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Salicylic Acid

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Active ingredient
Salicylic Acid 0.17 g/1 g
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2008
Label revision date
October 8, 2025
Active ingredient
Salicylic Acid 0.17 g/1 g
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2008
Label revision date
October 8, 2025
Manufacturer
Walgreen Company
Registration number
M030
NDC root
0363-9889

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Drug Overview

Liquid Corn & Callus Remover is a topical treatment that contains 17% salicylic acid, a medication that helps to remove corns and calluses from the skin. This product works by softening and breaking down the thickened skin, which not only helps to eliminate these growths but also provides relief from the pain they can cause.

In addition to its primary function, Liquid Corn & Callus Remover includes cushioning to protect your skin from friction caused by shoes, making it a supportive option for those dealing with discomfort from corns and calluses.

Uses

If you're dealing with corns and calluses, this treatment can help you by effectively removing them. By getting rid of these thickened areas of skin, you can also find relief from the pain they may be causing. This means you can enjoy more comfort in your daily activities without the discomfort that corns and calluses can bring.

Dosage and Administration

To start treating your corn or callus, first wash the affected area with soap and water, then dry it thoroughly. Using the provided applicator, apply one drop of the medication at a time directly onto the corn or callus, ensuring that it is completely covered. Allow the area to dry after each application.

For added comfort, you can use cushions that have a hole in the center, which will help relieve pressure on the corn or callus. These cushions can be purchased separately if needed. You should repeat this application process once or twice daily, as necessary, for up to 14 days, or until the corn or callus is completely removed.

What to Avoid

It's important to be cautious when using this medication. You should not apply it to any irritated skin or areas that are infected or reddened. If you have diabetes or poor blood circulation, you should also avoid using this product, as it may not be safe for you.

Additionally, be aware that misuse or abuse of this medication can lead to dependence (a condition where your body becomes reliant on a substance). Always follow these guidelines to ensure your safety and well-being.

Side Effects

When using this product, it's important to be aware of certain warnings and precautions. This product is for external use only and should not be applied to irritated, infected, or reddened skin. If you have diabetes or poor blood circulation, you should avoid using it. If you experience any discomfort that persists, please consult your doctor or podiatrist.

Additionally, take care to avoid contact with your eyes and do not inhale the vapors. If the product accidentally gets into your eyes, rinse them with water for 15 minutes. Always keep this product out of reach of children, and if it is swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only and should be kept away from fire or flames, as it is flammable. Make sure to cap the bottle tightly and store it at room temperature, away from heat sources.

Do not use this product on irritated skin, infected areas, or if you have diabetes or poor blood circulation. While using it, avoid contact with your eyes and do not inhale the vapors. If you accidentally get the product in your eyes, rinse them with water for 15 minutes. If you experience ongoing discomfort, please consult your doctor or podiatrist.

Keep this product out of reach of children. If swallowed, 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 for guidance.

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. Remember, it's always better to be safe and check with a professional if you suspect an overdose.

Pregnancy Use

If you are pregnant or planning to become pregnant, it is important to avoid using this medication. The safety of salicylic acid during pregnancy has not been established, which means that its effects on your developing baby are unclear. You should only consider using it if it is clearly necessary and if the potential benefits outweigh any risks to your fetus (unborn baby). Always consult with your healthcare provider before making any decisions regarding medication during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that there is no specific information available regarding the use of this medication during lactation (the period of breastfeeding). This means that the effects on milk production or the 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 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, 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 drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication should be used if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help you understand how to manage your treatment effectively while considering your kidney health.

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 share your complete list of medications and any health conditions you have to receive the best care possible.

Storage and Handling

To ensure the safety and effectiveness of your product, it’s important to store it properly. Keep the bottle tightly capped and store it at room temperature, ideally between 20°C to 30°C (68°F to 86°F). Make sure to keep it away from any sources of heat, fire, or flame to prevent any hazards.

When handling the product, always prioritize safety by ensuring that it remains in a stable environment. Proper storage and careful handling will help maintain the quality and integrity of the product for your use.

Additional Information

No further information is available.

FAQ

What is Liquid Corn & Callus Remover used for?

Liquid Corn & Callus Remover is used for the removal of corns and calluses, relieving pain by safely removing them.

How should I apply Liquid Corn & Callus Remover?

Wash the affected area and dry it thoroughly. Apply one drop at a time with the applicator to cover each corn or callus, and let it dry.

How often can I use this product?

You can repeat the application once or twice daily as needed for up to 14 days, or until the corn or callus is removed.

Are there any contraindications for using this product?

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

What should I do if discomfort persists while using this product?

