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Salicylic acid

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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
January 28, 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
January 28, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-016

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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 your skin's appearance.

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 area that appears 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.

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. If you accidentally swallow it, seek medical help immediately or contact the Poison Control Center at 1-800-222-1222.

Avoid using this product 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 refrain from using it. If you experience ongoing discomfort, stop using the product and consult your doctor.

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 a medication, it’s crucial to seek immediate medical help.

In case of an overdose, contact your local emergency services or go to the nearest hospital. Having the medication packaging or information on hand can help medical professionals provide the best care. Always remember that when it comes to medications, it's better to be safe and get help if you have any concerns.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this product during pregnancy has not been established. While there are no specific contraindications listed, caution is advised since the effects on a developing fetus are unknown. There is also no detailed information available regarding potential risks to the fetus.

Before using this product, you should consult your healthcare provider to discuss any concerns and ensure it is safe for you and your baby. Remember, it's always best to seek professional advice when it comes to medications during pregnancy.

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 it may be excreted in breast milk, which means it could pass to your baby. Since the effects on nursing infants have not been thoroughly studied, it's best to exercise caution. Always prioritize your and your baby's health by seeking professional advice.

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. Taking quick action can help ensure their 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. As you age, your body may process medications differently, which can affect how well they work and the potential for side effects.

If you or a loved one is considering this medication, it’s wise to discuss it with a healthcare provider. They can help determine if any adjustments are needed based on individual health conditions and ensure that the treatment is safe and effective for older adults. Always prioritize open communication with your healthcare team about any concerns or questions you may have.

Renal Impairment

If you have kidney issues, 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 standard recommendations for the medication do not include special monitoring or safety considerations tailored for patients with renal impairment (kidney problems).

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 provide guidance based on your individual 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 feel free to ask questions and share your complete list of medications and any tests you might be undergoing. This way, you can avoid any potential issues and ensure the best possible care.

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 the topical treatment once or twice daily as needed until the wart is removed, for a maximum of 12 weeks. Make sure to follow this schedule closely for the best results. If you have any questions about the treatment process, don't hesitate to reach out to your healthcare provider for guidance.

FAQ

What is this drug used for?

This 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 this 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 this drug on irritated skin, infected areas, moles, birthmarks, or genital warts. If you have diabetes or poor blood circulation, consult a doctor before use.

What should I do if discomfort persists?

Stop use and ask a doctor if discomfort persists.

Is this drug safe to use during pregnancy?

The safety of this product during pregnancy has not been established, so consult a healthcare provider if you are pregnant or planning to become pregnant.

Can nursing mothers use this drug?

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

What should I do if I accidentally swallow this drug?

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

How should I store this drug?

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

Packaging Info

Below are the non-prescription pack sizes of Bitank Liquid Wart Corn Callus Remover. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bitank Liquid Wart Corn Callus Remover.
Details

Drug Information (PDF)

This file contains official product information for Bitank Liquid Wart Corn Callus 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 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. It is recommended to soak the wart in warm water for approximately 5 minutes to facilitate the application process. After soaking, the area must be dried completely.

Using a cotton swab, a sufficient amount of the medication should be applied to ensure complete coverage of each wart. Following 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; this product must be kept away from fire and flame to prevent potential hazards. In the event of accidental ingestion, it is imperative to seek medical assistance immediately or contact the Poison Control Center at 1-800-222-1222.

This product should not be applied to irritated skin or any areas that exhibit signs of infection or redness. It is contraindicated for use on moles, birthmarks, warts with hair growth, genital warts, or warts located on the face or mucous membranes. Additionally, individuals with diabetes or those who have poor blood circulation should avoid using this product.

Should discomfort persist after application, it is essential 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 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 Bitank Liquid Wart Corn Callus Remover. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bitank 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

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 safety of this product during pregnancy has not been established. Caution is advised as the effects on a developing fetus are unknown. There is no specific information available regarding risks to the fetus. No dosage modifications for pregnant individuals are mentioned. It is recommended that pregnant patients or women of childbearing potential consult a healthcare provider before use if they are pregnant or planning to become pregnant.

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

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 clinical trials for 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 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 a medical toxicologist for guidance on management strategies tailored to the individual patient's needs.

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

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 their eyes. In the event that the product comes into contact with the eyes, they should flush the eyes with water for at least 15 minutes.

It is important to emphasize that the product is non-edible. Patients should be instructed to keep the cap tightly closed and store the product at room temperature, away from heat sources.

Healthcare providers should also counsel patients to discontinue use and consult a doctor if any discomfort persists.

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

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 Bitank Liquid Wart Corn Callus 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 Bitank 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.