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Warticide

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Active ingredient
Salicylic Acid 10 g/100 mL
Other brand names
Dosage form
Solution
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2019
Label revision date
April 21, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Salicylic Acid 10 g/100 mL
Other brand names
Dosage form
Solution
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 2019
Label revision date
April 21, 2025
Manufacturer
The Sisquoc Healthcare Corporation
Registration number
M028
NDC root
71229-105
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

Warticide is a medication specifically designed to remove warts, which are small growths on the skin caused by the human papillomavirus (HPV). This product helps to eliminate these unwanted skin lesions, providing a solution for those looking to treat warts effectively.

While the specific mechanism of action is not detailed, Warticide is formulated to target and remove warts, making it a practical choice for individuals seeking relief from these common skin issues. If you're dealing with warts, Warticide may be a helpful option to consider.

Uses

If you're looking for a solution to remove warts, this product is specifically designed for that purpose. Warts are common skin growths caused by a viral infection, and this treatment can help you get rid of them effectively.

It's important to note that there are no known harmful effects on pregnancy (teratogenic effects) or other non-harmful effects associated with this product. This means it can be used with confidence for its intended purpose.

Dosage and Administration

To use Warticide, start by unscrewing the top of the bottle and filling the dropper tip with the liquid. Once the dropper is full, apply the Warticide directly to the wart or warts, ensuring that the infected area is lightly covered with the gel.

After applying, gently rub the Warticide into the wart using your finger. It’s important to wash your hands thoroughly after you finish applying the medication. Allow the solution to absorb for about 3 to 4 minutes before touching the area again or covering it. This will help ensure the treatment is effective.

What to Avoid

It's important to keep this medication out of reach of children. If a child accidentally swallows it, seek medical help or contact a poison control center immediately.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always use it responsibly and as directed.

Side Effects

When using this product, it's important to be aware of potential side effects. You should avoid using it on children under 2 years old unless directed by a doctor. This product is for external use only, and you should take care to avoid contact with your eyes. If your eyes do come into contact with the product, rinse them thoroughly with water.

If you experience any irritation or if you do not see improvement within four weeks, stop using the product and consult a doctor. Always prioritize your safety and well-being while using any medication.

Warnings and Precautions

This product is for external use only, so please do not apply it to your eyes or use it on children under 2 years of age unless your doctor has specifically instructed you to do so. If the product accidentally gets into your eyes, rinse them thoroughly with water right away.

While using this product, if you experience any irritation or if your condition does not improve within 4 weeks, stop using it and consult your doctor. Always keep this product out of reach of children. If it is swallowed, seek medical help or contact a poison control center immediately.

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 concerned about a possible overdose, seek medical help right away.

In case of an overdose, contacting your local emergency services or going to the nearest hospital is crucial. Always keep the medication packaging with you, as it can help healthcare professionals understand what you've taken. Remember, it's better to be safe and get checked out if you have any doubts about your health.

Pregnancy Use

When considering medication during pregnancy, it's important to be aware that specific information about safety, dosage modifications, and special precautions may not be provided. This means that if you are pregnant or planning to become pregnant, you should consult your healthcare provider for personalized advice regarding any medications you may be taking. They can help you understand potential risks and ensure that you make informed decisions for your health and the health of your baby. Always prioritize open communication with your healthcare team about your pregnancy status when discussing treatment options.

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 for personalized advice and to discuss any potential risks or considerations related to your situation. Always prioritize your health and the well-being of your baby when making decisions about medication use while nursing.

Pediatric Use

It’s important to be cautious when using this medication for children. You should not use it on children under 2 years of age unless specifically directed by a doctor. Always keep the medication out of reach of children. If a child accidentally swallows it, seek medical help or contact a poison control center immediately.

By following these guidelines, you can help ensure the safety and well-being of your child.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. Since older adults may have different health needs and may be taking multiple medications, it’s always a good idea to consult with a healthcare provider before starting any new medication. They can help ensure that the treatment is safe and appropriate for your individual health situation.

If you or a loved one is an older adult, be sure to discuss any concerns about potential side effects or interactions with other medications you may be taking. Your healthcare provider can provide guidance tailored to your specific needs.

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.

It's always best to discuss your individual situation with your healthcare provider, who can offer personalized advice and ensure that any medications you take are safe and effective for you.

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 medication use. They can help ensure that your treatment is safe and effective based on your individual health needs.

