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Folupia Liquid Wart Corn Remover

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This product has been discontinued

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 2025
Label revision date
October 4, 2025
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 2025
Label revision date
October 4, 2025
Manufacturer
Jiangxi Hemei Pharmaceutical Co. , Ltd
Registration number
M028
NDC root
84010-193

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Drug Overview

Salicylic acid is a medication commonly 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.

This treatment helps to effectively eliminate these types of warts, providing relief and improving the appearance of the affected skin. If you're dealing with warts, salicylic acid may be a suitable option to consider.

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, areas that are infected or reddened, or on moles, birthmarks, or warts—especially those with hair growing from them, genital warts, or warts on the face or mucous membranes. Additionally, if you have diabetes or poor blood circulation, you should avoid using this product altogether.

Using this medication improperly can lead to serious issues, including potential dependence (a condition where your body becomes reliant on a substance). Always follow these guidelines to ensure your safety and well-being.

Side Effects

When using this product, it's important to remember that it is for external use only and is flammable, so keep it away from fire and flames. If you experience any discomfort that doesn't go away, please stop using the product and consult your doctor for further advice. Your safety and well-being are the top priority, so don't hesitate to seek medical guidance if needed.

Warnings and Precautions

This product is for external use only and is flammable, so be sure to keep it away from fire and flames. If you accidentally swallow it, seek medical help immediately or contact the Poison Control Center at 1-800-222-1222.

If you experience any discomfort that continues, please stop using the product and reach out to your doctor for further advice. Your safety is important, so don’t hesitate to seek help if needed.

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 that you or someone else may have taken too much of this medication, it’s crucial to seek immediate medical help.

In case of an overdose, do not wait for symptoms to appear. Contact your healthcare provider or local emergency services right away. They can provide the necessary assistance and guidance to ensure safety. Always keep medications out of reach and follow the prescribed dosage to prevent any potential risks.

Pregnancy Use

When it comes to using this product during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before using this product. They can help you understand any potential risks and make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding any medications or treatments during this important time.

Lactation Use

If you are breastfeeding, you can use this product without specific warnings or recommendations against it. Currently, there is no information available about whether this product passes into breast milk or if it poses any risk to your nursing infant. Always feel free to consult with your healthcare provider if you have any concerns or questions about using medications while breastfeeding.

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 the Poison Control Center at 1-800-222-1222. Acting quickly can help ensure your child's safety.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, be sure to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach for your individual health needs, especially since older adults may have different responses to medications compared to younger individuals. Always keep an open line of communication with your doctor about any changes in health or medication effects.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines, dosage adjustments, or monitoring recommendations provided for your condition in the available information. This means that the standard instructions for the medication do not include special considerations for those with renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is 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 differently due to your liver health.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver function and how it relates to your treatment. They can help ensure that your medication is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, your healthcare provider can help ensure that your treatment is safe and effective, especially if you are taking other medications or have underlying health conditions. Always feel free to ask questions and share your complete health history to get 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 care to maintain its integrity. If you have any specific components that come with the product, make sure to follow any additional instructions provided for their use and safety. Proper storage and handling will help you get the most out of your device.

Additional Information

You will apply this treatment topically, meaning you will apply it directly to the skin. You should repeat this process once or twice daily as needed until the wart is removed, but do not use it for more than 12 weeks.

It's important to avoid getting the product in your eyes. If it does happen, flush your eyes with water for 15 minutes. If you accidentally swallow the product, seek medical help immediately or contact the Poison Control Center at 1-800-222-1222.

FAQ

What is Salicylic acid used for?

Salicylic acid is used for the removal of common warts and plantar warts.

What do common and plantar warts look like?

Common warts have a rough 'cauliflower-like' surface, while plantar warts are located on the soles of the feet and are tender to touch with an interrupted footprint pattern.

How should I apply Salicylic acid?

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 Salicylic acid on irritated skin, infected areas, moles, birthmarks, or genital warts. Avoid using it 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.

Is Salicylic acid safe to use during pregnancy?

The insert does not provide specific information regarding the use of Salicylic acid during pregnancy.

What should I do if I swallow Salicylic acid?

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

How should I store Salicylic acid?

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

Can I use Salicylic acid if I am nursing?

There are no specific warnings or recommendations regarding the use of Salicylic acid by nursing mothers.

What are the warnings associated with Salicylic acid?

Salicylic acid is for external use only, is flammable, and should be kept away from fire and flame.

Packaging Info

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

Packaging configurations for Folupia Liquid Wart Corn Remover.
Details

Drug Information (PDF)

This file contains official product information for Folupia Liquid Wart Corn 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 and plantar warts. Common warts are characterized by a rough, "cauliflower-like" surface and are easily recognizable. 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 to ensure complete coverage of each wart. It is important to allow the application to dry fully.

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; this product is flammable and should be kept away from fire and flame.

In the event of accidental ingestion, it is imperative to seek emergency medical assistance immediately or contact the Poison Control Center at 1-800-222-1222.

Healthcare professionals should advise patients to discontinue use and consult a physician if discomfort persists.

Side Effects

Patients should be aware that the product is for external use only and is flammable; it should be kept away from fire and flame. In the event that discomfort persists, patients are advised to stop using the product and consult a doctor. This recommendation is crucial to ensure safety and address any potential adverse reactions that may arise during use.

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 Folupia Liquid Wart Corn Remover (salicylic acid 17% liquid wart corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Folupia Liquid Wart Corn 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 therapeutic response, given the lack of targeted data for this population.

Pregnancy

The available prescribing information does not provide specific data regarding the use of this product during pregnancy. Consequently, there are no established safety concerns, dosage modifications, or special precautions outlined for pregnant patients. Healthcare professionals should exercise caution when considering the use of this product in women of childbearing potential and weigh the potential risks and benefits. It is advisable to monitor for any adverse fetal outcomes in the absence of specific data.

Lactation

There are no specific warnings or recommendations regarding the use of this product by lactating 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 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 specific guidance necessitates careful clinical judgment.

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. If symptoms of overdosage are observed, appropriate interventions should be implemented based on the clinical presentation.

Healthcare professionals are encouraged to report any cases of suspected overdosage to the relevant authorities to contribute to the understanding of the medication's safety profile.

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

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

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 about the importance of avoiding contact with the eyes. In the event that the product comes into contact with the eyes, they should be instructed to flush the eyes with water for at least 15 minutes.

It is essential to emphasize that the product is non-edible. Patients should be reminded to keep the cap tightly closed and store 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 the storage environment does not exceed excessive heat, defined as 37°C (99°F). Proper handling should be observed to maintain the integrity of the product throughout its shelf life.

Additional Clinical Information

The product 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. 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. Additionally, if the product is swallowed, patients should seek medical assistance or contact the Poison Control Center immediately at 1-800-222-1222.

No further information is available regarding laboratory tests, abuse potential, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Folupia Liquid Wart Corn 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 Folupia Liquid Wart Corn 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.