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Skin Tag 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
84288-003

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If you are a consumer or patient please visit this version.

Drug Overview

This medication is used to remove various types of warts, including genital warts, plantar warts, common warts, and flat warts. Common warts typically have a rough, "cauliflower-like" surface, while plantar warts are found only on the bottom of the foot and can be tender, disrupting the normal footprint pattern.

If you are dealing with any of these warts, this treatment can help you effectively eliminate them and improve your skin's appearance.

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 their skin condition.

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 as an applicator to apply a layer of ointment that fully covers 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 noted risks of abuse, misuse, or dependence associated with this medication. Always follow the guidance provided by your healthcare professional and use the medication responsibly.

Side Effects

When using this product, it's important to be aware that it is for external use only, so avoid applying it to areas that may come into contact with fire or flames. While specific side effects are not detailed, always monitor your body’s response after use. If you experience any unusual reactions, consult a healthcare professional promptly.

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 there is no specific information available about the signs of overdose for this medication, general 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 always better to be safe and get checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Pregnancy Use

It’s important to be cautious about the use of certain products during pregnancy. The safety of this product has not been established, and it is specifically contraindicated (not recommended) for use during pregnancy due to potential risks to your developing baby. There may be a risk of teratogenic effects, which means it could cause developmental issues in the fetus.

If you are pregnant or planning to become pregnant, you should avoid using this product unless your healthcare provider specifically advises you to do so. Always consult with your doctor for guidance on safe options during your pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the effects of this medication on nursing mothers or lactation (the process of producing breast milk). Since there are no guidelines or data provided, it’s advisable to consult your healthcare provider for personalized advice and to discuss any potential risks or concerns related to your situation. Your healthcare provider can help you make informed decisions that prioritize both your health and your baby's well-being.

Pediatric Use

It's important to keep this medication out of reach of children. This precaution helps prevent accidental ingestion, which can be dangerous. Always store it in a safe place where children cannot access it, ensuring their safety at all times. If you have any concerns or questions about the medication, don't hesitate to reach out to your healthcare provider for guidance.

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 to using this medication safely and effectively, considering any unique health needs or conditions that may be present. Always prioritize open communication with your healthcare team to ensure the best outcomes.

Renal Impairment

If you have kidney problems, 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 usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment and what steps to take for your safety.

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 great to know that there are no reported interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective, tailored specifically to your health needs.

Always keep your healthcare provider informed about any changes in your medication or health status. Open communication helps prevent any potential issues and supports your overall well-being.

Storage and Handling

It's important to store this product safely by keeping it out of reach of children to prevent any accidental use. Remember, this product is for external use only, so avoid applying it to any internal areas. Additionally, ensure that you keep it away from fire and flame to maintain safety during use.

When handling the product, always follow these guidelines to ensure your safety and the effectiveness of the product. By adhering to these simple precautions, you can 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 indicated for?

The drug is indicated 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 of the surface.

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 should I do before applying the ointment?

Wash the affected area, soak the wart in warm water for 5 minutes, and dry the area thoroughly.

How do I apply the ointment?

Using an applicator (cotton swab), apply a layer of ointment to sufficiently cover each wart and allow it to fully absorb.

How often should I repeat the application?

Repeat the procedure once or twice daily as needed until the wart is removed, for up to 12 weeks.

Are there any contraindications for this drug?

No contraindications are listed, but keep the product out of reach of children.

Is this drug safe to use during pregnancy?

The safety of this product during pregnancy has not been established, and its use is contraindicated due to potential risks to the fetus.

What precautions should pregnant women take?

Pregnant women should avoid using this product unless directed by a healthcare provider.

What are the warnings associated with this drug?

This drug is for external use only and should be kept away from fire and flame.

Packaging Info

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

Packaging configurations for Skin Tag Remover.
Details

Drug Information (PDF)

This file contains official product information for Skin Tag 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 warts, plantar warts, common warts, 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.

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 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.

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 is contraindicated in children due to the risk of accidental ingestion. There are no other contraindications listed for this product.

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 during the application and use of this product. Proper precautions should be taken to ensure that the product is stored and used in a safe environment to minimize the risk of fire hazards.

Side Effects

Patients should be aware that the product is intended for external use only. It is crucial to keep the product away from fire and flame to prevent any potential hazards.

No additional adverse reactions have been reported in clinical trials or postmarketing experiences.

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Skin Tag Remover.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. It is essential to ensure that children do not have access to the medication to prevent accidental ingestion or misuse.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

The safety of this product during pregnancy has not been established. The use of salicylic acid is contraindicated in pregnancy due to potential risks to the fetus, including the possibility of teratogenic effects. Pregnant women should avoid using this product unless directed by a healthcare provider. It is essential for healthcare professionals to counsel women of childbearing potential regarding these risks and to consider alternative treatments when necessary.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established.

Renal Impairment

There is no specific information 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 detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in 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 adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of antidotes or specific treatments should be considered based on the substance involved and the clinical presentation. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

Documentation of the incident, including the substance, amount ingested, and time of ingestion, is crucial for effective management and treatment.

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 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

The product is supplied in a configuration that ensures safety and efficacy. It is essential to keep this product out of reach of children to prevent accidental ingestion or misuse. The product is intended for external use only, and users should adhere strictly to this guideline to avoid any adverse effects.

Storage conditions require that the product be kept away from fire and flame to maintain its integrity and safety. Proper handling and storage are crucial to ensure the product remains effective and safe for use.

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 Skin Tag 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 Skin Tag 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.