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Dr. Miraculous Wart Remover Liquid

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Active ingredient
Salicylic Acid 5 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
May 9, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Salicylic Acid 5 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2025
Label revision date
May 9, 2025
Manufacturer
Shenzhen Zealous Ecommerce Technology Co. , Ltd
Registration number
M028
NDC root
85587-003
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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

This medication is designed to help you remove common warts, which are rough, raised growths that often appear on your hands, fingers, or knees. It is also effective for treating plantar warts, which are hard, flat lesions found on the soles of your feet and can be tender, sometimes surrounded by thickened skin. If you're dealing with these types of warts, this treatment may provide the relief you need.

Uses

You can use this medication to effectively remove common warts and plantar warts. Common warts are rough, raised growths that often appear on your hands, fingers, or knees and have a texture similar to cauliflower. Plantar warts, on the other hand, are hard, flat lesions that develop on the soles of your feet and can be quite tender, often surrounded by thickened skin.

This treatment is designed to target these specific types of warts, helping you achieve smoother skin without the worry of any teratogenic effects (which means it won't cause birth defects).

Dosage and Administration

To treat your wart, start by using the applicator tip to place 1 to 2 drops of the medication directly onto the wart, ensuring it is fully covered. After applying the drops, allow the area to dry completely. For the best results, repeat this process 1 to 2 times each day. Consistency is key, so try to stick to this routine for effective treatment.

What to Avoid

It's important to be cautious when considering this medication. You should not use it if you have diabetes, peripheral artery disease, or poor circulation, as these conditions can lead to serious complications. Additionally, avoid applying the medication to irritated, infected, broken, or sunburned skin. It’s also crucial not to use it on moles, birthmarks, facial or genital warts, or warts that have hair.

By following these guidelines, you can help ensure your safety and the effectiveness of the treatment. If you have any questions or concerns about your health conditions or how to use this medication, please consult your healthcare provider.

Side Effects

You may experience some side effects when using this product. Common reactions include temporary skin irritation, redness, peeling, and changes in skin color, such as darkening or lightening at the application site.

It's important to note that this product is flammable, so keep it away from flames, sparks, or heat sources, and use it only on the skin—avoid contact with your eyes, mouth, or mucous membranes. If you have any concerns about these side effects, please consult your doctor.

Warnings and Precautions

It's important to use this product safely. Remember that it is flammable, so keep it away from flames, sparks, and heat sources. This product is for external use only, and you should avoid applying it to your eyes, mouth, or any mucous membranes.

Before using, ensure you do not apply it to irritated, infected, broken, or sunburned skin. It's also best to avoid using it on moles, birthmarks, facial or genital warts, or warts with hair. If you have diabetes, peripheral artery disease, or poor circulation, you should not use this product.

If you notice that the wart and the surrounding dead tissue have detached, or if you reach the maximum treatment duration of 12 weeks, stop using the product and call your doctor for further guidance.

Overdose

If you suspect an overdose, it's important to be aware that there is no specific information available about the effects of taking too much of this medication. However, if you experience unusual symptoms or feel unwell after taking the medication, you should seek medical help immediately.

Signs of an overdose can vary, but they may include severe drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, or if you are unsure about your situation, do not hesitate to contact a healthcare professional or call emergency services for assistance. Your safety is the top priority, so it's always better to err on the side of caution.

Pregnancy Use

The safety of this product during pregnancy has not been established, so it's important to approach its use with caution. There is no specific information available about potential risks to a developing fetus, which means the effects are unknown. If you are pregnant or planning to become pregnant, it is crucial to consult your healthcare provider before using this product to ensure it is safe for you and your baby.

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 and your baby are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding. They can help you weigh the potential risks and benefits to ensure the safety of both you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children to ensure their safety. If your child has diabetes, peripheral artery disease, or poor circulation, you should not use this medication, as it may not be safe for them. Always consult with a healthcare professional if you have any concerns about its use in children or if you need guidance on appropriate alternatives.

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 and benefits with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances.

