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Powerect Benzocaine Male Delay Gel

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Active ingredient
Benzocaine 50 mg/1 mL
Other brand names
Drug class
Standardized Chemical Allergen
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2022
Label revision date
July 16, 2024
Active ingredient
Benzocaine 50 mg/1 mL
Other brand names
Drug class
Standardized Chemical Allergen
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2022
Label revision date
July 16, 2024
Manufacturer
SKINS SEXUAL HEALTH LIMITED
Registration number
M017
NDC root
81923-367

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 temporarily prevent premature ejaculation, allowing for a more satisfying sexual experience. While the specific details about how it works are not provided, its primary purpose is to support individuals in managing this common concern. If you have questions about how it may fit into your personal health needs, consider discussing it with a healthcare professional.

Uses

If you're looking for a solution to help with premature ejaculation, this medication can be beneficial. It works by temporarily preventing this condition, allowing for a more satisfying experience. If you have concerns about this issue, consider discussing it with your healthcare provider to see if this option is right for you.

Dosage and Administration

To use this product effectively, you should apply it to both the head and shaft of the penis before engaging in intercourse, or follow your doctor's specific instructions. It's important to ensure that you only use the recommended amount. After applying the product, make sure to wipe away any excess to avoid unnecessary mess or irritation. Following these steps will help you achieve the best results.

What to Avoid

It's important to be aware of specific instructions regarding the use of this product. If you accidentally swallow it, you should seek medical attention or contact a poison control center right away. This is a crucial step to ensure your safety and well-being.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this product. However, always prioritize your health by following the recommended guidelines for 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 indicate a condition that needs medical attention. If the product does not help, stop using it and talk to your doctor. Additionally, if you or your partner notice any rashes or irritation, such as burning or itching, discontinue use and seek medical advice.

Remember, this product is for external use only, so be sure to avoid contact with your eyes.

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 when used as directed, please stop using it and consult your doctor. Remember, this product is for external use only, so avoid getting it in your eyes.

Should you or your partner notice any rash or irritation, such as burning or itching, stop using the product and reach out to your physician. In case the product is accidentally swallowed, seek medical help or contact a poison control center right away. Your safety is important, so please take these precautions seriously.

Overdose

If you or someone else has swallowed this product, it’s important to seek medical attention right away or contact your local poison control center. Acting quickly can help ensure safety and proper care.

Signs of an overdose may include unusual symptoms, but specific details about these symptoms are not provided here. If you notice anything concerning, don’t hesitate to reach out for help. Remember, it’s always better to be cautious when it comes to health and safety.

Pregnancy Use

Currently, there is no information available about the use of POWERECT Benzocaine Male Delay Gel during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is essential to consult with your healthcare provider before using this product to ensure your safety and the well-being of 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 while 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 benefits and risks 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 prevent accidental ingestion. If your child swallows any of the product, seek medical attention or contact your local poison control center right away. Taking these precautions can help ensure your child's safety.

Geriatric Use

When considering the use of POWERECT Benzocaine Male Delay Gel for older adults, it's important to note that the drug insert does not provide specific information about its use in this age group. This means there are no established guidelines for dosage adjustments, safety concerns, or special precautions tailored for elderly patients.

If you are an older adult or a caregiver, it’s always a good idea to consult with a healthcare professional before starting any new medication. They can help assess individual health needs and ensure that the treatment is safe and appropriate for you.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for your condition in the provided information. This means that the standard recommendations for medication use may apply to you, but it's always best to consult with your healthcare provider for personalized advice. They can help ensure that any treatment you receive is safe and effective based on your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines, dosage adjustments, or special monitoring instructions provided for your condition in the available information. This means that the medication may not have been studied in depth for its effects on individuals with liver impairment.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have 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 important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place where the temperature stays below 30°C (86°F) and away from direct sunlight. This helps maintain its effectiveness and safety.

When handling the product, be sure to keep it in a clean environment to avoid contamination. Following these simple storage and handling guidelines will help you use the product safely and effectively.

Additional Information

You should apply the product to the head and shaft of the penis before intercourse, or as directed by your doctor. Be sure to wipe away any excess product after application. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is the purpose of this drug?

This drug helps to temporarily prevent premature ejaculation.

How should I use this product?

Apply the product to the head and shaft of the penis prior to intercourse, or as directed by your physician. Be sure to wipe away any excess product.

Are there any warnings I should be aware of?

Yes, if you or your partner develop a rash or irritation, such as burning or itching, discontinue use and consult a physician. This product is for external use only and should not come into contact with your eyes.

What should I do if the product is swallowed?

If the product is swallowed, seek medical attention or contact a poison control center immediately.

Is there any information regarding use during pregnancy or nursing?

There is no specific information provided regarding use during pregnancy or nursing mothers.

How should I store this product?

Store the product in a cool, dry place below 30°C (86°F) and out of direct sunlight.

Are there any contraindications or risks associated with this drug?

No contraindications, abuse risks, or dependence concerns are listed for this drug.

