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Sylvirene Liquid Wart Corn Callus 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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2026
Label revision date
February 9, 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
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2026
Label revision date
February 9, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-069
Packaging Info
Packaging & NDC Codes

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

Drug Overview

This medication is used for the removal of common warts and plantar warts. Common warts are easily recognizable due to their rough, "cauliflower-like" surface, while plantar warts occur on the soles of the feet and can be tender to touch, often displaying an interrupted footprint pattern.

If you are dealing with these types of warts, this treatment can help you effectively remove them and restore the appearance of your skin.

Uses

You can use this medication to help remove common warts and plantar warts. Common warts are easily identifiable by their rough, "cauliflower-like" surface, while plantar warts specifically appear on the soles of your feet. These plantar warts can be tender when touched and often have a unique interrupted pattern resembling a footprint.

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.

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 soaking, make sure to dry the area completely.

Next, use a cotton swab to apply a sufficient amount of the medication to cover each wart. Allow the medication to dry completely. You should repeat this process once or twice a day as needed, continuing until the wart is removed, but not exceeding 12 weeks of treatment.

What to Avoid

It's important to be cautious when using this medication. You should not use it on irritated skin or any areas that are infected or reddened. Additionally, avoid applying it to moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes.

If you have diabetes or poor blood circulation, you should also not use this medication, as it may pose additional risks. Always prioritize your health and consult with a healthcare professional if you have any concerns or questions about its use.

Side Effects

It's important to be aware of some key warnings and recommendations regarding this product. It is for external use only, so please avoid contact with fire and flames. If you experience any discomfort while using it, you should stop using the product and consult a doctor, especially if the discomfort continues. Your health and safety are paramount, so don't hesitate to seek medical advice if needed.

Warnings and Precautions

This product is for external use only, so please keep it away from fire and flames. Avoid using it on irritated skin or any areas that are infected or reddened. It should not be applied to moles, birthmarks, warts with hair, genital warts, or warts on the face or mucous membranes. If you have diabetes or poor blood circulation, it's best to consult your doctor before use.

If you accidentally swallow this product, seek emergency medical help immediately or contact the Poison Control Center at 1-800-222-1222. Additionally, if you experience ongoing discomfort while using this product, stop using it and reach out to your doctor for advice.

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’s crucial to seek immediate medical help.

In case of an emergency, you should 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 are no specific contraindications (conditions that would prevent use) or safety concerns mentioned regarding the use of this medication during pregnancy. Additionally, there are no dosage modifications required for pregnant individuals, and no special precautions have been noted.

While this information suggests that the medication may be safe to use during pregnancy, it's always best to consult with your healthcare provider before starting any new medication. They can provide personalized advice based on your health and circumstances.

Lactation Use

When it comes to breastfeeding, there is currently no specific information available regarding the use of this medication for nursing mothers or its effects during lactation (the period of breastfeeding). This means that if you are breastfeeding, it’s important to consult with your healthcare provider for personalized advice and to discuss any potential risks or considerations related to your situation. Always prioritize your health and the well-being of your baby when making decisions about medication use while breastfeeding.

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 the Poison Control Center at 1-800-222-1222. Taking quick action can help ensure their safety. Always be vigilant about where you store medications to prevent any accidental ingestion.

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 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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 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

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

To use this treatment effectively, start by washing the affected area and soaking the wart in warm water for about 5 minutes. After drying the area thoroughly, apply a sufficient amount of the product with a cotton swab to cover each wart. Allow it to dry and repeat this process once or twice daily as needed, up to a maximum of 12 weeks until the wart is removed.

It's important to avoid contact with your eyes; if the product does get into your eyes, flush them with water for 15 minutes. Remember, this product is not edible, so keep it tightly capped and store it at room temperature, away from heat. If you accidentally swallow it, seek medical help or contact the Poison Control Center at 1-800-222-1222 immediately.

FAQ

What is the drug used for?

The drug is used for the removal of common warts and plantar warts.

What do common warts look like?

Common warts have a rough 'cauliflower-like' surface and are easily recognizable.

Where are plantar warts located?

Plantar warts are located only on the soles of the feet and are tender to touch, often showing an interrupted footprint pattern.

How should I apply the drug?

Wash the affected area, soak the wart in warm water for 5 minutes, dry it thoroughly, and use a cotton swab to apply a sufficient amount to cover each wart. Let it dry and repeat once or twice daily as needed for up to 12 weeks.

Are there any precautions I should take?