Renal Impairment

It appears that there is no specific information regarding dosage adjustments, monitoring, or safety considerations for patients with kidney problems in the provided drug insert. This means that if you have renal impairment (kidney issues), you should consult your healthcare provider for personalized advice and guidance regarding your treatment. They can help determine the best approach for your situation, ensuring your safety and the effectiveness of your medication. Always keep your doctor informed about your kidney health when discussing any 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 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 important to communicate openly with your healthcare provider about any medications you are taking. In this case, there are no reported interactions between this medication and other drugs or laboratory tests. This means that, as far as current knowledge goes, you can use this medication without worrying about it affecting other treatments or test results.

However, always keep in mind that individual responses can vary. Discussing your full list of medications and any upcoming lab tests with your healthcare provider ensures that you receive the safest and most effective care tailored to your needs.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature, away from any flames, sparks, or heat sources. This helps maintain its integrity and prevents any potential hazards.

Additionally, it's important to keep the product out of reach of children to avoid any accidental misuse. By following these simple storage and handling guidelines, you can help ensure a safe experience with your device.

Additional Information

You will apply this treatment topically, which means you will apply it directly to the skin. To use it, place 1–2 drops onto the wart using the applicator tip until the wart is fully covered. Allow it to dry, and repeat this process 1–2 times daily for the best results.

FAQ

What types of warts does this drug remove?

This drug removes common warts, which are rough, raised growths with a 'cauliflower-like' texture, and plantar warts, which are hard, flat lesions on the soles of the feet.

How do I use this drug?

Using the applicator tip, place 1–2 drops directly onto the wart until fully covered, let it dry, and use 1–2 times daily.

What precautions should I take when using this drug?

Avoid using it on irritated, infected, broken, or sunburned skin, as well as on moles, birthmarks, facial/genital warts, or warts with hair.

Are there any contraindications for using this drug?

Do not use this drug if you have diabetes, peripheral artery disease, or poor circulation.

What are the possible side effects?

Possible side effects include temporary skin irritation, redness, peeling, darkening, or lightening of the skin at the application site.

Is this drug safe to use during pregnancy?

The safety of this product during pregnancy has not been established, so consult a healthcare provider before use if you are pregnant or planning to become pregnant.

What should I do if I experience side effects?

Discontinue use once the wart and surrounding dead tissue detach or after the maximum treatment duration of 12 weeks, and consult your doctor if side effects persist.

How should I store this drug?

Store at room temperature, away from flames, sparks, or heat sources, and keep out of reach of children.

Packaging Info

Below are the non-prescription pack sizes of Dr. Miraculous Wart Remover Liquid (wart remover liquid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr. Miraculous Wart Remover Liquid.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available data.

Uses and Indications

This drug is indicated for the removal of common warts and plantar warts.

Common warts are characterized as rough, raised growths with a "cauliflower-like" texture, typically found on the hands, fingers, or knees. Plantar warts are identified as hard, flat lesions located on the soles of the feet, which are often tender and may be surrounded by thickened skin.

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

Dosage and Administration

Using the applicator tip, healthcare professionals should apply 1 to 2 drops directly onto the wart, ensuring that the wart is fully covered. After application, it is important to allow the solution to dry completely. This treatment may be administered 1 to 2 times daily, depending on the clinical judgment of the healthcare provider and the specific needs of the patient.

Contraindications

Use is contraindicated in patients with diabetes, peripheral artery disease, or poor circulation due to the increased risk of complications associated with these conditions.

Additionally, the product should not be applied to irritated, infected, broken, or sunburned skin, as well as to moles, birthmarks, facial or genital warts, or warts with hair, to prevent adverse reactions and ensure safety.

Warnings and Precautions

The use of this product necessitates adherence to specific warnings and precautions to ensure patient safety and efficacy.

Safety Precautions This product is flammable; therefore, it must be kept away from flames, sparks, or heat sources. It is intended for external use only and should not be applied to the eyes, mouth, or mucous membranes.

