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Foster and Thrive Medicated Corn Removers

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Active ingredient
Salicylic Acid 40 mg/100 mg
Other brand names
Dosage form
Plaster
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
December 5, 2025
Active ingredient
Salicylic Acid 40 mg/100 mg
Other brand names
Dosage form
Plaster
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
December 5, 2025
Manufacturer
Strategic Sourcing Services LLC
Registration number
M030
NDC root
70677-1237

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Drug Overview

Foster & Thrive Corn Remover is a product designed specifically for the removal of corns, which are thickened areas of skin that can develop on your feet. This treatment works by relieving pain associated with corns as it helps to remove them, allowing for more comfortable movement.

If you're dealing with corns, this product may provide you with the relief you need by targeting the source of discomfort and promoting healthier skin.

Uses

If you're dealing with corns, this treatment can help you by effectively removing them. Not only does it target the corns directly, but it also provides relief from the pain they cause. By using this product, you can expect to alleviate discomfort and improve your foot health.

Dosage and Administration

To start treating your corn, first wash the affected area and make sure it is completely dry. If the medicated disk is too large, you can cut it to fit the size of your corn. Once it’s the right size, apply the sticky side of the medicated disk directly onto your skin, ensuring it adheres well. After that, cover the disk with the cushion that comes with it for added protection.

You should leave the medicated disk on for 48 hours. After this time, carefully remove it. If needed, you can repeat this process every 48 hours for up to 14 days, or until the corn is completely removed. To help with the removal, you may soak the corn in warm water for about 5 minutes before applying the disk.

What to Avoid

You should avoid using this medication if you are diabetic, as it may not be safe for your condition. Additionally, if you have poor blood circulation, it’s important not to use this product, as it could worsen your situation. Never apply it to irritated skin or any area that is infected or reddened, as this could lead to further complications.

It's crucial to follow these guidelines to ensure your safety and well-being. If you have any concerns or questions about your health or the use of this medication, please consult your healthcare provider for personalized advice.

Side Effects

It's important to note that this product is for external use only. If you experience any discomfort that lasts, you should stop using the product and consult a doctor for further advice. Your health and safety are paramount, so don't hesitate to seek professional guidance if needed.

Warnings and Precautions

This product is for external use only, so please avoid swallowing it. If you accidentally swallow it, seek medical help immediately or contact a Poison Control Center at 800-222-1222.

There are no specific laboratory tests required for this product, but if you experience any discomfort that lasts, it’s important to stop using it and call your doctor for further advice. Your health and safety are the top priority, so don’t hesitate to reach out for help if needed.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect that you or someone else may have taken too much of a medication, it’s crucial to seek immediate medical help.

In case of an overdose, you should contact your local emergency services or go to the nearest hospital right away. Having the medication packaging or information on hand can help medical professionals provide the best care. Always remember that when it comes to medications, it's better to be safe and get help if you have any concerns.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no specific information available about the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions have not been clearly outlined.

Given this lack of information, you should consult with your healthcare provider before using this medication. They can help you weigh the potential risks and benefits based on your individual situation. Always prioritize open communication with your doctor regarding any medications you may be considering during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that there is no specific information available about the use of this medication during nursing. This means that the effects on breast milk and your nursing infant are not clearly defined.

As always, it's best to consult with your healthcare provider for personalized advice and to discuss any concerns you may have about medications while breastfeeding. They can help you weigh the benefits and risks based on your individual situation.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If a child swallows it, seek medical help immediately or contact a Poison Control Center at 800-222-1222. 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, 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 change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment is safe and effective, especially if you have any concerns about your kidney health. They can provide guidance based on your individual situation.

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).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

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 of your product, store it in a cool, dry place at a temperature between 20°C to 25°C (68°F to 77°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 sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

You will apply this treatment topically, meaning you will apply it directly to the skin. You can repeat the procedure every 48 hours as needed, but do not use it for more than 14 days in total, or until the corn is completely removed.

FAQ

What is Foster & Thrive Corn Remover used for?

Foster & Thrive Corn Remover is used for the removal of corns and relieves pain associated with them.

