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Sanuscode Wart Corn Remover

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Active ingredient
Salicylic Acid 40 g/100 1
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2026
Label revision date
February 4, 2026
Active ingredient
Salicylic Acid 40 g/100 1
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 2026
Label revision date
February 4, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-049

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Drug Overview

This medication is used for the removal of warts and corns, which are common skin growths that can be bothersome. It works by targeting the affected areas to help eliminate these skin issues, providing relief and improving the appearance of your skin. If you're dealing with warts or corns, this treatment may be a suitable option to consider for effective removal.

Uses

You can use this medication to help remove warts and corns from your skin. Warts are small growths caused by a virus, while corns are thickened areas of skin that often develop on your feet due to pressure or friction.

It's important to note that this medication does not have any known effects that could harm a developing fetus (teratogenic effects), so it is considered safe in that regard. If you have any questions about using this treatment, be sure to consult with your healthcare provider.

Dosage and Administration

To start treating your wart, first wash the affected area thoroughly. You can soak the wart in warm water for about 5 minutes to help soften it, but this step is optional. After washing, make sure to dry the area completely.

Next, if the medicated plaster is too large, you can cut it to fit the size of your wart. Once it’s the right size, apply the plaster directly onto the wart. You should repeat this process every 48 hours as needed, and you can continue this treatment for up to 12 weeks.

What to Avoid

It's important to use this medication safely. You should not use it on any irritated, infected, or reddened skin. Additionally, avoid applying it to genital warts, warts on the face, moles, birthmarks, or warts that have hair growing from them. Using the medication in these areas can lead to complications or worsen your condition. Always follow these guidelines to ensure your safety and the effectiveness of the treatment.

Side Effects

It's important to note that this product is for external use only. If you experience any discomfort that continues or worsens, please stop using the product and consult a doctor. Additionally, if you have diabetes or poor blood circulation, it's advisable to speak with your doctor before using this product to ensure it's safe for you.

Warnings and Precautions

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

If you experience any discomfort that continues or worsens after using this product, stop using it and reach out to your doctor for advice. Your health and safety are important, so don’t hesitate to seek help if needed.

Overdose

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

In case of an emergency, you should call your local emergency number or go to the nearest hospital. Always keep your medications in a safe place and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

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

Before taking this medication, you should discuss it with your healthcare provider to understand any potential risks and to ensure the best care for you and your baby. 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 consult with your healthcare professional before using this product. There is a possibility that it may be excreted in breast milk, which means caution is advised. The safety of this product during lactation has not been fully established, so it's essential to keep an eye on your infant for any potential adverse effects while using it. Your healthcare provider can help you weigh the benefits and risks to ensure the best outcome for both 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, 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 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 information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

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 temperatures between 59°F and 86°F (15°C and 30°C). 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

You will apply this medication topically, meaning you will apply it directly to the skin. You can repeat the application every 48 hours as needed, but do not use it for more than 12 weeks. If you have any questions about how to use this medication or its effects, be sure to consult with your healthcare provider.

FAQ

What is this drug used for?

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

How should I apply the medicated plaster?

First, wash the affected area and dry it thoroughly. If needed, cut the plaster to fit the wart, then apply it and repeat every 48 hours as needed, for up to 12 weeks.

Are there any teratogenic effects associated with this drug?

No teratogenic effects are mentioned for this drug.

Can I use this drug on any skin?

Do not use it on irritated, infected, or reddened skin, genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them.

What should I do if discomfort persists?

Stop use and ask a doctor if discomfort persists or worsens.

Is this drug safe to use during pregnancy?

No specific information regarding safety during pregnancy is provided, so consult a healthcare professional.

What precautions should nursing mothers take?

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

What should I do if I accidentally swallow this drug?

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

How should I store this drug?

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

Is this drug for external use only?

Yes, this drug is for external use only.

Packaging Info

Below are the non-prescription pack sizes of Sanuscode Wart Corn Remover (salicylic acid 40% wart corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sanuscode Wart Corn Remover.
Details

Drug Information (PDF)

This file contains official product information for Sanuscode Wart Corn Remover, 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 warts and corns.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

The affected area should be washed thoroughly. Soaking the wart in warm water for 5 minutes is optional but may enhance the effectiveness of the treatment. After washing, the area must be dried completely.

If necessary, the medicated plaster can be cut to fit the size of the wart. The plaster should then be applied directly to the wart.

This application should be repeated every 48 hours as needed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use is contraindicated on irritated, infected, or reddened skin due to the potential for exacerbation of the condition. Application is also contraindicated on genital warts, facial warts, moles, birthmarks, or warts with hair growing from them, as these areas may be sensitive and could lead to adverse reactions. Additionally, the product should not be applied to mucous membranes, given the risk of irritation and other complications.

Warnings and Precautions

For external use only. This product is not intended for ingestion. In the event of accidental swallowing, it is imperative to seek medical assistance immediately or contact a Poison Control Center.

Healthcare professionals should advise patients to discontinue use and consult a physician if discomfort persists or worsens. Continuous monitoring of the patient's condition is recommended to ensure safety and efficacy.

In cases of ingestion, prompt emergency medical help is essential. Immediate action should be taken to mitigate any potential adverse effects associated with swallowing the product.

Side Effects

For external use only. Patients are advised to stop use and consult a doctor if discomfort persists or worsens. Additionally, individuals with diabetes or poor blood circulation should seek medical advice before using this product.

Drug Interactions

There are currently no documented drug interactions associated with the use of 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 Sanuscode Wart Corn Remover (salicylic acid 40% wart corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sanuscode Wart Corn Remover.
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 a 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. Therefore, 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

There is no information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential risks and benefits. Women of childbearing potential should be counseled accordingly.

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 nursing mothers. The safety of this product during lactation has not been established. It is recommended to monitor breastfed infants for any adverse effects if the nursing mother uses this product.

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

There is currently no specific information available regarding overdosage for this medication. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Continuous monitoring of vital signs and clinical status is essential. If symptoms of overdosage are observed, appropriate interventions should be implemented based on the patient's condition.

Healthcare professionals should also consider contacting a poison control center or a medical toxicologist for guidance on management strategies tailored to the specific situation.

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.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important to inform patients that the product should not be applied to irritated, infected, or reddened skin, as well as on genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them, and on mucous membranes.

Patients should be instructed to discontinue use and consult a doctor if discomfort persists or worsens. Additionally, healthcare providers should emphasize the importance of avoiding contact with the eyes or face. In the event that the product comes into contact with the eyes, patients should rinse thoroughly with water.

Furthermore, patients with diabetes or poor blood circulation should be encouraged to consult a doctor before using the product to ensure safety and appropriateness.

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 59°F to 86°F (15°C to 30°C) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable environment to prevent degradation.

Additional Clinical Information

The medication is administered topically and may be repeated every 48 hours as needed, for a duration of up to 12 weeks. 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 Sanuscode Wart Corn Remover, 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 Sanuscode Wart Corn Remover, 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.