ADD CONDITION

items per page

Wart Remover Patchs

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Salicylic Acid 200 mg/1 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
June 25, 2024
Active ingredient
Salicylic Acid 200 mg/1 g
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 2024
Label revision date
June 25, 2024
Manufacturer
Gaozhou Chapin Technology Co. , Ltd
Registration number
M028
NDC root
84168-015

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

You may be looking for a solution to remove common warts, which are easily recognized 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. Always consult with a healthcare professional for guidance on the best approach for your situation.

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 for dealing with these skin growths.

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

When using this medication, you will apply one patch each day. Each patch contains 1 mg of tolnaftate, which is an antifungal medication used to treat certain skin infections. Make sure to place the patch on clean, dry skin for the best results.

Remember to change the patch daily, ensuring that you do not apply more than one patch at a time. Following these instructions will help you effectively manage your condition.

What to Avoid

It's important to use this medication safely to avoid potential complications. You should not use it on any irritated, infected, or reddened skin, as well as on genital warts or warts located on the face. Additionally, avoid applying it to moles, birthmarks, or warts that have hair growing from them, and do not use it on mucous membranes (the moist tissue lining certain body parts).

By following these guidelines, you can help ensure your safety and the effectiveness of the treatment. If you have any questions or concerns about where to apply the medication, please consult your healthcare provider for personalized advice.

Side Effects

It's important to note that this product is for external use only, meaning it should not be ingested or applied internally. While specific side effects are not detailed here, you should be aware that any unusual reactions or discomfort should be reported to your healthcare provider.

For best results, store the product in a cool, dry place, ideally between 59°F and 86°F (15°C and 30°C). Always follow the guidance of your healthcare professional regarding its use.

Warnings and Precautions

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

Before using this product, it's important to consult your doctor if you have diabetes or experience poor blood circulation. If you notice any unusual symptoms or have concerns while using the product, stop using it and reach out to your healthcare provider for guidance.

Overdose

If you suspect an overdose, it's important to stay calm and take action. While there is no specific information available about the effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe an overdose has occurred, seek immediate medical help. It's always better to err on the side of caution when it comes to your health. Remember, if you're ever in doubt, contacting a healthcare professional is the best course of action.

Pregnancy Use

If you are pregnant or planning to become pregnant, it’s important to be cautious with certain treatments. This product should not be used on genital warts or warts on the face. Additionally, it is intended for external use only, so avoid applying it to any internal areas. Always consult with your healthcare provider before using any medication during pregnancy to ensure it is safe for you and your baby.

Lactation Use

There is no specific information available about the use of WART REMOVER PATCHES for nursing mothers or during lactation (the period when a mother breastfeeds her baby). This means that the effects of the product on breast milk or nursing infants have not been studied or documented.

If you are breastfeeding and considering using this product, it’s important to consult with your healthcare provider to discuss any potential risks or concerns. They can help you make an informed decision that prioritizes your health and the well-being of 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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it’s important to discuss any potential risks and benefits with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for your condition in the provided information. This means that the standard recommendations for medication use may apply to you, but it's always best to consult with your healthcare provider for personalized advice. They can help ensure that any medications you take are safe and effective for your specific health needs.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help monitor your liver function and determine the best course of action for your treatment.

Make sure to keep your doctor informed about your liver health, as they may need to conduct regular tests to ensure your safety while using any medication. Your well-being is a priority, so don't hesitate to ask questions or express any concerns you may have.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking or lab tests you may undergo. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that this medication is generally considered safe to use alongside other treatments and tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions and share your complete list of medications and health concerns during your appointments.

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 product's effectiveness and safety.

When handling the product, be sure to keep it in a clean environment to avoid contamination. Always follow any specific instructions provided for use and disposal to ensure safety and effectiveness.

Additional Information

You should apply this treatment topically, repeating the procedure every 48 hours as needed until the wart is removed, but not exceeding 12 weeks. If you have diabetes or poor blood circulation, it's important to consult with your doctor before using this product.

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 apply the medicated patch?