General Precautions The product should not be used on irritated, infected, broken, or sunburned skin. Additionally, it is contraindicated for application on moles, birthmarks, facial or genital warts, or warts that have hair. Patients with diabetes, peripheral artery disease, or poor circulation should avoid using this product due to the increased risk of complications.

Discontinuation Instructions Patients are advised to discontinue use of the product once the wart and surrounding dead tissue have detached or upon reaching the maximum treatment duration of 12 weeks. In such cases, it is essential to consult a healthcare professional for further guidance.

Side Effects

Patients using this product may experience a range of adverse reactions, which can be categorized into common side effects.

Common adverse reactions reported include temporary skin irritation, redness at the application site, peeling at the application site, darkening of the skin, and lightening of the skin. These reactions are generally mild and may resolve with continued use or upon discontinuation of the product.

It is important to note that the product is flammable; therefore, patients should keep it away from flames, sparks, or heat sources. The product is intended for external use only and should not be applied to the eyes, mouth, or mucous membranes.

Patients are advised to consult their healthcare provider if they experience any of these side effects or have concerns regarding their use of the product.

Drug Interactions

There are currently 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 or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Dr. Miraculous Wart Remover Liquid (wart remover liquid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr. Miraculous Wart Remover Liquid.
Details

Pediatric Use

Pediatric patients should be advised to keep the medication out of reach of children. The use of this medication is contraindicated in individuals with diabetes, peripheral artery disease, or poor circulation. Caution is advised when considering treatment options for pediatric patients with these conditions.

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. Caution is advised as the effects on a developing fetus are unknown. There is no specific information available regarding risks to the fetus. No dosage modifications for pregnant individuals are mentioned. It is recommended that pregnant patients or those planning to become pregnant consult a healthcare provider before use.

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

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

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 based on clinical judgment.

Overdosage

In the absence of specific information regarding overdosage in the provided sections of the Summary of Product Characteristics (SPL), healthcare professionals are advised to exercise caution and consider general principles of management in cases of suspected overdosage.

Recommended Actions In the event of an overdosage, it is essential for healthcare providers to assess the patient's clinical status and initiate appropriate supportive care. Monitoring of vital signs and symptomatic treatment should be prioritized.

Potential Symptoms While specific symptoms of overdosage are not detailed, healthcare professionals should remain vigilant for any unusual or severe reactions that may arise, given the pharmacological profile of the medication.

Management Procedures In the absence of specific antidotes or treatment protocols, healthcare professionals should refer to established guidelines for the management of overdosage related to similar pharmacological agents. Consultation with a poison control center may also be beneficial in guiding the management of the patient.

Overall, due diligence in monitoring and supportive care is paramount in managing any suspected overdosage cases 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 use of the compound in these contexts.

Postmarketing Experience

Postmarketing experience has identified several adverse events reported voluntarily or through surveillance programs. Users have noted the occurrence of temporary skin irritation, redness, or peeling at the application site. Additionally, changes in skin pigmentation, including darkening or lightening, have been observed. It is advised that individuals consult a healthcare professional if these effects persist.

Patient Counseling

Healthcare providers should advise patients to consult a doctor if they experience persistent side effects following the use of the medication. It is important to inform patients that possible side effects may include temporary skin irritation, redness, or peeling at the application site. Additionally, patients should be made aware that changes in skin pigmentation, such as darkening or lightening of the skin, may also occur. Encouraging open communication about these potential effects can help ensure patient safety and satisfaction with their treatment.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It should be stored at room temperature, ensuring that it is kept away from flames, sparks, or any heat sources to maintain its integrity. Additionally, it is essential to keep the product out of reach of children to ensure safety during storage and handling.

Additional Clinical Information

The product is administered topically, with the recommended method involving the application of 1–2 drops directly onto the wart until it is fully covered. This should be allowed to dry and can be applied 1–2 times daily. 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 Dr. Miraculous Wart Remover Liquid, 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 Dr. Miraculous Wart Remover Liquid, 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

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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.