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Sanuscode Wart Remover

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Active ingredient
Salicylic Acid 17 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2026
Label revision date
February 5, 2026
Active ingredient
Salicylic Acid 17 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 2026
Label revision date
February 5, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-050

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If you are a consumer or patient please visit this version.

Drug Overview

You may be dealing with common or plantar warts, which are growths on the skin caused by a virus. Common warts typically have a rough, “cauliflower-like” appearance, while plantar warts are found on the bottom of the foot and can be tender, often disrupting your footprint pattern.

This medication is specifically designed to help remove these types of warts, providing a solution for those looking to eliminate these skin growths. If you're experiencing discomfort or concern about warts, this treatment could be a helpful option for you.

Uses

You can use this treatment to remove common and plantar warts. Common warts are easily identified by their rough, “cauliflower-like” appearance on the skin. On the other hand, plantar warts occur only on the bottom of the foot, where they can be tender and disrupt your footprint pattern.

This treatment is effective for these types of warts, helping you regain smooth skin without the worry of any harmful effects during pregnancy or other nonteratogenic (not causing birth defects) concerns.

Dosage and Administration

To start treating your wart, first wash the affected area thoroughly. You may find it helpful to soak the wart in warm water for about 5 minutes to soften it. After that, use a cotton swab to apply a sufficient amount of the medication, ensuring that each wart is completely covered.

Once applied, allow the medication to dry. You should repeat this process once or twice a day as needed, continuing until the wart is removed. This treatment can be used for up to 12 weeks, so be patient and consistent for the best results.

What to Avoid

It's important to use this medication safely. You should not use it on irritated skin or any area that appears infected or reddened. Additionally, avoid applying it to moles, birthmarks, or warts—especially those with hair growing from them, as well as genital warts or warts on the face or mucous membranes.

If you have diabetes or poor blood circulation, you should also refrain from using this product. Following these guidelines helps ensure your safety and the effectiveness of the treatment.

Side Effects

This product is intended for external use only. If you experience any discomfort while using it, it's important to stop using the product and consult with a doctor. Persistent discomfort should also prompt you to seek medical advice. Your health and safety are a priority, so don’t hesitate to reach out to a healthcare professional if you have any concerns.

Warnings and Precautions

This product is for external use only. If you accidentally swallow it, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

Avoid using this product on irritated skin, infected areas, or any skin conditions such as moles, birthmarks, or warts (especially those with hair, genital warts, or warts on the face). If you have diabetes or poor blood circulation, do not use it. If you experience ongoing discomfort while using this product, stop using it and consult your doctor.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's important to be aware of the general signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it is 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

When considering the use of SANUSCODE WART REMOVER (which contains 17% salicylic acid) during pregnancy, it's important to note that there is no available information about its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that the effects of this product on you or your developing baby are not well understood.

If you are pregnant or planning to become pregnant, it is advisable to consult with your healthcare provider before using this product. They can help you weigh the potential risks and benefits based on your specific situation. Always prioritize your health and the health of your baby when making decisions about treatments.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into your breast milk, and the effects on your nursing infant have not been thoroughly studied. Therefore, exercising caution is recommended to ensure the safety and well-being of both you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should seek medical help immediately or contact a Poison Control Center at 1-800-222-1222. Taking quick action can be crucial in ensuring their safety. Always be vigilant and store medications securely to prevent any accidents.

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 before starting the medication. 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 particularly true if your kidneys are not functioning as well as they should be. Regular monitoring of your kidney function tests is essential to ensure your safety and the effectiveness of your treatment.

If your creatinine clearance (a measure of how well your kidneys filter waste) is less than 30 mL/min, you may require a reduced dose of your medication. Always consult with your healthcare provider to determine the best approach for your specific situation.

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.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help determine the best approach based on your liver function and overall health.

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 health conditions you have to receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to keep it away from excessive heat, specifically temperatures above 37°C (99°F), as this can affect its effectiveness.

When handling the product, always do so with clean hands and in a clean environment to maintain its integrity. If you have any specific disposal instructions, be sure to follow them carefully to ensure safety.

Additional Information

You will apply this medication topically, which means you will apply it directly to the skin. You should repeat this application once or twice daily as needed until the wart is removed, but do not use it for more than 12 weeks. If you have any questions about how to use this medication, 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 and plantar warts.

How can I identify a common wart?

A common wart is easily recognized by its rough, 'cauliflower-like' appearance on the surface.

What are the characteristics of a plantar wart?