Do not use the drug on irritated skin, infected areas, moles, birthmarks, or genital warts. Avoid use if you have diabetes or poor blood circulation.

What should I do if I experience discomfort?

Stop use and ask a doctor if discomfort persists.

What should I do if the drug is swallowed?

If swallowed, get medical help or contact the Poison Control Center at 1-800-222-1222 immediately.

How should I store the drug?

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

Is it safe to use during pregnancy?

No specific information regarding safety during pregnancy is provided, but no teratogenic effects are mentioned.

Can I use this drug if I am nursing?

There is no specific information provided regarding the use of this drug while nursing.

Packaging Info

Below are the non-prescription pack sizes of Sylvirene Liquid Wart Corn Callus Remover (salicylic acid 17% liquid wart corn callus remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sylvirene Liquid Wart Corn Callus Remover.
Details

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for the removal of common warts and plantar warts. Common warts are characterized by a rough, "cauliflower-like" surface and are easily identifiable. Plantar warts are specifically located on the soles of the feet, presenting as tender to touch and exhibiting an interrupted 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, the wart may be soaked in warm water for approximately 5 minutes. After soaking, the area must be dried completely.

A sufficient amount of the medication should be applied using a cotton swab, ensuring that each wart is adequately covered. It is important to allow the application to dry completely.

This procedure may be repeated once or twice daily as needed, continuing until the wart is removed, for a maximum duration of 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; it is imperative to keep the product away from fire and flame to prevent any potential hazards.

General precautions must be observed to ensure safe application. The product should not be used on irritated skin or any area that is infected or reddened. It is contraindicated for application on 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 avoid using this product.

In the event of accidental ingestion, immediate medical assistance should be sought. Contact the Poison Control Center at 1-800-222-1222 without delay.

If discomfort persists after application, it is advised to discontinue use and consult a healthcare professional for further evaluation and guidance.

Side Effects

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

In the event that discomfort persists, it is advised that patients stop using the product and consult a healthcare professional. This recommendation is crucial to ensure safety and address any underlying issues that may arise during 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 Sylvirene Liquid Wart Corn Callus Remover (salicylic acid 17% liquid wart corn callus remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Sylvirene Liquid Wart Corn Callus 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

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

The use of this medication during pregnancy has not been explicitly addressed in the available data. There are no known contraindications for its use in pregnant patients, and no safety concerns have been identified regarding its administration during pregnancy. Additionally, there are no recommended dosage modifications for pregnant individuals, nor are there any special precautions indicated for use in this population. Healthcare professionals should consider the overall clinical context when prescribing this medication to women of childbearing potential.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or its effects on lactation. Additionally, no data are provided concerning the excretion of this medication in breast milk or its potential effects on breastfed infants. Healthcare professionals should consider the lack of information when advising lactating mothers about the use of this medication.

Renal Impairment

Patients with renal impairment may not have specific dosage adjustments, special monitoring, or safety considerations outlined in the prescribing information. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function is advisable to ensure patient safety and therapeutic efficacy.

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 signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Patients should be evaluated for potential complications, and appropriate interventions should be implemented based on the clinical presentation.

For further guidance, healthcare professionals should refer to established protocols and consult relevant toxicology resources.

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 seek immediate medical assistance or contact the Poison Control Center at 1-800-222-1222 if the product is swallowed.

Patients should be informed to avoid contact with the eyes. In the event that the product does come into contact with the eyes, they should flush the eyes with water for at least 15 minutes and seek medical attention if irritation persists.

It is important to emphasize that the product is non-edible. Patients should be instructed to keep the product tightly capped and stored 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 should be stored at room temperature, ensuring that the temperature does not exceed 37°C (99°F) to avoid excessive heat exposure. Proper storage conditions are essential to maintain the integrity of the product.

Additional Clinical Information

Patients should wash the affected area and may soak the wart in warm water for 5 minutes before thoroughly drying the area. A sufficient amount of the product should be applied using a cotton swab to cover each wart, allowing it to dry. This procedure may be repeated once or twice daily as needed until the wart is removed, for a maximum duration of 12 weeks.

Clinicians should counsel patients to avoid contact with the eyes. In the event of contact, the eye should be flushed with water for 15 minutes. The product is non-edible, and patients should ensure the cap is tightly closed and stored at room temperature, away from heat. If ingested, patients are advised to seek medical assistance or contact the Poison Control Center at 1-800-222-1222 immediately.

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 Sylvirene Liquid Wart Corn Callus 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.