ADD CONDITION

items per page

Elsophie Wart Cream

Last content change checked dailysee data sync status

Active ingredient
Salicylic Acid 17 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2026
Label revision date
March 13, 2026
Active ingredient
Salicylic Acid 17 g/100 g
Other brand names
Dosage form
Cream
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 13, 2026
Manufacturer
Shenzhen Xinxin Yunhai Technology Co. , Ltd.
Registration number
M028
NDC root
83818-030

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

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

Drug Overview

You may be looking for a treatment to help with common warts and plantar warts. This medication is specifically designed for the removal of these types of warts, which can be bothersome and sometimes painful. While the exact mechanism of action isn't detailed, its primary purpose is to assist you in getting rid of these skin growths effectively.

If you're dealing with warts, this treatment could be a helpful option to consider for restoring the smoothness of your skin. Always consult with a healthcare professional for personalized advice and to ensure it's the right choice for you.

Uses

You can use this medication to help remove common warts and plantar warts. Common warts are typically found on the hands and fingers, while plantar warts occur on the soles of your feet. This treatment is specifically designed to target these types of warts effectively.

It's important to note that there are no reported teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this medication. This makes it a safe option for those looking to address these skin concerns.

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 the provided applicator to apply one drop of the treatment directly onto each wart, ensuring that it is sufficiently covered. Allow the area to dry after application. You should repeat this process once or twice a day as needed, continuing until the wart is removed, but not exceeding a total of 12 weeks for treatment.

What to Avoid

You should avoid using this product if you have any irritated skin or areas that are infected or reddened. It is also important not to use it if you are diabetic or have poor blood circulation. Additionally, do not apply it to moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes. Following these guidelines will help ensure your safety and well-being.

Side Effects

When using this product, it's important to be aware of potential side effects. You should stop using it if you experience persistent discomfort, severe irritation, or if the wart does not show improvement within 12 weeks. These reactions can indicate that the treatment may not be suitable for you.

If you notice any of these issues, it's a good idea to consult your doctor for further advice. Remember, this product is for external use only, so ensure you follow the guidelines for safe application.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any areas that are irritated, infected, or reddened. If you have diabetes or poor blood circulation, or if you have moles, birthmarks, warts with hair, genital warts, or warts on your face or mucous membranes, do not use this product.

If you accidentally swallow the product, seek medical help or contact a Poison Control Center immediately. You should also stop using the product and call your doctor if you experience persistent discomfort, if irritation becomes severe, or if the wart does not show improvement within 12 weeks.

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 it comes to medications, it's better to be safe and get help if you have any concerns.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no information available about the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions related to pregnancy have not been addressed.

Before taking this medication, you should discuss it with your healthcare provider to understand any potential risks and to ensure the best care for you and your baby. Always prioritize open communication with your doctor regarding any medications you may be considering during 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 use of this medication during nursing. This means that the effects on breast milk production and the nursing infant are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding to ensure the safety and well-being of both you and your baby.

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 a Poison Control Center for guidance. 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 considering this medication, it’s important to consult with a healthcare provider. They can help determine the best approach based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so discussing any concerns with a doctor is essential for ensuring safety and effectiveness.

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 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 might be 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 at room temperature, ideally between 20° and 25°C (68° and 77°F). It's important to keep the container tightly closed when not in use to protect the contents from contamination and maintain their effectiveness.

When handling the product, always do so with clean hands and in a clean environment to avoid introducing any harmful substances. Following these simple storage and handling guidelines will help ensure your product remains safe and effective for use.

Additional Information

You will apply this treatment topically, which means you will apply it directly to the affected area on your skin. You should repeat this procedure once or twice daily as needed, continuing until the wart is removed, but not exceeding a total of 12 weeks. If you have any questions about how to use the treatment or its effects, 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.

How should I apply the drug?

Wash the affected area, soak the wart in warm water for 5 minutes, dry it thoroughly, and apply one drop at a time with an applicator 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 drug?

Do not use this drug on irritated skin, infected areas, or if you are diabetic or have poor blood circulation. Avoid using it on moles, birthmarks, or genital warts.

What should I do if I experience discomfort or irritation?

If discomfort persists or irritation becomes severe, stop using the drug and consult your doctor.

What should I do if the wart does not improve?

If the wart does not improve within 12 weeks, you should stop using the drug and contact your doctor.

Is this drug safe for external use?

Yes, this drug is for external use only.

What should I do if I accidentally swallow the drug?

If swallowed, seek medical help or contact a Poison Control Center immediately.

How should I store this drug?

Store the drug at room temperature between 20°–25°C (68°–77°F) and keep the container tightly closed.

Packaging Info

Below are the non-prescription pack sizes of Elsophie Wart Cream (wart corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Elsophie Wart Cream.
Details

Drug Information (PDF)

This file contains official product information for Elsophie Wart Cream, 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.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

The affected area should be washed thoroughly prior to treatment. For optimal results, it is recommended to soak the wart in warm water for approximately 5 minutes. After soaking, the area must be dried completely.

The medication should be applied using the provided applicator, with one drop at a time, ensuring that each wart is sufficiently covered. It is important to allow the application to dry completely after each use.

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 used in diabetic patients due to the potential for impaired healing and increased risk of complications. Additionally, individuals with poor blood circulation should avoid use, as this may lead to inadequate treatment response and further complications. The product is also contraindicated for application on moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes, due to the risk of adverse effects and complications in these sensitive areas.

Warnings and Precautions

For external use only. This product is contraindicated for application on irritated skin or any area that is infected or reddened. It is also not recommended for use in individuals with diabetes or those who exhibit poor blood circulation. Caution should be exercised to avoid application on moles, birthmarks, warts with hair growing from them, genital warts, or warts located on the face or mucous membranes.

In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Healthcare professionals should instruct patients to discontinue use and consult a physician if discomfort persists, if irritation becomes severe, or if there is no improvement in the wart condition within 12 weeks.

Side Effects

For external use only. Patients should discontinue use if discomfort persists, irritation becomes severe, or if the wart does not improve within 12 weeks. In such cases, it is advisable for patients to consult a healthcare professional.

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 Elsophie Wart Cream (wart corn remover). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Elsophie Wart Cream.
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 therapeutic response, 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 are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential risks and benefits. Women of childbearing potential should be counseled accordingly.

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. 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 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 in these patients to ensure safety and therapeutic effectiveness.

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 compound in these areas.

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 product is swallowed. It is important to instruct patients not to use the product on irritated skin or any area that appears infected or reddened.

Patients should be informed that the product is contraindicated for individuals with diabetes or those who have poor blood circulation. Additionally, healthcare providers should emphasize that 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.

Patients must be counseled to discontinue use if discomfort persists, if irritation becomes severe, or if the wart does not show improvement within 12 weeks. Providers should also remind patients to avoid contact with the eyes during application and to refrain from applying the product to healthy skin surrounding the wart. It is essential to inform patients that skin irritation may occur with the use of this product.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, specifically within the range of 20° to 25°C (68° to 77°F). Proper storage conditions are essential to ensure the product's efficacy and safety.

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 Elsophie Wart Cream, 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 Elsophie Wart Cream, 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.

Learn more in our Editorial Policy

Last AI update:

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.