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Codecure 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 7, 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 7, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-078

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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 eliminate 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 use this product safely to avoid potential complications. You should never apply it to irritated skin, areas that are infected or reddened, or on moles, birthmarks, or warts that have hair growing from them. Additionally, avoid using it on genital warts or warts located on the face or mucous membranes. If you have diabetes or poor blood circulation, do not use this product.

While using the product, be careful to keep it away from your eyes. If it accidentally gets into your eye, rinse it thoroughly with water for 15 minutes. Always prioritize your safety and well-being when using any medical product.

Side Effects

It's important to note that this product is for external use only. If you experience any discomfort that continues, please stop using the product and consult a doctor for further advice. Your health and safety are paramount, so don't hesitate to seek professional guidance if needed.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any areas that are irritated, infected, or reddened. It's important not to use it on moles, birthmarks, or warts that have hair growing from them, as well as genital warts or warts on the face and mucous membranes. If you have diabetes or poor blood circulation, you should also refrain from using this product.

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

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 in doubt, it’s better to err on the side of caution and seek assistance.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no available information about the safety or use of CODECURE WART REMOVER (which contains 17% salicylic acid) during pregnancy. This means that there are no specific guidelines, dosage adjustments, or precautions provided for pregnant individuals.

Given the lack of information, it is advisable to consult with your healthcare provider before using this product to ensure the safety of both you and your baby. Always prioritize open communication with your doctor regarding any treatments you are considering 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. Currently, there is also no information available about whether this product is excreted in breast milk or any potential risks to your infant.

As always, it's a good idea to consult with your healthcare provider if you have any concerns or questions about using this product while breastfeeding. Your health and the health of your baby are important, and your provider can help you make informed decisions.

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 these precautions can help ensure your child's safety.

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 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 is safe and effective for your specific condition. They can help determine the best approach for managing your health, especially if you have concerns about your kidneys.

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. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual’s health situation is unique, and your provider can help ensure that your treatment plan is safe and effective for you. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

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, meaning you will apply it directly to the skin. You can 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.

FAQ

What is this drug used for?

This drug 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 the wart remover?

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 contraindications for using this product?

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

What should I do if I accidentally get the product in my eyes?

If the product gets into your eyes, flush with water for 15 minutes.

What should I do if discomfort persists?

Stop use and ask a doctor if discomfort persists.

Is this product safe for use during pregnancy or while nursing?

There is no specific information regarding the use of this product during pregnancy or in nursing mothers.

What should I do if I swallow this product?

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

How should I store this product?

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

Is this product for external use only?

Yes, this product is for external use only.

Packaging Info

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

Packaging configurations for Codecure Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Codecure 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 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, are tender to touch, and exhibit 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 of this product is contraindicated in the following situations:

Application is not recommended on irritated skin or any area that is infected or reddened, as this may exacerbate the condition. The product should not be applied to moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes due to the potential for adverse reactions. Additionally, individuals with diabetes or poor blood circulation should avoid use, as these conditions may increase the risk of complications.

Warnings and Precautions

For external use only. This product is contraindicated for application on irritated skin or any area that exhibits signs of infection or redness. It is also not recommended for use on moles, birthmarks, or warts that have hair growing from them, as well as genital warts or warts located on the face or mucous membranes.

Patients with diabetes or those who have poor blood circulation should refrain from using this product due to the increased risk of adverse effects.

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.

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

Side Effects

For external use only. Patients should discontinue use and consult a doctor if discomfort persists.

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

Packaging configurations for Codecure 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 CODECURE WART REMOVER (salicylic acid 17% wart remover liquid) during pregnancy. This includes any safety concerns, dosage modifications, or special precautions that may be necessary for pregnant patients. Due to the lack of data, healthcare professionals are advised to exercise caution when considering the use of this product in women who are pregnant or may become pregnant. It is recommended that the potential risks and benefits be carefully evaluated before administration in this population.

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

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 is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

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 clinical judgment.

For further guidance, healthcare professionals may refer to established protocols for managing drug overdosage or consult a poison control center.

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.

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. It is important for patients to understand the seriousness of this action and to act promptly.

Patients should be instructed to discontinue use and consult a doctor if they experience persistent discomfort after using the product. This ensures that any potential adverse effects are addressed in a timely manner.

Providers must emphasize the importance of avoiding contact with the eyes. In the event that the product does come into contact with the eyes, patients should be advised to flush the affected eye with water for at least 15 minutes and seek medical attention if irritation persists.

Additionally, healthcare providers should remind patients that the product is non-edible. They should be instructed to keep the cap tightly closed and store the product at room temperature, away from heat sources, to maintain its efficacy and safety.

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, specifically 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 Codecure 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 Codecure 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.