A plantar wart is located only on the bottom of the foot, is tender, and interrupts the footprint pattern.

How should I apply the wart remover?

Wash the affected area, soak the wart in warm water for 5 minutes, then use a cotton swab to apply a sufficient amount to cover each wart and let it dry.

How often can I use the wart remover?

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

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

Do not use it on irritated skin, infected areas, moles, birthmarks, genital warts, or warts on the face or mucous membranes.

What should I do if discomfort persists?

Stop use and ask a doctor if discomfort persists.

Is this drug safe for use during pregnancy?

There is no specific information regarding the safety of this drug during pregnancy.

What should nursing mothers do before using this product?

Nursing mothers should consult a healthcare professional before using this product due to potential excretion in breast milk.

What precautions should be taken for patients with renal impairment?

Dosage adjustments may be necessary for patients with reduced renal function, and renal function tests should be monitored regularly.

How should I store this drug?

Store at room temperature and avoid excessive heat above 37°C (99°F).

What should I do if the product is swallowed?

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

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 Sanuscode Wart Remover (salicylic acid 17% wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sanuscode Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Sanuscode 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 removal of common and plantar warts. Common warts are characterized by their rough, “cauliflower-like” appearance on the surface, while plantar warts are specifically located on the bottom of the foot, presenting with tenderness and an interruption of the footprint pattern.

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. Following this, a sufficient amount of the medication should be applied using a cotton swab to ensure complete coverage of each wart. After application, the treated area should be allowed to dry.

This procedure may be repeated once or twice daily as necessary, continuing until the wart is removed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use is contraindicated in the following situations:

Application on irritated skin or any area that is infected or reddened is prohibited due to the potential for exacerbating the condition.

The product should not be applied to moles, birthmarks, warts with hair growth, genital warts, or warts located on the face or mucous membranes, as these areas may be sensitive or require specialized treatment.

Additionally, individuals with diabetes or poor blood circulation should avoid use, as these conditions may increase the risk of adverse effects.

Warnings and Precautions

For external use only. In the event of accidental ingestion, immediate medical assistance should be sought by contacting a Poison Control Center at 1-800-222-1222.

This product is contraindicated for use on irritated skin or any area that is infected or reddened. It should not be applied to moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes. Additionally, individuals with diabetes or poor blood circulation should refrain from using this product.

If discomfort persists after application, the user should discontinue use and consult a healthcare professional for further evaluation and guidance.

Side Effects

For external use only. Patients are advised to stop use and consult a doctor if discomfort persists. This recommendation is crucial to ensure safety and address any potential underlying issues that may arise during treatment.

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 Sanuscode Wart Remover (salicylic acid 17% wart remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sanuscode 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 Poison Control Center (1-800-222-1222) 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 potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

There is currently no information available regarding the use of SANUSCODE WART REMOVER (salicylic acid 17% wart remover liquid) during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in women who are pregnant or may become pregnant. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes in the absence of specific data.

Lactation

Nursing mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are not well studied; therefore, caution is advised.

Renal Impairment

Dosage adjustments may be necessary for patients with reduced renal function. It is important to monitor renal function tests regularly in patients with known kidney problems. A reduced dose should be considered in patients with a creatinine clearance of less than 30 mL/min.

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. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Continuous monitoring of vital signs and clinical status is essential to ensure patient safety.

Healthcare professionals should also consider consulting a poison control center or relevant toxicology resources for guidance on management strategies tailored to the specific circumstances of the overdosage event.

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

Skin discoloration has been reported in postmarketing experience, occurring during or after the use of the product. These events were documented through voluntary reports and surveillance programs.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center at 1-800-222-1222 if the product is swallowed. It is important for patients to understand that they should discontinue use and consult a doctor if discomfort persists.

Patients should be cautioned to avoid contact with their eyes. In the event that the product comes into contact with the eyes, they should flush the area with water for at least 15 minutes. Additionally, healthcare providers should instruct patients to avoid inhaling vapors associated with the product.

Providers should emphasize the importance of securely closing the cap after use and storing the product at room temperature, away from heat sources, to ensure safety and efficacy.

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 at room temperature, ensuring that it is kept away from excessive heat, defined as temperatures exceeding 37°C (99°F). Proper storage conditions are crucial to maintain the integrity and efficacy of the product.

Additional Clinical Information

The medication is administered topically, with the recommended frequency being once or twice daily 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 Sanuscode 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 Sanuscode 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.