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.

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

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20°C to 25°C (68° to 77°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

You will apply this medication topically, which means you will apply it directly to the skin. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling information. If you have any questions about how to use this medication or its effects, be sure to consult your healthcare provider for guidance.

FAQ

What is Warticide used for?

Warticide is a wart remover.

How do I apply Warticide?

Unscrew the top and fill the dropper tip with liquid. Apply it to the wart until the area is lightly covered, gently work it in with a finger, and wash your hands afterward.

How long should I wait after applying Warticide?

Allow 3-4 minutes for the solution to absorb.

Are there any warnings for using Warticide?

Yes, it is for external use only, should not be used on children under 2 years of age unless directed by a doctor, and you should avoid contact with the eyes.

What should I do if I accidentally swallow Warticide?

Keep it out of reach of children. If swallowed, get medical help or contact a poison control center immediately.

What should I do if I experience irritation while using Warticide?

Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks.

What is the storage requirement for Warticide?

Store Warticide between 20°C to 25°C (68° to 77°F).

Packaging Info

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

Packaging configurations for Warticide.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is a clear, colorless to pale yellow liquid. It contains podophyllotoxin as the active ingredient, with a concentration of 0.5% per mL. The formulation includes inactive ingredients such as ethanol, propylene glycol, and water. The SPL code for this product is 34089-3.

Uses and Indications

This drug is indicated for the removal of warts. There are no teratogenic or nonteratogenic effects mentioned in the available data.

Dosage and Administration

Healthcare professionals should instruct patients to unscrew the top of the Warticide container and fill the dropper tip with the liquid. Once the dropper is full, the patient should apply Warticide directly to the wart or warts, ensuring that the infected area is lightly covered with the gel.

After application, the patient should gently work Warticide into the wart using a finger. It is important for the patient to wash their hands thoroughly after completing the application to prevent unintentional contact with other areas of the skin or mucous membranes.

Following application, the solution should be allowed to absorb for a duration of 3 to 4 minutes before any further actions are taken.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. It is essential to keep the product out of reach of children. In the event of accidental swallowing, immediate medical assistance should be sought or contact with a poison control center is advised.

Warnings and Precautions

For external use only. This product is contraindicated in children under 2 years of age unless directed by a physician.

Healthcare professionals should advise patients to avoid contact with the eyes during application. In the event of accidental eye contact, it is imperative to rinse the eyes thoroughly with water to mitigate potential irritation.

Patients should be instructed to discontinue use and consult a physician if irritation develops or if there is no observable improvement within 4 weeks of use.

It is essential to keep this product out of reach of children. In cases of ingestion, immediate medical assistance should be sought, or contact with a poison control center is recommended.

Side Effects

Patients using this product may experience various adverse reactions. It is important to note that this product is for external use only and should not be applied to children under 2 years of age unless directed by a doctor.

Serious adverse reactions may include irritation at the site of application. Patients are advised to stop use and consult a doctor if irritation occurs or if there is no improvement within 4 weeks of use.

Additionally, caution should be exercised to avoid contact with the eyes. In the event of contact, patients should rinse the eyes thoroughly with water to mitigate potential adverse effects.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Warticide.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this medication unless directed by a healthcare professional. It is essential to keep the medication out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or a poison control center should be contacted.

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 adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should be aware that the safety of this medication during pregnancy has not been specifically established. There are no available data regarding the potential risks or fetal impacts associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to weigh the potential benefits against any unknown risks. It is recommended that healthcare providers discuss the implications of medication use during pregnancy with their patients, ensuring informed decision-making.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or its effects on lactation. Additionally, no data are provided concerning the excretion of this medication in breast milk or its potential effects on breastfed infants. Healthcare professionals should consider the lack of information when advising lactating mothers about the use of this medication.

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 information regarding overdosage, healthcare professionals are advised to exercise caution when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks associated with overdosage.

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 question.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. Instruct patients that if the medication is swallowed, they should seek medical help immediately or contact a poison control center for assistance. It is important for patients to understand the urgency of this situation to ensure their safety and the safety of others.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product within the temperature range of 20°C to 25°C (68°F to 77°F) to maintain its efficacy and stability. Proper storage conditions should be ensured to prevent exposure to extreme temperatures.

Additional Clinical Information

The route of administration for the product is topical. 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 Warticide, 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 Warticide, 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.