What should I do if the product does not provide relief?

If the product does not provide relief when used as directed, discontinue use and consult a physician, as premature ejaculation may require medical supervision.

Is this product safe for children?

Keep this product out of reach of children.

Packaging Info

Below are the non-prescription pack sizes of Powerect Benzocaine Male Delay Gel (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Powerect Benzocaine Male Delay Gel.
Details

Drug Information (PDF)

This file contains official product information for Powerect Benzocaine Male Delay Gel, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The drug is identified by the SPL code 34089-3 and is formulated as a sterile, non-pyrogenic, isotonic solution. It contains Sodium Chloride as the active ingredient. The solution is characterized by its clear and colorless appearance. Inactive ingredients consist of Water for Injection. The pH of the solution is adjusted to a range of 5.0 to 7.0.

Uses and Indications

This drug is indicated for the temporary prevention of premature ejaculation in adult males. It is intended for use in patients who experience difficulties in controlling ejaculation during sexual activity.

Dosage and Administration

The product should be applied to the head and shaft of the penis prior to intercourse, or as directed by a physician. It is important to wipe away any excess product following application to ensure optimal effectiveness and minimize potential side effects.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek immediate medical attention or contact a poison control center if the product is swallowed.

Warnings and Precautions

Premature ejaculation may indicate an underlying condition that necessitates medical supervision. If the product does not provide relief when used as directed, it is imperative to discontinue use and consult a physician for further evaluation and management.

In the event that either the user or their partner experiences a rash or irritation, including symptoms such as burning or itching, it is essential to discontinue use immediately and seek medical advice.

This product is intended for external use only. Care should be taken to avoid contact with the eyes. In the case of accidental ingestion, it is crucial to seek medical attention or contact a poison control center without delay.

Side Effects

Patients using this product should be aware of several important warnings and potential adverse reactions. 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 physician.

Additionally, if either the patient or their partner experiences a rash or irritation, such as burning or itching, it is recommended to discontinue use and seek medical advice.

This product is intended for external use only, and patients should take care to avoid contact with the eyes to prevent irritation or adverse effects.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Powerect Benzocaine Male Delay Gel (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Powerect Benzocaine Male Delay Gel.
Details

Pediatric Use

Pediatric patients should be advised to keep this product out of reach of children. In the event that the product is swallowed, it is crucial to seek medical attention or contact a poison control center immediately.

Geriatric Use

There is no specific information regarding the use of POWERECT Benzocaine Male Delay Gel in geriatric patients. The prescribing information does not provide guidance on dosage adjustments, safety concerns, or special precautions for elderly patients. Therefore, healthcare providers should exercise caution and consider individual patient factors when prescribing this medication to geriatric patients. Monitoring for efficacy and potential adverse effects is recommended, as the absence of specific data necessitates a careful approach in this population.

Pregnancy

There is currently no information available regarding the use of POWERECT Benzocaine Male Delay Gel during pregnancy. This includes a lack of data on safety concerns, dosage modifications, or any special precautions that should be taken when considering the use of this product in pregnant patients. Healthcare professionals should exercise caution and consider the absence of data when advising women of childbearing potential regarding the use of this product during pregnancy.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution when prescribing this medication to lactating mothers, as the effects on breastfed infants are not well characterized. It is advisable to weigh the potential benefits against any unknown risks when considering treatment options for lactating patients.

Renal Impairment

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

Hepatic Impairment

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise caution and consider the overall clinical context when prescribing this medication to patients with liver problems, as the absence of specific guidance necessitates careful evaluation of potential risks and benefits.

Overdosage

In the event of an overdosage, immediate medical attention is essential. If the product is ingested, healthcare professionals should advise patients or caregivers to seek medical assistance or contact a poison control center without delay.

Prompt intervention is critical to mitigate potential adverse effects associated with overdosage. It is recommended that healthcare providers monitor the patient for any symptoms that may arise as a result of the overdosage. The specific symptoms may vary depending on the nature of the product and the amount ingested, thus thorough assessment and management are necessary.

In managing an overdosage situation, healthcare professionals should follow established protocols for treatment, which may include supportive care and symptomatic management. Continuous monitoring of the patient's vital signs and overall condition is advised to ensure appropriate responses to any complications that may develop.

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

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients that if the product is swallowed, it is crucial to seek medical attention or contact a poison control center immediately. This information is vital for ensuring patient safety and prompt intervention in case of accidental ingestion.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which are essential for identification and inventory management. It is imperative to store the product in a cool, dry place, ensuring that the temperature remains below 30°C (86°F). Additionally, the product should be kept out of direct sunlight to maintain its integrity and efficacy. Proper storage conditions are crucial for preserving the quality of the product throughout its shelf life.

Additional Clinical Information

The product should be applied to the head and shaft of the penis prior to intercourse, or as directed by a physician. It is important for patients to wipe away any excess product after application. 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 Powerect Benzocaine Male Delay Gel, 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 Powerect Benzocaine Male Delay Gel, 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.