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Wart Remover Patchs

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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
May 8, 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
May 8, 2024
Manufacturer
Gaozhou Chapin Technology Co. , Ltd
Registration number
M028
NDC root
84168-015

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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. 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 for dealing with these skin growths.

It's important to note that there are no reported teratogenic effects (which means it does not 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 replace the patch daily to maintain effective treatment. Following this routine will help ensure that you receive the full benefits of the medication.

What to Avoid

It's important to use this medication safely. You should avoid applying it to any areas of your skin that are irritated, infected, or reddened. Additionally, do not use it on genital warts, warts on the face, moles, birthmarks, or warts that have hair growing from them. It's also crucial to keep it away from mucous membranes, which are the moist tissues lining certain body parts, such as your mouth and nose. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

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 listed, you should be aware that any product can potentially cause skin irritation or allergic reactions. If you experience any unusual symptoms after using it, consult 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 usage guidelines provided to ensure safety and effectiveness.

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 any irritated, infected, or reddened skin, as well as to avoid using it on genital warts, facial warts, moles, birthmarks, or warts with hair growing from them. Additionally, do not use it on mucous membranes (the moist tissue lining certain body cavities).

Before using this product, consult your doctor if you have diabetes or poor blood circulation, as these conditions may affect how the product works for you. Always prioritize your safety and well-being when using any medication.

Overdose

If you suspect an overdose of this medication, it's important to stay calm and take immediate action. While the drug insert does not provide specific information about overdose, you should be aware of general signs that may indicate an overdose, such as unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or have concerns about a possible overdose, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get professional advice in these situations.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that the potential risks and benefits have not been clearly established for pregnant individuals.

If you are pregnant or planning to become pregnant, it’s important to discuss any medications you are considering with your healthcare provider. They can help you understand the best options for your health and the health of 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 you breastfeed). This means that the effects on breast milk or your nursing infant are not clearly defined.

If you are breastfeeding and considering using this product, it’s important to consult with your healthcare provider to discuss any potential risks and to ensure the safety of 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 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 there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

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 liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

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 and safety of your product, store it in a cool, dry place where the temperature remains between 59°F and 86°F (15°C and 30°C). This temperature range helps maintain the integrity of the device.

When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage. Always keep it in a clean environment to ensure it remains safe for use. If you have any questions about disposal or further handling, please refer to the guidelines provided with your product.

Additional Information

You should apply the medication 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 use the medicated patch?

Wash the affected area, dry it thoroughly, and apply the medicated patch. Repeat the procedure every 48 hours as needed for up to 12 weeks.

Are there any contraindications for this drug?

Yes, 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 patch?

If swallowed, seek medical help or contact a Poison Control Center immediately.

Is this drug safe for use during pregnancy?

No specific information regarding safety during pregnancy is provided in the drug insert.

What are the storage conditions for this drug?

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

Can I use this drug if I have diabetes?

You should ask a doctor before use if you have diabetes or poor blood circulation.

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 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 related to SPL code 34089-3 are provided in the text.

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

Healthcare professionals are advised to administer one patch of tolnaftate 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 to minimize skin irritation and to avoid applying the patch to broken or irritated skin.

Contraindications

Use is contraindicated in the following situations:

Application is not recommended on irritated, infected, or reddened skin 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 specific sensitivities. Additionally, it is contraindicated for use on moles, birthmarks, and warts with hair growing from them, as these may require specialized care. The product must not be applied to mucous membranes, given the risk of irritation or adverse reactions in these sensitive areas.

Warnings and Precautions

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

The product is contraindicated for application on irritated, infected, or reddened skin. It should not be used on genital warts, facial warts, moles, birthmarks, or warts that exhibit hair growth. Additionally, application on mucous membranes is strictly prohibited.

Healthcare professionals are advised to consult with a physician prior to recommending this product to patients who have diabetes or exhibit poor blood circulation, as these conditions may increase the risk of adverse effects.

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 should be monitored for any signs of irritation or allergic reactions upon application.

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

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

There is no specific information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of effective contraception during treatment.

Lactation

There is no specific information 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

Patients with renal impairment have not been specifically addressed in the available data 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 information necessitates careful clinical judgment and monitoring.

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 regarding its safety and efficacy in this population. Regular monitoring of liver function may be warranted based on clinical judgment.

Overdosage

In the absence of specific information regarding overdosage in the available sections of the drug insert, healthcare professionals are advised to exercise caution and consider general principles of management for suspected overdosage cases.

Recommended Actions In the event of an overdosage, it is essential to assess the patient's clinical status and initiate supportive care as necessary. Monitoring vital signs and providing symptomatic treatment should be prioritized.

Potential Symptoms While specific symptoms related to overdosage are not detailed, healthcare professionals should remain vigilant for any unusual or severe reactions that may arise, given the lack of documented information.

Management Procedures Healthcare providers should follow standard protocols for managing drug overdosage, which may include activated charcoal administration if appropriate and the implementation of supportive measures tailored to the patient's needs. Consultation with a poison control center or a medical toxicologist is recommended for further guidance in managing suspected overdosage cases.

In summary, due to the absence of specific overdosage information, healthcare professionals should rely on established clinical practices and their clinical judgment when addressing potential overdosage scenarios.

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 question.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

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 discussion is essential to ensure the safe and effective use of the medication, taking into account any underlying health conditions that may affect treatment.

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 the 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 further 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.

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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.