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Preboost

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Benzocaine 4 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 2014
Label revision date
February 18, 2014
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 4 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 2014
Label revision date
February 18, 2014
Manufacturer
944 Corp
Registration number
part348
NDC root
62192-8500
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

PREBOOST™ is a product designed specifically for men, consisting of desensitizing wipes that help temporarily prolong the time until ejaculation. Developed by Dr. Harry Fisch, these wipes are easy to use and come in a single-use premoistened towelette format, making them convenient for personal use.

If you're looking for a way to enhance your intimate experiences, PREBOOST™ may be a helpful option to consider. For more information, you can visit their website at www.preboost.com.

Uses

This medication is designed to help you temporarily prolong the time until ejaculation, which can be beneficial for those experiencing premature ejaculation. It works by affecting the way your body responds during sexual activity, allowing for a more satisfying experience.

It's important to note that this medication does not have any teratogenic effects, meaning it does not cause harm to a developing fetus. Additionally, there are no reported nonteratogenic effects, which means it does not cause other types of developmental issues. Always consult with your healthcare provider for personalized advice and information.

Dosage and Administration

To use this medication, you should apply a small amount to the head and shaft of your penis before engaging in intercourse. It's important to follow your doctor's instructions if they have provided specific guidance on how to use the product.

After intercourse, make sure to wash the product off thoroughly. This helps ensure that the medication is used safely and effectively. Always remember to follow any additional advice from your healthcare provider regarding its use.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. If you accidentally swallow it, seek medical help or contact a poison control center immediately. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence (a condition where your body becomes reliant on a substance). However, always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

Using this product may lead to some side effects that you should be aware of. If you experience premature ejaculation, it could be a sign of an underlying condition that needs medical attention. If the product does not help, stop using it and talk to your doctor.

Additionally, avoid getting the product in your eyes. If you or your partner notice any rashes or irritation, such as burning or itching, stop using it immediately. Should any symptoms continue, please consult your doctor for further advice.

Warnings and Precautions

If you are experiencing premature ejaculation, it may be a sign of a condition that needs medical attention. If this product does not help you as directed, please stop using it and consult your doctor for further guidance.

Be careful to avoid contact with your eyes, as this can cause irritation. If you or your partner notice any rash, burning, or itching while using the product, stop using it immediately and seek medical advice. If your symptoms continue, it’s important to consult your doctor for further evaluation.

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

Currently, there is no available information about the use of PREBOOST (benzocaine liquid) during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been established. If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product to ensure your safety and the safety of your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding nursing mothers or lactation in the information provided. This means that, based on the available data, there are no known risks associated with breastfeeding while using this medication. However, it's always a good idea to consult with your healthcare provider about any concerns you may have regarding your health and breastfeeding.

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. Taking quick action can be crucial in ensuring their safety. Always be vigilant and store medications securely to prevent any accidents.

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 wise to discuss any potential risks or concerns with your 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 regular check-ins with your doctor can ensure 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 you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use with other drugs and tests. However, every individual is different, and your healthcare provider can help ensure that your treatment plan is safe and effective for you.

Always discuss any changes in your medication or health status with your healthcare provider to avoid any potential issues and to get the best care possible.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. It's important to keep it out of reach of children to prevent any accidental ingestion or misuse. Once you open the product, be sure to discard it after use to maintain safety and hygiene. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should apply a small amount of the product to the head and shaft of the penis before intercourse, or use it as directed by your doctor. After intercourse, make sure to wash the product off. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is PREBOOST™?

PREBOOST™ is a male desensitizing wipe designed to help temporarily prolong the time until ejaculation.

How do I use PREBOOST™?

Apply a small amount to the head and shaft of the penis before intercourse, or use as directed by a doctor. Be sure to wash the product off after intercourse.

Are there any contraindications for using PREBOOST™?

There are no contraindications listed for PREBOOST™.

What should I do if I accidentally swallow PREBOOST™?

If swallowed, get medical help or contact a poison control center right away.

What should I do if I experience irritation while using PREBOOST™?

