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Skin Tag Remover

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Active ingredient
Salicylic Acid 15 mg/1 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
November 14, 2025
Active ingredient
Salicylic Acid 15 mg/1 g
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 2025
Label revision date
November 14, 2025
Manufacturer
Guangzhou ChuanMa International Trading Co. , Ltd.
Registration number
M028
NDC root
85593-120

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Drug Overview

This medication comes in the form of a patch that you apply directly over a wart or skin tag. It is designed to help remove these growths by being placed on the affected area, which should be washed thoroughly before application. You will need to replace the patch every 48 hours as needed, and you can continue this process for up to 12 weeks until the wart or tag is removed.

Uses

If you have a wart or skin tag that you want to remove, you can follow a simple process. Start by washing the affected area thoroughly to ensure it's clean. Then, apply the patch directly over the wart or skin tag. You should repeat this procedure every 48 hours as needed until the wart or tag is completely removed, which can take up to 12 weeks.

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 treatment. This makes it a safe option for many individuals looking to address these skin concerns.

Dosage and Administration

To treat your wart or skin tag, start by applying the patch directly over the affected area. It's important to ensure that the patch is placed correctly for the best results. You should repeat this application every 48 hours, which means you’ll put on a new patch every two days. Continue this process until the wart or tag is completely removed, but do not exceed a total treatment time of 12 weeks. This method is designed to help you effectively manage the condition while keeping your skin healthy.

What to Avoid

It's important to keep this product out of reach of children to ensure their safety. If a child accidentally swallows it, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this product. However, always use it responsibly and follow the instructions provided.

Side Effects

It's important to note that this product is for external use only. This means you should not apply it to your eyes, mouth, or any internal areas. Always follow the instructions for use to ensure your safety and well-being. If you have any concerns or experience unusual reactions, consult a healthcare professional.

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to any areas that are not meant for topical treatment. It's important to keep this product out of reach of children. If a child accidentally swallows it, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

Always use this product as directed, and if you have any concerns or experience unusual reactions, stop using it and consult your doctor for further guidance. Your safety is a priority, so please take these precautions seriously.

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 attention.

In case of an emergency, call your local emergency services 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

When it comes to using this medication during pregnancy, there is currently no information available about its safety, recommended dosage adjustments, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it is essential to consult with your healthcare provider before starting or continuing this medication. They can help you understand any potential risks and make informed decisions about your treatment options. Always prioritize your health and the health of your baby by seeking professional guidance.

Lactation Use

If you are breastfeeding and considering using the skin tag remover that contains salicylic acid, it's important to note that there is no specific information available about its effects on nursing mothers or lactation (the process of producing milk). Since the drug insert does not address this topic, it’s advisable to consult your healthcare provider for personalized guidance. They can help you weigh the potential risks and benefits based on your individual situation.

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 at 1-800-222-1222.

Remember, this medication is intended for external use only, so it should not be applied to the inside of the mouth or any other internal areas. Always supervise its use to ensure safety.

Geriatric Use

While there is no specific information about how this medication should be used by older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions that may be present.

Remember, even if there are no specific dosage adjustments or safety concerns mentioned, your healthcare provider may still recommend monitoring for any potential side effects or interactions with other medications you may be taking. Always prioritize open communication with your healthcare team to ensure the best care.

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 plan.

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 if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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 known interactions between this medication and other drugs or laboratory tests. However, your healthcare provider can help ensure that your treatment plan is safe and effective, taking into account your unique health situation. Always feel free to ask questions or express any concerns you may have regarding your medications or tests.

Storage and Handling

It's important to keep this product out of reach of children to ensure their safety. Remember, this product is for external use only, meaning it should not be ingested or applied internally. After you open the product, please discard it to maintain safety and effectiveness.

When handling the product, always ensure that you are in a clean environment to avoid contamination. Following these guidelines will help you use the product safely and effectively.

Additional Information

You will apply the patch directly over the wart or skin tag, using it topically. Repeat this application every 48 hours as needed, continuing until the wart or tag is removed, which may take up to 12 weeks. If you have any questions about the process or need further assistance, consult your healthcare provider.

FAQ

How do I use the patch?

Wash the affected area thoroughly, dry it completely, and apply the patch directly over the wart or tag. Repeat this every 48 hours as needed until the wart or tag is removed, for up to 12 weeks.

What should I do if the patch is swallowed?

Keep the patch out of reach of children. If swallowed, get medical help or contact a Poison Control Center at 1-800-222-1222 right away.

Are there any contraindications for using this patch?

No contraindications are listed for this patch.

Is this patch safe for external use?

Yes, the patch is for external use only.

What should I do if I experience any issues while using the patch?

If you experience any problems, consult a healthcare professional for advice.

Is there any information about using this patch during pregnancy or while nursing?

No specific information regarding use during pregnancy or lactation is provided.

How often should I apply the patch?

You should apply the patch every 48 hours as needed until the wart or tag is removed, for up to 12 weeks.

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 description information is available for the specified drug.

Uses and Indications

This drug is indicated for the treatment of warts and skin tags. Patients should wash the affected area thoroughly before application. The patch should be applied directly over the wart or skin tag. This procedure may be repeated every 48 hours as needed until the wart or skin tag is removed, with a maximum treatment duration of up to 12 weeks.

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

Dosage and Administration

The patch should be applied directly over the wart or skin tag. This procedure may be repeated every 48 hours as necessary, continuing until the wart or skin tag is removed, with a maximum treatment duration of up to 12 weeks.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical assistance should be sought or contact with a Poison Control Center (1-800-222-1222) is advised.

Warnings and Precautions

For external use only. It is imperative that this product is kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted at 1-800-222-1222.

Side Effects

For external use only. Patients should be advised to avoid contact with eyes and mucous membranes. In the event of accidental contact, patients should rinse thoroughly with water. Adverse reactions associated with the use of this product have not been specifically detailed in clinical trials or postmarketing experiences. Therefore, healthcare providers should monitor patients for any unexpected reactions and report them as necessary.

Drug Interactions

There are currently no documented drug interactions associated with the use of 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 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 product 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.

This product is intended for external use only and should not be applied to children in any manner that could lead to ingestion or inappropriate exposure.

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

There is no information available regarding the use of this drug 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 on the absence of information related to pregnancy and advised to discuss any concerns with their healthcare provider.

Lactation

There is no information available regarding the use of the SKIN TAG REMOVER (salicylic acid patch) in lactating mothers or its effects on breastfed infants. Healthcare professionals should consider this lack of data when advising lactating patients.

Renal Impairment

There is no specific information available 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 overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, altered mental status, cardiovascular instability, or gastrointestinal disturbances.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. Healthcare professionals should also consider contacting a poison control center for additional guidance on the management of overdose cases.

It is crucial to document any instances of overdose and report them to the appropriate regulatory authorities to enhance the understanding of the medication's safety profile.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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. It is important to inform patients that if the medication is swallowed, they should seek medical help immediately or contact a Poison Control Center at 1-800-222-1222. This precaution is essential to ensure the safety and well-being of children who may inadvertently access the medication.

Storage and Handling

The product is supplied in a configuration that ensures safety and efficacy for external use only. It is imperative to keep the product out of reach of children to prevent accidental ingestion or misuse.

Upon opening, the product should be discarded to maintain safety and integrity. Proper handling and storage conditions are essential to ensure the product remains effective and safe for use.

Additional Clinical Information

The product is administered topically, with the patch applied directly over the wart or tag. This procedure may be repeated every 48 hours as necessary, continuing for up to 12 weeks until the wart or tag is removed. No additional information is available regarding laboratory tests, abuse potential, 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.