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Komxsum Wart Remover Patches

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Active ingredient
Salicylic Acid 1 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
March 24, 2026
Active ingredient
Salicylic Acid 1 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
March 24, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-171

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Drug Overview

You may be looking for a solution to remove common warts, which are easily identified by their rough, 'cauliflower-like' appearance. This medication is specifically designed for the effective removal of these warts, helping to restore the skin's smoothness and appearance.

If you're dealing with common warts, this treatment can provide a straightforward option to address them. It's important to follow the instructions for use to achieve the best results.

Uses

You can use this medication to help remove common warts, which are easily identified by their rough, 'cauliflower-like' surface. This treatment is specifically designed for this purpose, making it a straightforward option if you're dealing with these types of warts.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects associated with this medication. This makes it a safe choice for those looking to address common warts without additional concerns.

Dosage and Administration

To start treating your wart, first wash the affected area by soaking it in warm water for about 5 minutes. After soaking, make sure to dry the area thoroughly to ensure the medication adheres properly.

Next, take the medicated patch and remove the bandage strips by peeling off the backing. If the patch is too large for your wart, you can cut it to fit. Carefully apply the medicated plaster directly onto the wart. You should repeat this process every 48 hours as needed, continuing until the wart is removed, but not exceeding a total of 12 weeks.

What to Avoid

You should avoid using this product on any irritated, infected, or reddened skin, as well as on genital warts and warts located on the face. It's also important not to apply it to moles, birthmarks, or warts with hair growing from them, especially on mucous membranes.

If you notice any irritation or infection while using the product, or if you are treating genital warts, facial warts, or any of the aforementioned skin conditions, please stop using it immediately. Your safety is important, so always follow these guidelines to prevent any adverse effects.

Side Effects

This product is intended for external use only. You should stop using it if you notice any irritation, infection, or redness on your skin. It is also important to avoid applying it to genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them, especially on mucous membranes.

If you accidentally swallow this product, seek medical help immediately or contact a Poison Control Center for assistance.

Warnings and Precautions

This product is for external use only. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately. It's important not to apply this product to irritated, infected, or reddened skin, as well as to genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them on mucous membranes.

If you notice any irritation, infection, or redness after using the product, stop using it right away and consult your doctor. Additionally, if you have diabetes or poor blood circulation, please ask your doctor before using this product to ensure it's safe for you.

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 potential risks associated with taking more than the recommended dose. If you suspect an overdose, you may experience symptoms such as unusual drowsiness, confusion, or difficulty breathing.

In the event of an overdose, it is crucial to seek immediate medical attention. You should contact your healthcare provider or go to the nearest emergency room right away. If possible, bring the medication container with you to help medical professionals understand what you've taken. Always remember that it's better to be safe and get help if you have any concerns about your health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be cautious with any medications or treatments, including salicylic acid wart remover patches. Currently, there is no specific information available about the safety of using these patches during pregnancy, which means that potential risks or necessary dosage adjustments have not been established.

To ensure your safety and the health of your baby, it’s best to consult with your healthcare provider before using any wart removal products while pregnant. They can provide personalized advice and help you explore safer alternatives if needed.

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 KOMXSUM WART REMOVER PATCHES during nursing. This means that the effects on breast milk and nursing infants have not been studied or documented.

As a precaution, you may want to consult with your healthcare provider before using this product to ensure it is safe for you and your baby. Your health and your baby's well-being are the top priorities, so getting professional advice can help you make the best decision.

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 for personalized advice. 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 your medication dosage may need to be adjusted. This is because renal impairment can affect how your body processes certain drugs. Your healthcare provider will likely monitor your renal function tests regularly to ensure your kidneys are working properly.

If you have decreased creatinine clearance (a measure of kidney function), your doctor may recommend a reduced dose of your medication to avoid potential side effects. Always communicate openly with your healthcare team about your kidney health to ensure safe and effective treatment.

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.

It's always best to discuss your liver condition with your healthcare provider before starting any new medication. They can provide personalized advice and ensure that your treatment 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. 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 a temperature between 59°F and 86°F (15°C and 30°C). This temperature range helps maintain the integrity and effectiveness of the device.

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 affected area. You can repeat the application every 48 hours as needed until the wart is removed, but do not use it for more than 12 weeks. If you have any questions about the treatment process, be sure to consult with your healthcare provider for guidance.

FAQ

What is the purpose of this drug?

This drug is used for the removal of common warts, which are easily recognized by their rough 'cauliflower-like' appearance.

How should I prepare the wart before applying the medicated patch?

You should wash the affected area, soak the wart in warm water for 5 minutes, and then dry the area thoroughly.

How often should I apply the medicated patch?