If you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a doctor.

Is PREBOOST™ safe to use during pregnancy or while nursing?

There is no specific information regarding the use of PREBOOST™ during pregnancy or nursing in the provided text.

Are there any known drug interactions with PREBOOST™?

No specific drug interactions are mentioned for PREBOOST™.

How should I store PREBOOST™?

Store PREBOOST™ at room temperature and keep it out of reach of children. Discard after opening.

What should I do if PREBOOST™ does not provide relief from premature ejaculation?

If PREBOOST™, used as directed, does not provide relief, discontinue use and consult a doctor.

Packaging Info

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

Packaging configurations for Preboost.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

PREBOOST™ is a male desensitizing wipe designed to temporarily prolong the time until ejaculation. Each unit consists of a single-use, premoistened towelette, facilitating ease of application. The product has been developed by Dr. Harry Fisch and is manufactured for 944 Corp, located at 944 Park Ave, New York, NY 10028. Further information can be found at www.preboost.com.

Uses and Indications

This drug is indicated for the temporary prolongation of the time until ejaculation in adult males.

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

Dosage and Administration

Healthcare professionals should instruct patients to apply a small amount of the product to the head and shaft of the penis prior to intercourse, or as directed by a physician. It is important to ensure that the product is thoroughly washed off after intercourse to maintain proper hygiene and effectiveness.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that if the product is swallowed, immediate medical assistance should be sought or a poison control center contacted.

Warnings and Precautions

Premature ejaculation may indicate an underlying condition that necessitates medical supervision. If the product is used as directed and does not provide relief, it is imperative to discontinue use and seek consultation with a healthcare professional.

Healthcare providers should advise patients to avoid contact with the eyes, as this may lead to irritation or adverse effects.

In the event that either the patient or their partner experiences a rash or irritation, characterized by symptoms such as burning or itching, it is essential to discontinue use immediately. Should symptoms persist despite discontinuation, a consultation with a healthcare provider is recommended to evaluate the situation further.

Side Effects

Patients using this product may experience adverse reactions that necessitate careful monitoring and management. Notably, premature ejaculation may indicate an underlying condition that requires medical supervision. If the product does not provide relief when used as directed, patients are advised to discontinue use and consult a healthcare professional.

In addition, it is important to avoid contact with the eyes, as this may lead to irritation. Should either the patient or their partner develop a rash or experience irritation characterized by burning or itching, it is recommended to discontinue use immediately. Persistent symptoms should prompt consultation with a doctor to ensure appropriate care and management.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

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

Packaging configurations for Preboost.
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

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 currently no information available regarding the use of PREBOOST (benzocaine liquid) during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals should exercise caution when considering the use of this product in pregnant patients due to the lack of data on potential fetal impacts and outcomes. Women of childbearing potential should be advised to discuss their pregnancy status and any potential risks with their healthcare provider before using this product.

Lactation

There are no specific warnings or recommendations regarding the use of this medication in nursing mothers. Additionally, there are no specific warnings or recommendations concerning lactation. Healthcare professionals should consider the absence of data when advising lactating mothers about the use of this medication.

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 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 implement supportive care measures, which may include monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, consultation with a poison control center or a medical toxicologist is recommended to guide the management of the overdose effectively.

Documentation of the incident, including the substance involved, the amount taken, and the time of ingestion, is crucial for appropriate treatment and follow-up care.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

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. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact a poison control center immediately. This guidance is crucial to ensure the safety and well-being of patients and to mitigate any potential risks associated with accidental ingestion.

Storage and Handling

The product is supplied in a configuration that ensures optimal usability. It should be stored at room temperature, away from direct sunlight and moisture. To maintain safety, it is essential to keep the product out of reach of children. Once opened, the product must be discarded to ensure proper handling and safety.

Additional Clinical Information

The product is administered topically, with a recommendation to apply a small amount to the head and shaft of the penis before intercourse, or as directed by a clinician. It is important for patients to wash the product off after intercourse. 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 Preboost, 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 Preboost, 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.