How should I apply the medicated disk?

Wash the affected area and dry it thoroughly. If necessary, cut the medicated disk to fit the corn, apply it with the sticky side adhering to the skin, and cover it with the enclosed cushion.

How often can I use the corn remover?

You can repeat the procedure every 48 hours as needed for up to 14 days until the corn is removed.

Are there any contraindications for using this product?

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

What should I do if discomfort lasts?

If discomfort lasts, stop using the product and ask a doctor for advice.

What should I do if I accidentally swallow the product?

If swallowed, get medical help or contact a Poison Control Center immediately at 800-222-1222.

Is this product safe for external use?

Yes, Foster & Thrive Corn Remover is for external use only.

What is the storage requirement for this product?

Store the product between 20°C to 25°C (68°F to 77°F).

Is there any information regarding use during pregnancy or nursing?

No specific information is provided regarding the use of this product during pregnancy or nursing.

What should I do if I have poor kidney or liver function?

There is no specific information provided regarding the use of this product for patients with kidney or liver problems.

Packaging Info

Below are the non-prescription pack sizes of Foster and Thrive Medicated Corn Removers (40% w/w salicylic acid corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Foster and Thrive Medicated Corn Removers.
Details

Drug Information (PDF)

This file contains official product information for Foster and Thrive Medicated Corn Removers, 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 action.

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 disk may be cut to fit the size of the corn. The medicated disk should be applied with the sticky side adhering to the skin, and it must be covered with the enclosed cushion.

The medicated disk should remain in place for 48 hours. After this period, the disk should be removed. This procedure may be repeated every 48 hours as needed, for a maximum duration of 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 the following situations:

Patients with diabetes should not use this product due to potential complications associated with glycemic control.

The product is contraindicated in individuals with poor blood circulation, as it may exacerbate underlying vascular issues.

Application is not recommended on irritated skin or areas that are infected or reddened, as this may lead to further irritation or infection.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to avoid ingestion of the product. In the event of accidental swallowing, immediate medical assistance is required. Patients should be instructed to contact a Poison Control Center at 800-222-1222 without delay.

It is essential to monitor patients for any signs of discomfort following use. Should discomfort persist, patients are advised to discontinue use and consult their healthcare provider for further evaluation and guidance.

Side Effects

For external use only. Patients should discontinue use and consult a doctor if discomfort persists.

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 Foster and Thrive Medicated Corn Removers (40% w/w salicylic acid corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Foster and Thrive Medicated Corn Removers.
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 Poison Control Center should be contacted at 800-222-1222.

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 they may have altered pharmacokinetics and pharmacodynamics. Close monitoring is recommended to ensure safety and efficacy in this population.

Pregnancy

There is no specific information regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in consultation with the patient. Women of childbearing potential should be advised to discuss their pregnancy status and any plans for pregnancy with their healthcare provider prior to initiating treatment.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or its effects during lactation. Healthcare professionals should consider the lack of data when advising lactating mothers about the use of this medication. It is recommended to weigh the potential benefits against any unknown risks to breastfed infants.

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 absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, increased severity of known side effects, altered mental status, or any unusual physiological responses.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. It is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for specific guidance on managing overdose cases.

In summary, while no specific overdosage information is available, healthcare professionals should exercise caution, monitor for symptoms, and provide appropriate management in the event of an overdose.

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 that in the event of accidental ingestion, it is crucial to seek medical assistance immediately. Patients should be informed to contact a Poison Control Center without delay, and the national hotline number, 800-222-1222, should be provided for their convenience. Emphasizing the importance of prompt action in such situations can help ensure patient safety and effective management of potential poisoning incidents.

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 at a controlled temperature range of 20°C to 25°C (68°F to 77°F) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept within the specified temperature limits.

Additional Clinical Information

The product is administered topically, with the procedure to be repeated every 48 hours as needed for a duration of up to 14 days, or until the corn is removed. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Foster and Thrive Medicated Corn Removers, 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 Foster and Thrive Medicated Corn Removers, 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.