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Dermfree Wart Remover

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This product has been discontinued

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 2025
Label revision date
November 13, 2025
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 2025
Label revision date
November 13, 2025
Manufacturer
Jiangxi Hemei Pharmaceutical Co. , Ltd
Registration number
M028
NDC root
84010-217

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Drug Overview

You may be looking for a treatment for common warts, which are easily recognized by their rough, 'cauliflower-like' appearance. This medication is specifically designed to help remove these warts, providing a solution for those who may find them bothersome or unsightly.

By targeting the wart itself, this treatment works to eliminate the growth, helping you regain smoother skin. If you're dealing with common warts, this medication could be a helpful option to consider.

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

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 medicated plaster sticks 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

It's important to use this medication safely to avoid potential complications. 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 unwanted side effects and may worsen your condition. Always follow these guidelines to ensure your safety and the effectiveness of your treatment.

Side Effects

It's important to note that this product is for external use only. If you have diabetes or poor blood circulation, you should consult with your doctor before using it. This is to ensure your safety and to avoid any potential complications. Always prioritize your health and seek professional advice if you have any concerns.

Warnings and Precautions

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

Before using this product, it's important to consult with your doctor if you have diabetes or experience poor blood circulation, as these conditions may affect how the product works for you. Always prioritize your health and safety by discussing any concerns with your healthcare provider.

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 signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, call your local emergency number or go to the nearest hospital. Always keep medications out of reach of children 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 specific information available about the use of DERMFREE WART REMOVER (which contains salicylic acid 1%) during pregnancy. The insert does not mention any safety concerns, dosage changes, or special precautions for pregnant individuals.

As always, it's best to consult with your healthcare provider before using any medication during pregnancy to ensure it is safe for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to talk to your healthcare professional before using this product. There is a possibility that the ingredients could pass into your breast milk, so caution is advised. Since the effects on your nursing infant have not been thoroughly studied, it's essential to weigh the potential risks against the benefits of using this product. Your healthcare provider can help you make an informed decision that prioritizes both your health and your baby's well-being.

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 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 is safe and effective, especially if you have any concerns about your kidney health. They can provide guidance based on your individual situation.

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 if you have hepatic impairment (liver issues).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

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 share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

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 keep it in a clean environment to avoid contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal. By taking these precautions, you can help ensure the product works effectively and safely.

Additional Information

You will apply this treatment topically, meaning you will apply it directly to the skin. 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 drug used for?

The 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 medication?

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

How often should I apply the medicated plaster?

You should repeat the procedure every 48 hours as needed until the wart is removed, 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, or warts on the face.

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

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

What should I do if the product is swallowed?

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

Is it safe to use this product during pregnancy?

There is no specific information regarding the use of this product during pregnancy, so consult a healthcare professional.

Can nursing mothers use this product?

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

How should I store this medication?

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

What should I do if I experience side effects?

If you experience any side effects or have concerns, consult your healthcare provider for advice.

Packaging Info

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

Packaging configurations for Dermfree Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Dermfree Wart 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 drug.

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

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 can 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 is contraindicated on irritated, infected, or reddened skin due to the potential for exacerbation of the condition. Application is also contraindicated on genital warts and warts located on the face, as well as on moles, birthmarks, and warts with hair growing from them, to prevent adverse reactions. Additionally, the product should not be applied to mucous membranes, as this may lead to irritation or other complications.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to consult a physician prior to use if they have a history of diabetes or poor blood circulation, as these conditions may increase the risk of adverse effects.

In the event of accidental ingestion, it is imperative to seek emergency medical assistance or contact a Poison Control Center immediately. Prompt action is crucial to ensure patient safety.

Patients should be instructed to discontinue use and consult their healthcare provider if they experience any concerning symptoms or if they have pre-existing conditions such as diabetes or poor blood circulation. Monitoring for any adverse reactions is recommended to ensure safe usage.

Side Effects

For external use only. Patients are advised to stop use and consult a doctor if they have diabetes or poor blood circulation prior to using the product. It is important for individuals with these conditions to seek medical advice before use to ensure safety and efficacy.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Dermfree Wart 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 the local 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 elderly patients closely for any potential adverse effects or changes in efficacy, given the lack of targeted data for this population. Consideration of individual patient factors, including comorbidities and concurrent medications, is essential in managing treatment in elderly patients.

Pregnancy

There is no information available regarding the use of DERMFREE WART REMOVER (salicylic acid 1%) during pregnancy. The prescribing information does not indicate any safety concerns, dosage modifications, or special precautions for pregnant patients. Healthcare professionals should consider the lack of data when advising women of childbearing potential about the use of this product during pregnancy.

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 effects on the nursing infant are not well studied; thus, the risks versus benefits should be considered.

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 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 unusual symptoms or adverse effects that may arise. In the event of suspected overdosage, it is recommended to initiate supportive care and symptomatic treatment as necessary.

Healthcare providers should consider contacting a poison control center for guidance on management strategies tailored to the specific situation. Continuous assessment of the patient's clinical status is essential to ensure appropriate interventions are implemented promptly.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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 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 the temperature range of 59° to 86°F (15° to 30°C) to maintain its efficacy and stability. 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 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. 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 Dermfree Wart 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 Dermfree Wart 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.

Learn more in our Editorial Policy

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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.