Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Walgreens Extra Thick Callus Removers

Last content change checked dailysee data sync status

Active ingredient
Salicylic Acid 0.23 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2023
Label revision date
December 31, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Salicylic Acid 0.23 g
Other brand names
Dosage form
Patch
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 2023
Label revision date
December 31, 2025
Manufacturer
Walgreen Co.
Registration number
M030
NDC root
0363-6045
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

This medication is designed to help you remove corns and calluses, which are thickened areas of skin that can cause discomfort. By using this product, you can relieve pain associated with these skin issues. It comes with an adhesive bandage that keeps a medicated pad securely in place, ensuring effective treatment.

Uses

If you're dealing with corns and calluses, this product can help by effectively removing them. Not only does it assist in getting rid of these skin issues, but it also provides relief from the pain they can cause. The adhesive bandage included with the medicated pad ensures that it stays securely in place while you treat the affected area.

You can trust that this treatment does not have any teratogenic effects, meaning it won't cause harm to a developing fetus if used during pregnancy.

Dosage and Administration

To start treating your corn, first wash the affected area with soap and water, then dry it thoroughly. After 48 hours, you can apply a medicated bandage specifically designed for corn treatment. Once you’ve applied the bandage, remember to remove it after the same 48-hour period.

You can repeat this process every 48 hours as needed, but do not exceed 14 days of treatment. If you find it helpful, you may soak the corn in warm water for about 5 minutes before applying the bandage, as this can assist in the removal of the corn.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. If you accidentally swallow it, seek medical help immediately or contact a Poison Control Center. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence (a condition where your body becomes reliant on a substance). However, always follow the guidance provided to ensure safe use.

Side Effects

You should only use this product externally and avoid it if you have diabetes, poor blood circulation, or if your skin is irritated, infected, or reddened. If you experience discomfort that lasts, it's important to stop using the product and consult a doctor.

In case of accidental swallowing, seek medical help immediately or contact a Poison Control Center.

Warnings and Precautions

This product is intended for external use only. You should not use it if you have diabetes, poor blood circulation, or if you are applying it to irritated, infected, or reddened skin.

If you experience discomfort that lasts, stop using the product and consult your doctor. It's also 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.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to act quickly. You should seek 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 get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

When it comes to using this medication during pregnancy, specific information about its safety and any necessary dosage adjustments is not provided. Therefore, if you are pregnant or planning to become pregnant, it is essential to consult with your healthcare provider before starting this medication. They can help you understand any potential risks and make informed decisions about your treatment options. Always prioritize open communication with your doctor regarding your health and any medications you may be considering during this important time.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into your breast milk, so caution is advised. Since the effects on your nursing infant have not been thoroughly studied, be sure to keep an eye out for any unusual reactions in your baby after using the product. Your health and your baby's well-being are the top priorities, so staying informed and vigilant is key.

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 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, 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 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).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, your healthcare provider can help ensure that your treatment plan is safe and effective, taking into account all the medications and tests you may be using. Always feel free to ask questions and share your complete health history to avoid any potential issues.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place at temperatures between 0° to 40°C (32° to 104°F). This temperature range helps maintain the integrity of the device and its components.

When handling the product, always do so with clean hands and in a sterile environment to prevent contamination. If you have any specific disposal instructions, be sure to follow them carefully to ensure safe and responsible disposal.

Additional Information

You will apply the medicated bandage topically, meaning you place it directly on the skin. After 48 hours, remove the bandage and repeat the process every 48 hours as needed, up to a maximum of 14 days, or until the corn is completely removed. Make sure to follow these instructions carefully for the best results.

FAQ

What is the purpose of this drug?

This drug is used for the removal of corns and calluses and relieves pain associated with them.

How should I use this drug?

Wash the affected area and dry it thoroughly. Apply the medicated bandage after 48 hours, then remove it, and repeat every 48 hours as needed for up to 14 days.

Are there any contraindications for using this drug?

Yes, do not use this drug if you are diabetic, have poor blood circulation, or on irritated or infected skin.

What should I do if I swallow this drug?

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

Is this drug safe for use during pregnancy?

The safety of this drug during pregnancy is not specifically mentioned, so consult a healthcare professional before use.

Can nursing mothers use this drug?

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

What are the storage conditions for this drug?

Store the drug between 0° to 40°C (32° to 104°F).

What should I do if discomfort lasts after using this drug?

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

Is this drug for external use only?

Yes, this drug is for external use only.

How does the drug relieve pain?

The drug relieves pain by removing corns and calluses.

Packaging Info

Below are the non-prescription pack sizes of Walgreens Extra Thick Callus Removers (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Walgreens Extra Thick Callus Removers.
Details

Drug Information (PDF)

This file contains official product information for Walgreens Extra Thick Callus 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 specified drug.

Uses and Indications

This drug is indicated for the removal of corns and calluses. It provides relief from pain associated with these conditions by effectively removing the corns and calluses. The formulation includes an adhesive bandage that secures the medicated pad in position, ensuring optimal contact with the affected area during treatment.

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

Dosage and Administration

Healthcare professionals are advised to instruct patients to wash the affected area and dry it thoroughly before application. Following this, a medicated bandage should be applied. After 48 hours, the medicated bandage must be removed. This procedure may be repeated every 48 hours as necessary, for a maximum duration of 14 days, or until the corn is completely removed.

To facilitate the removal of the corn, patients may soak the affected area in warm water for 5 minutes prior to the application of the medicated bandage.

Contraindications

There are no contraindications listed for this product. However, it is imperative to seek medical assistance or contact a Poison Control Center immediately if the product is swallowed.

Warnings and Precautions

For external use only. This product is contraindicated in individuals with diabetes or those who exhibit 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 seek medical advice if discomfort persists. It is essential to keep this product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

Patients should be aware that the product is intended for external use only. It is contraindicated for 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 discontinue use and consult a healthcare professional.

Furthermore, if the product is ingested, it is crucial to seek medical assistance immediately or contact a Poison Control Center for guidance.

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 Walgreens Extra Thick Callus Removers (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Walgreens Extra Thick Callus 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 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 specifically established. There are no available data regarding the potential risks or fetal impacts 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 weigh the potential benefits against any unknown risks. It is recommended that pregnant patients discuss their treatment options with their healthcare provider to ensure informed decision-making regarding their health and the health of the fetus.

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 lactating mothers. The effects on the nursing infant are not well studied; it is recommended to monitor for any adverse reactions in 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 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; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. It is imperative that healthcare providers remain vigilant and prepared to address any complications that may arise from an overdosage scenario.

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.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion. It is crucial to inform patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately. This guidance is essential to ensure patient safety and prompt action in case of an emergency.

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 0° to 40°C (32° to 104°F) to maintain its efficacy and safety. Proper container requirements must be adhered to, ensuring that the product is kept in an appropriate environment. Special handling needs should be observed to prevent any compromise to the product's integrity.

Additional Clinical Information

The medication is administered topically, with a specific application protocol. Clinicians should instruct patients to apply a medicated bandage after 48 hours and to remove it subsequently. This procedure may be repeated every 48 hours as necessary, up to a maximum of 14 days, or until the corn is removed.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Walgreens Extra Thick Callus 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 Walgreens Extra Thick Callus 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

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.