You should wash the affected area, soak the wart in warm water for 5 minutes, dry it thoroughly, and then carefully apply the medicated plaster. Repeat this procedure every 48 hours as needed for up to 12 weeks.

Are there any warnings I should be aware of?

Yes, this product is for external use only. 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.

What should I do before using this drug?

You should ask a doctor before use 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) and keep it out of reach of children.

Is there any information about using this drug during pregnancy or while nursing?

No specific information regarding teratogenic effects during pregnancy or use while nursing is provided in the drug insert.

Packaging Info

Below are the non-prescription pack sizes of Wart Remover Patchs (wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Wart Remover Patchs.
Details

Drug Information (PDF)

This file contains official product information for Wart Remover Patchs, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No specific description details are available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the removal of common warts, which are characterized by their rough, 'cauliflower-like' surface appearance.

Limitations of Use: There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

Healthcare professionals are advised to administer one patch per day. Each patch contains 1 mg of tolnaftate. The patch should be applied to clean, dry skin, ensuring that it adheres properly. It is important to rotate the application site with each new patch to minimize skin irritation.

Contraindications

Use of this product is contraindicated in the following situations:

Application on irritated, infected, or reddened skin is prohibited due to the potential for exacerbating the condition. The product should not be used on genital warts or warts located on the face, as these areas may have different sensitivities and risks associated with treatment. Additionally, the application on moles, birthmarks, or warts with hair growing from them is contraindicated to avoid potential complications. Finally, the use of this product on mucous membranes is not recommended, as it may lead to irritation or adverse reactions.

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 emergency medical assistance or contact a Poison Control Center immediately.

Patients should discontinue use and consult their healthcare provider if they have diabetes or experience poor blood circulation prior to using this product. It is essential to discuss any underlying health conditions with a physician to ensure safe usage.

Side Effects

For external use only. Patients should be advised to store the product between 59° and 86°F (15° and 30°C) to maintain its efficacy and safety.

No specific adverse reactions have been reported in clinical trials or postmarketing experiences. However, as with any topical product, patients may experience localized reactions such as irritation or allergic responses. It is essential for patients to monitor for any adverse effects and consult a healthcare professional if they occur.

Drug Interactions

There are no specified drug interactions associated with this medication. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the available data.

Packaging & NDC

Below are the non-prescription pack sizes of Wart Remover Patchs (wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Wart Remover Patchs.
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

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 adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should be advised that this product is contraindicated for use on genital warts and warts on the face. The safety of this product during pregnancy has not been established, and it is recommended that healthcare professionals exercise caution when considering its use in pregnant patients. The product is intended for external use only, and potential risks to fetal outcomes have not been fully characterized. Therefore, women of childbearing potential should be informed of these considerations and advised to consult their healthcare provider for alternative treatment options if necessary.

Lactation

There is no specific information available regarding the use of WART REMOVER PATCHS in lactating mothers or its effects on breastfed infants. Healthcare professionals should consider the absence of data when advising lactating mothers about the use of this product.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney 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 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 context of overdosage, there is currently no specific information available regarding the effects or management of an overdose for this medication. Healthcare professionals are advised to monitor patients closely for any unusual symptoms or adverse reactions that may arise.

In the absence of detailed overdosage data, it is recommended that standard supportive measures be employed. This includes ensuring the patient's safety, providing symptomatic treatment, and considering the use of activated charcoal if the ingestion occurred within a suitable timeframe.

Healthcare providers should remain vigilant and report any observed adverse effects to the appropriate regulatory authorities to contribute to the ongoing assessment of the medication's safety profile.

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 that if the medication is swallowed, it is crucial to seek medical help or contact a Poison Control Center immediately. This information is vital for ensuring patient safety and prompt action in case of accidental ingestion. Providers should emphasize the importance of acting quickly and not waiting for symptoms to appear, as timely intervention can be critical.

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 efficacy and integrity. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable environment to prevent degradation.

Additional Clinical Information

The product 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. Clinicians should advise patients to consult a doctor prior to use if they have diabetes or poor blood circulation. No additional information is available regarding laboratory tests, abuse potential, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Wart Remover Patchs, 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 Wart Remover Patchs, 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.