ADD CONDITION

items per page

Cure-Aid Corn Plasters

Last content change checked dailysee data sync status

Active ingredient
Salicylic Acid 40 mg
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2014
Label revision date
January 7, 2025
Active ingredient
Salicylic Acid 40 mg
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 2014
Label revision date
January 7, 2025
Manufacturer
Pharmaplast SAE
Registration number
M030
NDC root
28691-4000

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 conditions as it works to effectively remove the corns and calluses.

The treatment comes with an adhesive bandage that keeps the medicated pad securely in place, ensuring that it works effectively while you go about your day. This combination of features makes it a convenient option for managing these common skin issues.

Uses

If you're dealing with corns and calluses, this treatment can help you 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 product comes with an adhesive bandage that keeps the medicated pad securely in place, ensuring that you get the most benefit from the treatment while you go about your day.

Dosage and Administration

To start treating your corn, first wash the affected area with soap and water, then dry it thoroughly. Once the area is clean and dry, apply a medicated bandage specifically designed for corn treatment.

After 48 hours, you should remove the medicated bandage. If the corn is still present, you can repeat this process every 48 hours as needed, but do not continue for more than 14 days. To help with the removal of the corn, you may soak it in warm water for about 5 minutes before applying the bandage again. This can make the corn easier to treat.

What to Avoid

It's important to keep this medication out of reach of children to prevent accidental ingestion. If you or someone else swallows it, seek medical help immediately or contact a Poison Control Center for assistance.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always use it responsibly and follow any additional guidance from your healthcare provider.

Side Effects

It's important to be aware of some warnings associated with this product. It is for external use only, so you should not use it if you are diabetic or have poor blood circulation. Additionally, avoid applying it to any irritated, infected, or reddened skin. If you experience discomfort that lasts, please stop using the product and consult a doctor.

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, infected, or reddened skin. If you experience discomfort that lasts, it’s important to stop using the product and consult your doctor.

In case of accidental swallowing, seek emergency medical help or contact a Poison Control Center immediately. Always prioritize your health and safety by following these guidelines closely.

Overdose

If you or someone else has swallowed a medication and you suspect an overdose, 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. Always err on the side of caution and get help if you are unsure. Remember, timely action can make a significant difference in ensuring safety and health.

Pregnancy Use

Currently, there is no information available about the use of CURE-AID CORN PLASTERS (salicylic acid patch) during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been established. If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product to ensure it is safe for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the effects of this medication on nursing mothers or lactation (the process of producing breast milk). Since there are no guidelines or data provided, it’s advisable to consult your healthcare provider for personalized advice and to discuss any potential risks or concerns related to your situation. Always prioritize your health and the well-being of your baby when making decisions about medication while breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should seek medical help immediately or contact a Poison Control Center. Taking quick action can be crucial in ensuring their safety. Always be vigilant and store medications securely to prevent any accidents.

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 discuss any concerns you may have regarding your liver function and how it relates to your treatment. They can help ensure that your medication is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, always ensure that your healthcare provider is aware of all the medications you are using, as this helps them provide the best care tailored to your needs.

By discussing your full medical history and any other treatments, you can help prevent potential issues and ensure your safety.

Storage and Handling

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

When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage. Always keep the product away from extreme temperatures and dispose of it according to local regulations to ensure safety and environmental protection.

Additional Information

You will apply the medicated bandage to the affected area after washing and drying it. Make sure to remove the bandage after 48 hours. You can repeat this process every 48 hours as needed, but do not continue for more than 14 days, or until the corn is removed.

FAQ

What is the purpose of this drug?

This drug is used for the removal of corns and calluses.

How does this drug relieve pain?

It relieves pain by removing corns and calluses.

How should I apply the medicated bandage?

Wash the affected area and dry it thoroughly, then apply the medicated bandage.

What should I do after applying the medicated bandage?

Remove the medicated bandage after 48 hours and repeat the procedure every 48 hours as needed for up to 14 days.

Are there any warnings I should be aware of?

Yes, this product is for external use only. Do not use if you are diabetic, have poor blood circulation, or on irritated or infected skin.

What should I do if I accidentally swallow the drug?

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

What should I do if discomfort lasts?

Stop use and ask a doctor if discomfort lasts.

How should I store this drug?

Store between 0º to 40ºC (32º to 104ºF).

Is there any information regarding use during pregnancy or breastfeeding?

No specific information is provided regarding use during pregnancy or breastfeeding.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

Packaging Info

Below are the non-prescription pack sizes of Cure-Aid Corn Plasters (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cure-Aid Corn Plasters.
Details

Drug Information (PDF)

This file contains official product information for Cure-Aid Corn Plasters, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No specific description details are provided in the text.

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 for enhanced efficacy.

Dosage and Administration

The affected area should be washed and dried thoroughly prior to application. A medicated bandage is to be applied directly to the corn. After 48 hours, the medicated bandage must be removed. This procedure may be repeated every 48 hours as needed, for a maximum duration of 14 days, or until the corn is completely removed.

To facilitate the removal of the corn, it is recommended to soak the corn in warm water for 5 minutes before applying the medicated bandage.

Contraindications

Use is contraindicated in the following situations:

  • The product should be kept out of reach of children to prevent accidental ingestion.

  • In the event of accidental swallowing, immediate medical assistance or contact with a Poison Control Center is required.

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 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.

It is imperative that patients are informed of these warnings to ensure safe and effective use of the product.

Side Effects

Patients should be aware that the product is for external use only. It is contraindicated in individuals with diabetes or 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, patients are advised to stop use and consult a healthcare professional.

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Cure-Aid Corn Plasters (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cure-Aid Corn Plasters.
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 contact with a Poison Control Center is recommended.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

There is currently no information available regarding the use of CURE-AID CORN PLASTERS (salicylic acid patch) during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in women who are pregnant or may become pregnant. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes.

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 this medication 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 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 clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the event of an overdosage, immediate medical intervention is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical assistance or contact a Poison Control Center without delay.

Prompt action 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 and management procedures.

Healthcare providers should ensure that patients are aware of the importance of timely reporting of any suspected overdosage to facilitate effective treatment and minimize risks.

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 for SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact a Poison Control Center immediately. This guidance is crucial to ensure the safety and well-being of patients and to mitigate any potential risks associated with accidental ingestion.

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 0º to 40ºC (32º to 104ºF) to maintain its efficacy and safety. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable container that protects it from environmental factors. Special handling requirements should be observed to prevent any compromise to the product's integrity.

Additional Clinical Information

The medication is administered topically. Patients should apply a medicated bandage to the affected area after washing and drying it. The bandage should be removed after 48 hours, and this procedure can be repeated every 48 hours as needed, 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 Cure-Aid Corn Plasters, 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 Cure-Aid Corn Plasters, 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.