If discomfort persists, see your doctor or podiatrist.

Is Liquid Corn & Callus Remover safe to use during pregnancy?

The safety of salicylic acid during pregnancy has not been established; use only if clearly needed and the potential benefits justify the potential risk to the fetus.

What precautions should I take when using this product?

Avoid contact with eyes and inhaling vapors. If the product gets into your eyes, flush with water for 15 minutes.

How should I store Liquid Corn & Callus Remover?

Cap the bottle tightly and store it at room temperature away from heat, between 20°C to 30°C (68°F to 86°F).

What should I do if the product is swallowed?

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

Is there any information on drug interactions?

No drug interactions information is provided for Liquid Corn & Callus Remover.

Packaging Info

Below are the non-prescription pack sizes of Salicylic Acid (liquid corn and callus 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 and calluses. It provides relief from pain associated with these conditions by effectively removing the corns and calluses.

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. One drop of the product should be applied at a time using the provided applicator, ensuring that each corn or callus is sufficiently covered. After application, the area should be allowed to dry completely.

To relieve pressure on the treated area, it is recommended to use cushions with a hole centered over the corn or callus. Additional cushions may be purchased separately if needed.

This procedure may be repeated once or twice daily as necessary, for a maximum duration of 14 days, or until the corn or callus is removed.

Contraindications

Use is contraindicated in the following situations:

Application on irritated skin is prohibited due to the potential for exacerbation of the condition. The product should not be applied to any area that is infected or reddened, as this may lead to further complications. Additionally, use is contraindicated in patients with diabetes, given the increased risk of adverse effects. Patients with poor blood circulation should also avoid use, as this may impair healing and increase the risk of complications.

Warnings and Precautions

For external use only, this product is flammable; therefore, it must be kept away from fire or flame. It is essential to cap the bottle tightly and store it at room temperature, away from heat sources.

This product should not be used on irritated skin or on any area that is infected or reddened. Additionally, individuals with diabetes or poor blood circulation should refrain from using this product.

When utilizing this product, if discomfort persists, it is advised to consult a healthcare professional, such as a doctor or podiatrist. Care should be taken to avoid contact with the eyes and to prevent inhalation of vapors. In the event that the product comes into contact with the eyes, it is crucial to flush the eyes with water for at least 15 minutes.

To ensure safety, this product must be kept out of reach of children. In the case of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center should be made without delay.

Side Effects

Patients should be aware that this product is for external use only. It is contraindicated for use on irritated skin, any area that is infected or reddened, and in individuals with diabetes or poor blood circulation.

During the use of this product, if discomfort persists, patients are advised to consult their doctor or podiatrist. It is important to avoid contact with the eyes and to refrain from inhaling vapors. In the event that the product comes into contact with the eyes, it should be flushed with water for 15 minutes.

Additionally, this product should be kept out of reach of children. If swallowed, patients should seek medical assistance or contact a Poison Control Center immediately.

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 Salicylic Acid (liquid corn and callus 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

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. As such, 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 efficacy, given the lack of targeted data for this population.

Pregnancy

The use of salicylic acid is contraindicated in pregnant patients or those planning to become pregnant. The safety of salicylic acid during pregnancy has not been established, and its use should be considered only if clearly needed, with a careful assessment of the potential benefits versus the risks to the fetus. Healthcare professionals are advised to counsel women of childbearing potential regarding these risks and to explore alternative treatment options when appropriate.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or its effects on lactation. Additionally, no data are provided concerning the excretion of the drug in breast milk or its potential effects on breastfed infants. Healthcare professionals should consider the lack of information when advising lactating mothers about the use of this medication.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the drug insert text regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the lack of data necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

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 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 product out of reach of children to prevent accidental ingestion. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use the product on irritated skin or on any area that is infected or reddened. It is also important to counsel patients against using the product if they are diabetic or have poor blood circulation, as these conditions may increase the risk of adverse effects.

While using the product, patients should be advised to monitor for any discomfort. If discomfort persists, they should consult their doctor or podiatrist for further evaluation.

Healthcare providers should emphasize the importance of avoiding contact with the eyes and inhaling vapors from the product. In the event that the product does come into contact with the eyes, patients should be instructed to flush the eyes with water for at least 15 minutes and seek medical attention if irritation continues.

Storage and Handling

The product is supplied in a tightly capped bottle. It is essential to store the bottle at room temperature, ensuring it is kept away from heat sources. The recommended storage temperature range is between 20°C to 30°C (68°F to 86°F). Additionally, it is crucial to keep the product away from fire or flame to maintain safety and integrity.

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.