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Sottsunfeli Wart Remover

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Active ingredient
Salicylic Acid 15 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
November 14, 2025
Active ingredient
Salicylic Acid 15 g/100 mL
Other brand names
Dosage form
Liquid
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 14, 2025
Manufacturer
Henan Toudaorong Biotechnology Co. , Ltd.
Registration number
M028
NDC root
85136-010

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Drug Overview

This medication is used to treat warts, which are small growths on the skin caused by a virus. It works by applying a solution directly to the wart, which helps to remove it over time. To use it, you should first wash the affected area and may soak the wart in warm water for about five minutes. After drying the area thoroughly, you apply the medication with a brush to ensure it covers the wart completely. This process can be repeated once or twice daily as needed, and treatment can continue for up to 12 weeks until the wart is removed.

Uses

To treat warts, start by washing the affected area thoroughly. You can soak the wart in warm water for about 5 minutes to help soften it. After drying the area completely, use a brush to apply a sufficient amount of the treatment to cover each wart, allowing it to dry afterward. You should repeat this process once or twice daily as needed until the wart is removed, which may take up to 12 weeks.

It's important to follow these steps consistently for the best results. If you have any concerns or questions about the treatment, consider reaching out to a healthcare professional for guidance.

Dosage and Administration

To start treating your wart, first, wash the affected area thoroughly to ensure it's clean. You can enhance the treatment by soaking the wart in warm water for about 5 minutes. This helps to soften the wart, making it easier for the medication to work effectively.

After preparing the area, follow the specific instructions provided for applying the treatment. Remember to be consistent with your application to achieve the best results.

What to Avoid

You can feel confident using this medication, as there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with it. This means that, based on the available information, there are no known reasons that would prevent you from taking this medication safely. Always remember to follow your healthcare provider's guidance and reach out if you have any questions or concerns about your treatment.

Side Effects

When using this product, it's important to remember that it is for external use only and is flammable, so you should keep it away from fire and flames. Always handle it with care to avoid any potential hazards.

Warnings and Precautions

This product is intended for external use only, so please avoid using it on any internal areas of your body. It is also flammable, which means you should keep it away from fire and flames to prevent any accidents.

If you experience any unusual reactions or have concerns while using this product, stop use immediately and contact your doctor for guidance. Always prioritize your safety and well-being when using any medical product.

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 unusual drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, contact your local poison control center 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 be cautious with the use of salicylic acid. The safety of this ingredient during pregnancy has not been established, and it is generally advised against due to potential risks to your developing baby, including possible teratogenic effects (which means it could cause developmental issues).

Before using any products containing salicylic acid, you should consult with your healthcare provider. They can provide guidance tailored to your specific situation and help you make informed decisions about your skincare during pregnancy.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

It's important to keep this product out of reach of children to ensure their safety. Remember, this medication is for external use only and is flammable, so handle it with care.

If you're using it for a wart, you can apply it once or twice daily as needed until the wart is removed, but do not use it for more than 12 weeks. Always monitor your child during treatment to ensure they are using it safely and effectively.

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 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).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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

It's important to store this product safely by keeping it out of reach of children. Remember, this product is for external use only and is flammable, so you should avoid exposing it to fire or flames.

When handling the product, always prioritize safety by ensuring that it is used in a well-ventilated area and away from any potential sources of ignition. Following these guidelines will help you use the product effectively while minimizing any risks.

Additional Information

No further information is available.

FAQ

How should I apply this drug to warts?

First, wash the affected area and soak the wart in warm water for 5 minutes. Dry the area thoroughly, then use a brush to apply a sufficient amount to cover each wart and let it dry.

How often should I repeat the application?

You should repeat the application once or twice daily as needed until the wart is removed, for up to 12 weeks.

Are there any contraindications for using this drug?

There are no contraindications listed for this drug.

Is this drug safe to use during pregnancy?

The safety of this drug during pregnancy has not been established, and it is contraindicated due to potential risks to the fetus.

What precautions should I take if I am pregnant?

Consult a healthcare professional before using this product if you are pregnant or planning to become pregnant.

Can I use this drug while nursing?

There are no specific warnings or recommendations regarding the use of this product in nursing mothers.

What should I know about the drug's flammability?

This drug is for external use only and is flammable, so keep it away from fire and flame.

What should I do if I have children?

Keep this drug out of reach of children.

Packaging Info

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

Packaging configurations for Sottsunfeli Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Sottsunfeli 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 specified drug.

Uses and Indications

This drug is indicated for the topical treatment of warts. Prior to application, the affected area should be washed and, if desired, the wart may be soaked in warm water for 5 minutes. The area must be dried thoroughly before application. A sufficient amount of the drug should be applied using a brush to ensure complete coverage of each wart, and the application should be allowed to dry. This procedure may be repeated once or twice daily as needed until the wart is removed, with a maximum treatment duration of up to 12 weeks.

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

Dosage and Administration

The affected area should be washed thoroughly prior to treatment. For optimal results, it is recommended to soak the wart in warm water for approximately 5 minutes. This preparation step may enhance the effectiveness of subsequent treatment measures.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence.

Warnings and Precautions

The product is intended for external use only and is classified as flammable. It is imperative that healthcare professionals advise patients to keep the product away from fire and flame to prevent any potential hazards associated with its use. Proper storage and handling instructions should be emphasized to ensure safety during application.

Side Effects

Patients should be aware that the product is for external use only and is flammable. It is imperative to keep the product away from fire and flame to prevent any potential hazards.

No specific adverse reactions have been reported in clinical trials or postmarketing experiences beyond the warnings related to its flammability and external use. Therefore, patients are advised to adhere strictly to the usage guidelines to minimize risks associated with improper use.

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 Sottsunfeli Wart Remover (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sottsunfeli Wart Remover.
Details

Pediatric Use

Pediatric patients should be advised to keep this product out of reach of children. It is intended for external use only and is flammable. The recommended application procedure may be repeated once or twice daily as needed until the wart is removed, with a maximum duration of use of up to 12 weeks.

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

Pregnancy

The safety of salicylic acid during pregnancy has not been established, and its use is contraindicated due to potential risks to the fetus. There may be risks associated with the use of salicylic acid during pregnancy, including potential teratogenic effects. Pregnant women should avoid the use of salicylic acid unless directed by a healthcare provider. It is essential for women of childbearing potential to consult a healthcare professional before using this product if they are pregnant or planning to become pregnant.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in 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

In the absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, increased severity of known side effects, unusual behavioral changes, or any other atypical clinical manifestations.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. It is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for specific guidance on the management of overdose cases.

In summary, while specific overdosage data is not available, healthcare professionals should exercise caution, remain observant for potential overdose symptoms, and implement appropriate management strategies as needed.

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 to keep the medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage to ensure the safety of young children.

Storage and Handling

This product is supplied in packaging that ensures safety and compliance with handling requirements. It is essential to keep this product out of reach of children to prevent accidental ingestion or misuse.

For storage, the product must be kept in a cool, dry place, away from sources of ignition, as it is flammable. It is crucial to avoid exposure to fire and flame to maintain safety during storage and handling. The product is intended for external use only, and all precautions should be taken to adhere to these guidelines.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Sottsunfeli 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 Sottsunfeli 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.

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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.