You should repeat the procedure every 48 hours as needed until the wart is removed, for up to 12 weeks.

Are there any areas where I should not use this drug?

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 I accidentally swallow the drug?

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

Is this drug safe to use during pregnancy?

The insert does not provide specific information regarding the use of this drug during pregnancy.

What should I do if I have diabetes or poor blood circulation?

You should ask a doctor before using this drug if you have diabetes or poor blood circulation.

How should I store this drug?

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

What should I do if I experience irritation after using the drug?

You should stop using the drug if you experience irritation, infection, or reddening of the skin.

Is there any information about the use of this drug in elderly patients?

No specific information regarding geriatric use or dosage adjustments for elderly patients is provided.

Packaging Info

Below are the non-prescription pack sizes of Komxsum Wart Remover Patches (salicylic acid 1% wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Komxsum Wart Remover Patches.
Details

Drug Information (PDF)

This file contains official product information for Komxsum Wart Remover Patches, 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 common warts, which are characterized by their rough, 'cauliflower-like' surface appearance.

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

Dosage and Administration

The affected area should be washed, and it is recommended to soak the wart in warm water for approximately 5 minutes. After soaking, the area must be dried thoroughly to ensure proper adhesion of the medicated plaster.

To apply the medicated plaster, healthcare professionals should first remove the bandage strips by peeling the backing off. If necessary, the medicated patch may be cut to fit the size of the wart. The plaster should then be carefully applied to the wart.

This procedure may be repeated every 48 hours as needed, continuing until the wart is removed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use of this product is contraindicated in the following situations:

Application is not recommended on irritated, infected, or reddened skin due to the potential for exacerbating these conditions. Additionally, the product should not be applied to genital warts or warts located on the face, as these areas may be more sensitive and prone to adverse reactions. Furthermore, the use of this product is contraindicated on moles, birthmarks, and warts with hair growing from them, particularly on mucous membranes, to avoid irritation and complications.

If any of these conditions develop during use, discontinue application immediately.

Warnings and Precautions

For external use only. In the event of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

This product is contraindicated for application on irritated, infected, or reddened skin. It should not be used on genital warts, warts located on the face, moles, birthmarks, or warts with hair growing from them, particularly on mucous membranes.

If any of the aforementioned conditions arise during use, the application should be discontinued immediately.

Healthcare professionals should advise patients to consult a physician prior to use if they have diabetes or experience poor blood circulation, as these conditions may necessitate additional precautions or alternative treatment options.

Side Effects

For external use only. Patients are advised to discontinue use if irritation, infection, or redness occurs on the skin. The product should not be applied to genital warts, warts on the face, moles, birthmarks, or warts with hair growing from them, particularly on mucous membranes.

In the event of accidental ingestion, 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 Komxsum Wart Remover Patches (salicylic acid 1% wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Komxsum Wart Remover Patches.
Details

Pediatric Use

Pediatric patients should be advised to keep the 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 available 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

The safety of salicylic acid wart remover patches during pregnancy has not been established, as the prescribing information does not provide specific data regarding their use in this population. Consequently, healthcare professionals are advised to exercise caution when considering the use of these patches in pregnant patients. There are no available studies or risk categories that delineate potential fetal impacts or safety concerns associated with the use of salicylic acid in this context. Therefore, it is recommended that women of childbearing potential discuss any potential risks with their healthcare provider before using this product during pregnancy.

Lactation

There is no information available regarding the use of KOMXSUM WART REMOVER PATCHES in lactating mothers or its effects on breastfed infants. Healthcare professionals should consider this lack of data when advising lactating patients.

Renal Impairment

Patients with renal impairment may require dosage adjustments to ensure safety and efficacy. It is essential to monitor renal function tests in individuals with kidney problems to assess their renal status. Additionally, a reduced dose should be considered for patients with decreased creatinine clearance to mitigate the risk of adverse effects associated with impaired renal function.

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

There is currently no specific information available regarding overdosage for this medication. Healthcare professionals are advised to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Patients should be evaluated for potential complications, and appropriate interventions should be implemented based on the clinical presentation.

For further guidance, healthcare professionals may refer to established protocols for managing drug overdosage or consult a poison control center.

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 compound in these areas.

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 medication is swallowed. It is crucial for patients to understand the importance of prompt action in such situations.

Additionally, healthcare providers should encourage patients to consult with their doctor prior to using the medication if they have a history of diabetes or poor blood circulation. This precaution is essential to ensure the safe and effective use of the medication in these specific health conditions.

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° to 86°F (15° 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, with the procedure to be repeated every 48 hours as needed until the wart is removed, for a maximum duration of 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 Komxsum Wart Remover Patches, 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 Komxsum Wart Remover Patches, 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.