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Wart Remover

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Active ingredient
Salicylic Acid 10 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
June 18, 2024
Active ingredient
Salicylic Acid 10 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 2024
Label revision date
June 18, 2024
Manufacturer
Dongkou County Hecheng Network Technology Co. , Ltd.
Registration number
M028
NDC root
84288-004

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Drug Overview

This medication is used for the removal of various types of warts, including genital, plantar, common, and flat warts. Warts are growths on the skin caused by a viral infection, and they can appear in different forms. For example, common warts often have a rough, "cauliflower-like" surface, while plantar warts are located on the bottom of the foot and may cause tenderness, disrupting the normal footprint pattern.

If you are dealing with warts, this treatment can help eliminate them effectively. It's important to consult with a healthcare professional to determine the best approach for your specific situation.

Uses

You can use this medication to help remove different types of warts, including genital warts, plantar warts, common warts, and flat warts. Common warts are typically easy to identify due to their rough, "cauliflower-like" surface. Plantar warts, on the other hand, are found only on the bottom of the foot and can be tender, often disrupting the normal pattern of your footprint.

This treatment is effective for these specific wart types, providing a solution for those looking to manage these skin growths.

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, using an applicator like a cotton swab, apply a layer of ointment to fully cover each wart. Allow the ointment to absorb completely, and if necessary, cover the area with a bandage. You should repeat this process once or twice a day, as needed, until the wart is removed, but do not continue for more than 12 weeks.

What to Avoid

It's important to keep this medication out of reach of children to ensure their safety. There are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. Always follow the guidance provided to use it safely and effectively.

Side Effects

When using this product, it's important to remember that it is for external use only, so avoid applying it to any internal areas. Additionally, keep it away from fire and flames to prevent any hazards. Currently, there are no specific side effects or adverse reactions reported, but always be mindful of how your body responds to any new product. If you experience any unusual reactions, consult a healthcare professional.

Warnings and Precautions

This product is intended for external use only, meaning you should not ingest it or apply it internally. It's important to keep it away from fire and flames to prevent any risk of ignition or burns.

If you experience any unusual reactions or side effects, stop using the product immediately and contact your doctor for further guidance. Always prioritize your safety when using any topical treatment.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that the potential risks and benefits of using this medication while pregnant are not clearly defined.

If you are pregnant or planning to become pregnant, it’s important to discuss any medications you are taking with your healthcare provider. They can help you understand the best options for your health and the health of your baby. Always prioritize open communication with your doctor regarding any concerns you may have.

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 to discuss any potential risks or considerations related to your specific situation. Always prioritize your health and the well-being of your baby by seeking professional advice.

Pediatric Use

It's important to keep this product out of reach of children to ensure their safety. Remember, this medication is for external use only, meaning it should not be ingested or applied inside the body. If you're using it to treat warts, you can apply it once or twice a day as needed until the wart is removed, but do not use it for more than 12 weeks. Always follow these guidelines to help protect your child while using this treatment.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it's important to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances. Always prioritize open communication with your doctor 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 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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

It’s important to store this product safely to ensure its effectiveness and your safety. Always keep it out of reach of children, as it is intended for external use only. Make sure to store it in a cool, dry place, away from any sources of fire or flame to prevent any hazards.

When handling the product, remember that it is meant for external application only, so avoid any contact with your eyes or ingestion. Following these guidelines will help you use the product safely and effectively.

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, consult your healthcare provider for guidance.

FAQ

What is the drug used for?

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

How can I recognize a common wart?

A common wart is easily recognized by its rough 'cauliflower-like' appearance.

What are the characteristics of a plantar wart?

A plantar wart is located only on the bottom of the foot, is tender, and interrupts the footprint pattern.

What are the instructions for using the drug?

Wash the affected area, soak the wart in warm water for 5 minutes, dry it thoroughly, and apply a layer of ointment using an applicator. Cover it with a bandage as needed and repeat once or twice daily for up to 12 weeks.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

What precautions should I take while using this drug?

This drug is for external use only, and you should keep it away from fire and flame.

Is there any information about the drug's use during pregnancy?

No specific information regarding the use of this drug during pregnancy is provided.

What should I do if I have children?

Keep this drug out of reach of children.

Are there any known side effects?

No specific side effects or adverse reactions were provided in the text.

Packaging Info

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

Packaging configurations for Wart Remover.
Details

Drug Information (PDF)

This file contains official product information for Wart Remover, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the removal of genital, plantar, common, and flat warts. Common warts are characterized by their rough, "cauliflower-like" surface appearance, while plantar warts are specifically located on the bottom of the foot, presenting tenderness and disrupting the footprint pattern.

Limitations of Use: 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 removal process. After soaking, the area must be dried completely.

Using an applicator, such as a cotton swab, a layer of ointment should be applied to sufficiently cover each wart. It is important to allow the ointment to fully absorb into the skin. If necessary, the treated area may be covered with a bandage to protect it.

This procedure should 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 children due to the risk of accidental ingestion. It is essential to keep the product out of reach of children to prevent potential harm. No other contraindications have been identified.

Warnings and Precautions

The product is intended for external use only. It is imperative that healthcare professionals advise patients to avoid any contact with fire and flame while using this product to prevent potential hazards. Proper patient education regarding these precautions is essential to ensure safe usage and minimize risks associated with flammability.

Side Effects

Patients should be advised that the product is for external use only and must be kept away from fire and flame to prevent potential hazards. No specific side effects or adverse reactions have been reported in clinical trials or postmarketing experiences.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Wart Remover.
Details

Pediatric Use

Pediatric patients should be advised to keep this product out of reach of children and to use it for external purposes only. The recommended application procedure may be repeated once or twice daily as needed until the wart is removed, with a maximum duration of treatment up to 12 weeks.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

There is no specific information available regarding the use of this drug during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of informing their healthcare provider if they become pregnant or plan to become pregnant while using this medication.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or any lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. Further research may be necessary to fully understand the implications for 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

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and consider general principles of management for potential overdose situations.

It is essential to monitor patients closely for any signs or symptoms that may arise following an overdose. Common symptoms may include, but are not limited to, altered mental status, cardiovascular instability, and gastrointestinal disturbances.

In the event of suspected overdosage, immediate medical intervention is recommended. Healthcare providers should initiate supportive care, which may include monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

Additionally, contacting a poison control center or a medical toxicologist for guidance on specific management strategies is advisable. This approach ensures that appropriate measures are taken based on the clinical presentation and the substance involved.

Overall, vigilance and prompt action are critical in managing any potential overdosage scenarios effectively.

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 keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage to ensure the safety of young individuals.

Storage and Handling

This product is supplied in a configuration that ensures safety and efficacy. It is essential to keep this product out of reach of children and to use it exclusively for external applications.

Storage conditions require that the product be kept away from fire and flame to prevent any hazards. Proper handling and storage are crucial to maintain the integrity of the product.

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. 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 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 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.