. If you experience any discomfort that continues, it's important to stop using the product and consult a doctor.

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 for external use only. You should not use it if you are diabetic, have poor blood circulation, or if you have irritated skin or any area that is infected or reddened.

If you experience any discomfort that continues, stop using the product and consult your doctor. Additionally, if the product is swallowed, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to seek medical help immediately or contact a Poison Control Center. Signs of an overdose can vary, but they may include unusual symptoms that are not typical when taking the medication as prescribed.

Always err on the side of caution. If you suspect an overdose, don’t wait for symptoms to appear—get help right away. Your health and safety are the top priority.

Pregnancy Use

It appears that there is no specific information provided regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or any special precautions. If you are pregnant or planning to become pregnant, it is essential to consult with your healthcare provider for personalized advice and to discuss any potential risks associated with medications you may be taking. Always prioritize open communication with your doctor to ensure the best outcomes for you and your baby.

Lactation Use

If you are breastfeeding, it's important to know that the safety of this product during lactation (the period of breastfeeding) has not been established. There is a possibility that the product could be excreted in breast milk, which means it could potentially affect your baby. Therefore, you should exercise caution when considering the use of this product while nursing. Always consult with your healthcare provider to discuss any concerns and to ensure the best choices for you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If your child swallows any of it, 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 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 best performance of your product, store it in a cool, dry place at a temperature between 15° and 30°C (59° and 86°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a clean environment to avoid contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal.

Additional Information

No further information is available.

FAQ

What is HyVee Medicated Maximum Strength Corn Removers used for?

It is used for the removal of corns and relieves pain by removing them.

What is the active ingredient in HyVee Corn Removers?

The active ingredient is Salicylic Acid 40%, which is effective for corn removal.

How should I apply the medicated patch?

Wash the affected area, dry it thoroughly, cut the patch if necessary, adhere it directly over the corn, and cover it with a pad.

How long should I leave the medicated patch on?

You should leave the patch on for 48 hours, then remove it and repeat the procedure as needed for up to 14 days.

Who should not use HyVee Corn Removers?

Do not use it if you are diabetic, have poor blood circulation, or on irritated, infected, or reddened skin.

What should I do if discomfort persists?

Stop use and ask a doctor if discomfort persists.

Is this product safe for children?

Keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Can nursing mothers use this product?

The safety of this product during lactation has not been established, so caution should be exercised.

What are the storage conditions for HyVee Corn Removers?

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

Packaging Info

Below are the non-prescription pack sizes of Salicylic Acid (medicated corn 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 drug.

Uses and Indications

This drug is indicated for the removal of corns. It provides relief from pain associated with corns through its effective removal properties.

There are no teratogenic or nonteratogenic effects mentioned in the available data.

Dosage and Administration

The affected area should be washed and dried thoroughly prior to application. If necessary, the medicated patch may be cut to fit the size of the corn. The medicated patch should then be carefully adhered directly over the corn. Following application, the patch must be covered with a pad and pressed firmly for several seconds to ensure proper adhesion.

The medicated patch should be removed after 48 hours. This procedure may be repeated every 48 hours as needed, for a maximum duration of up to 14 days, or until the corn is removed. To assist in the removal of the corn, soaking the area in warm water for 5 minutes may be beneficial.

Contraindications

Use is contraindicated in patients with diabetes due to the potential for adverse effects on glycemic control. Additionally, the product should not be applied to individuals with poor blood circulation, as this may exacerbate underlying conditions. Application is also contraindicated on irritated skin or any area that is infected or reddened, as this could lead to further irritation or complications.

Warnings and Precautions

For external use only. This product is contraindicated in individuals with diabetes or those who have poor blood circulation. It should not be applied to irritated skin or any area that is infected or reddened.

Healthcare professionals should advise patients to discontinue use and consult a physician if discomfort persists.

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 should be aware that the product is for external use only. It is contraindicated in individuals who are diabetic or have poor blood circulation. Additionally, the product should not be applied to irritated skin or any area that is infected or reddened.

In the event that discomfort persists after application, patients are advised to stop use and consult a healthcare professional. It is crucial to keep the product out of reach of children. If the product is swallowed, 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 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 corn 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 medication out of 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

There is no specific information 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 should be aware that the safety of this medication during pregnancy has not been established. There are no available data regarding the potential risks or fetal outcomes associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to discuss the potential risks and benefits with their patients. It is recommended that healthcare providers exercise caution and evaluate the necessity of treatment in pregnant patients.

Lactation

The safety of this product during lactation has not been established. There is a potential for excretion in breast milk; therefore, caution should be exercised when administering this product to nursing mothers.

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 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 as necessary. It is recommended that healthcare providers follow established protocols for the management of overdosage, which may involve the administration of activated charcoal if appropriate and the implementation of other interventions based on the clinical presentation.

In all cases of suspected overdosage, the involvement of poison control and toxicology experts is advised to ensure optimal patient care and safety.

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 question. Further studies may be necessary to fully evaluate the nonclinical toxicology profile.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients that in the event of accidental ingestion, it is crucial to seek medical assistance immediately or contact a Poison Control Center. This 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 15° to 30°C (59° to 86°F) to maintain its efficacy and stability. Proper storage conditions should be observed to ensure the integrity of the product throughout its shelf life.

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.

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.