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Odicut Wart Remover

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Active ingredient
Salicylic Acid 17 g/100 1
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2026
Label revision date
March 16, 2026
Active ingredient
Salicylic Acid 17 g/100 1
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2026
Label revision date
March 16, 2026
Manufacturer
Jiangxi Yudexi Pharmaceutical Co. , LTD
Registration number
M028
NDC root
85248-161

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Drug Overview

You can use this medication to help remove common warts, which are easily identified by their rough, 'cauliflower-like' appearance. This treatment is specifically designed to target these types of warts, providing a solution for those looking to eliminate them. If you're dealing with common warts, this drug may be a helpful option for you.

Uses

You can use this medication to help remove common warts, which are easily identified by their rough, 'cauliflower-like' surface. This treatment is specifically designed for this purpose, making it a straightforward option for dealing with these skin growths.

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. This makes it a safe choice for those looking to address common warts without additional concerns.

Dosage and Administration

To start treating your wart, first wash the affected area by soaking it in warm water for about 5 minutes. After soaking, make sure to dry the area thoroughly to ensure the medicated plaster sticks properly.

Next, take the medicated patch and remove the bandage strips by peeling off the backing. If the patch is too large for your wart, you can cut it to fit. Carefully apply the medicated plaster directly onto the wart. You should repeat this process every 48 hours as needed, continuing until the wart is removed, but not exceeding a total of 12 weeks.

What to Avoid

It's important to use this medication safely. You should not use it on any irritated, infected, or reddened skin. Additionally, avoid applying it to genital warts, warts on the face, moles, birthmarks, or warts that have hair growing from them. Also, steer clear of using it on mucous membranes, which are the moist tissues lining certain body parts. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

It's important to note that this product is for external use only. If you have diabetes or poor blood circulation, you should consult with your doctor before using it. This precaution helps ensure your safety and the effectiveness of the treatment. If you experience any unusual reactions while using the product, please stop use and seek medical advice.

Warnings and Precautions

This product is intended for external use only, so please avoid swallowing it. If you accidentally ingest it, seek medical help or contact a Poison Control Center immediately.

Before using this product, it's important to consult with your doctor if you have diabetes or experience poor blood circulation, as these conditions may affect how the product works for you. Always prioritize your health and safety by following these guidelines.

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

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 this medication during pregnancy. This means that there are no specific guidelines, dosage adjustments, or precautions outlined for pregnant individuals.

Given this lack of information, you should consult with your healthcare provider before using this medication. They can help you weigh the potential risks and benefits based on your individual circumstances. Always prioritize open communication with your doctor regarding any medications you may be 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. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications 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 a Poison Control Center. Taking quick action can be crucial in ensuring their safety. Always supervise the use of medications around children 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 for personalized advice. 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. This means that there are no tailored recommendations for how your kidney condition might affect the use of this medication.

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

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 are 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 in a cool, dry place at a temperature between 59°F and 86°F (15°C and 30°C). This temperature range helps maintain the integrity and effectiveness of the device.

When handling the product, be sure to do so with clean hands and in a sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safety and compliance with local regulations.

Additional Information

You will apply this treatment topically, meaning you will apply it directly to the skin. You can repeat the application every 48 hours as needed until the wart is removed, but do not use it for more than 12 weeks. If you have any questions about the treatment process or how to use it effectively, be sure to consult with your healthcare provider.

FAQ

What is the drug used for?

The drug is used for the removal of common warts, which are easily recognized by their rough 'cauliflower-like' appearance.

How should I prepare the wart area before applying the medication?

You should wash the affected area and may soak the wart in warm water for 5 minutes, then dry the area thoroughly.

How do I apply the medicated patch?

Remove the bandage strips by peeling the backing off, and if necessary, cut the medicated patch to fit the wart before carefully applying it.

How often should I repeat the application?

You should repeat the procedure every 48 hours as needed until the wart is removed, for up to 12 weeks.

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

Do not use it on irritated, infected, or reddened skin; genital warts; warts on the face; moles; birthmarks; warts with hair; or mucous membranes.

What should I do if I have diabetes or poor blood circulation?

You should ask a doctor before using this medication if you have diabetes or poor blood circulation.

What should I do if the medication is swallowed?

If swallowed, get medical help or contact a Poison Control Center right away.

What are the storage conditions for this medication?

Store the medication between 59° and 86°F (15° and 30°C).

Is there any information regarding use during pregnancy or nursing?

There are no specific warnings or recommendations regarding use during pregnancy or for nursing mothers.

Is this medication safe for children?

Keep this medication out of reach of children, and if swallowed, seek medical help immediately.

Packaging Info

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

Packaging configurations for Odicut Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Odicut 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, which are characterized by their rough, 'cauliflower-like' surface appearance.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The affected area should be washed, and it is recommended to soak the wart in warm water for approximately 5 minutes. After soaking, the area must be dried thoroughly to ensure proper adhesion of the medicated plaster.

To apply the medicated plaster, healthcare professionals should first remove the bandage strips by peeling the backing off. If necessary, the medicated patch may be cut to fit the size of the wart. The plaster should then be carefully applied to the wart.

This procedure may be repeated every 48 hours as needed, continuing until the wart is removed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use is contraindicated on irritated, infected, or reddened skin due to the potential for exacerbation of the condition. Application is also contraindicated on genital warts and warts located on the face, as well as on moles, birthmarks, and warts with hair growing from them, to prevent adverse reactions. Additionally, the product should not be applied to mucous membranes, as this may lead to irritation or other complications.

Warnings and Precautions

For external use only. In the event of accidental ingestion, it is imperative to seek medical assistance or contact a Poison Control Center immediately.

Healthcare professionals should advise patients to consult a physician prior to use if they have a history of diabetes or experience poor blood circulation. This precaution is essential to ensure the safe application of the product and to mitigate any potential risks associated with its use in these populations.

Side Effects

For external use only. Patients are advised to stop use and consult a doctor if they have diabetes or poor blood circulation prior to using the product. It is important for individuals with these conditions to seek medical advice to ensure safe usage.

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

Packaging configurations for Odicut 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 contact with a Poison Control Center is recommended.

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 no information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients and weigh the potential risks and benefits. Women of childbearing potential should be counseled accordingly.

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 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 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 a Poison Control Center if the medication is swallowed. It is crucial for patients to understand the importance of prompt action in such situations.

Additionally, healthcare providers should recommend that patients consult with their doctor prior to using the medication if they have a history of diabetes or poor blood circulation. This precaution is essential to ensure the safe and effective use of the medication in these specific health conditions.

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 within a temperature range of 59° to 86°F (15° to 30°C) to maintain its efficacy and stability. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable container that protects it from environmental factors. Special handling requirements should be observed to prevent any compromise to the product's integrity.

Additional Clinical Information

The medication is administered topically, with the procedure to be repeated every 48 hours 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 Odicut 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 Odicut 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.