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Prolong

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This product has been discontinued

Active ingredient
Benzocaine 2833 mg/60 mL
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2016
Label revision date
August 7, 2016
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 2833 mg/60 mL
Other brand names
Dosage form
Gel
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 2016
Label revision date
August 7, 2016
Manufacturer
Product Max Group Inc
Registration number
part348
NDC root
70742-089
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

PROLONG is a lubricating gel designed to help prolong sexual pleasure by acting as a benzocaine male genital desensitizer. It works by preventing premature ejaculation, allowing for a more satisfying sexual experience. This product comes in a 2 fluid ounce (60 ml) bottle and is distributed by Body Action Products.

Uses

If you're looking for a solution to help with premature ejaculation, this medication may be beneficial for you. It is specifically designed to assist in preventing this condition, allowing for a more satisfying experience during intimate moments. By addressing premature ejaculation, it aims to enhance your overall sexual health and confidence.

Dosage and Administration

To use this medication effectively, you should apply a small amount to the head and shaft of your penis before engaging in intercourse. This helps ensure that the medication works as intended. After intercourse, it’s important to wash the product off thoroughly to maintain hygiene and prevent any potential irritation. Following these steps will help you get the most benefit from the medication.

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 immediately or contact a Poison Control Center. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this medication. However, always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

When using this product, it's important to remember that it is for external use only and should not come into contact with your eyes. If you experience premature ejaculation, it may indicate an underlying condition that needs medical attention. If the product does not help as expected, stop using it and talk to your doctor.

Additionally, if you or your partner notice any rash or irritation, such as burning or itching, discontinue use immediately. Should these symptoms continue, please consult a healthcare professional for further advice.

Warnings and Precautions

This product is intended for external use only, so be sure to avoid contact with your eyes. If you experience any rash or irritation, such as burning or itching, stop using the product immediately. If these symptoms continue, please consult your doctor.

If you find that this product does not help with premature ejaculation, it may indicate a condition that requires medical attention. In such cases, discontinue use and speak with your doctor. Additionally, if the product is accidentally swallowed, seek medical help or contact a Poison Control Center right away.

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

When considering the use of PROLONG - benzocaine gel during pregnancy, it's important to note that the drug insert does not provide specific information about its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that there is no clear guidance on how the gel may affect you or your developing baby.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before using any medication, including topical products like benzocaine gel. They can help you weigh the potential risks and benefits based on your individual circumstances.

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 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. 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 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 considering the use of PROLONG - benzocaine gel for older adults, it's important to note that the drug insert does not provide specific information about how it may affect this age group. This means there are no special dosage adjustments, safety concerns, or precautions outlined for elderly patients.

As a caregiver or older adult, you should always consult with a healthcare professional before using any new medication. They can help determine if this product is appropriate for you, taking into account your overall health and any other medications you may be using.

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 kidney function might affect the use of this medication.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific condition. They can help determine the best approach based on your kidney health.

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 how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

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 this medication is generally considered safe to use alongside other treatments and tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions or express any concerns you may have regarding your medications or tests.

Storage and Handling

To ensure your product remains safe and effective, always check that the safety seal under the cap is intact before use. If the seal is broken or missing, do not use the product, as this could compromise its safety and effectiveness.

For optimal storage, keep the product in a cool, dry place away from direct sunlight. Following these guidelines will help you handle the product safely and maintain its quality.

Additional Information

No further information is available.

FAQ

What is PROLONG?

PROLONG is a benzocaine male genital desensitizer that helps prolong sexual pleasure and is available as a lubricating gel.

How does PROLONG work?

PROLONG helps in the prevention of premature ejaculation by desensitizing the genital area.

How should I use PROLONG?

Apply a small amount to the head and shaft of the penis before intercourse, and wash the product off after intercourse.

Are there any contraindications for using PROLONG?

No specific contraindications are listed for PROLONG.

What should I do if I swallow PROLONG?

If swallowed, get medical help or contact a Poison Control Center right away.

What precautions should I take when using PROLONG?

For external use only, avoid contact with the eyes, and discontinue use if you or your partner develop a rash or irritation.

Is there any information about using PROLONG during pregnancy or while nursing?

No specific information is provided regarding the use of PROLONG during pregnancy or lactation.

What should I do if the safety seal under the cap is broken or missing?

Do not use PROLONG if the safety seal under the cap is broken or missing.

Where can I find more information about PROLONG?

You can find more information on the website www.bodyactionproducts.com.

Packaging Info

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

Packaging configurations for Prolong.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Benzocaine Male Genital Desensitizer, marketed under the name PROLONG, is a lubricating gel specifically formulated for men. This product is designed to help prolong sexual pleasure. It is available in a dosage form of 2 fluid ounces (60 ml).

Uses and Indications

This drug is indicated for the prevention of premature ejaculation in adult males. It is intended for use in patients who experience difficulties in controlling ejaculation, thereby enhancing sexual satisfaction and overall quality of life.

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. It is essential that the product is thoroughly washed off after intercourse to ensure proper hygiene and effectiveness.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that if the product is swallowed, medical assistance should be sought immediately or contact a Poison Control Center.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes to prevent irritation or injury.

Premature ejaculation may indicate an underlying condition that necessitates medical supervision. If the product, when used as directed, fails to provide relief, it is advised to discontinue use and consult a healthcare professional for further evaluation.

In the event that either the user or their partner experiences a rash or irritation, such as burning or itching, it is essential to discontinue use immediately. Should these symptoms persist, seeking medical advice is recommended.

In cases of accidental ingestion, prompt medical assistance should be sought, or the individual should contact a Poison Control Center without delay.

Side Effects

Patients using this product should be aware that it is intended for external use only and must avoid contact with the eyes. In clinical practice, it has been noted that premature ejaculation may be indicative of an underlying condition that requires medical supervision. If the product, when used as directed, does not provide the desired relief, patients are advised to discontinue use and consult a healthcare professional.

Additionally, if either the patient or their partner experiences a rash or irritation, such as burning or itching, it is recommended to discontinue use immediately. Should these symptoms persist, seeking medical advice is strongly encouraged.

Drug Interactions

No specific drug interactions have been identified for this medication. Additionally, there are no reported interactions with laboratory tests. 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 Prolong (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Prolong.
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 dosage adjustments, safety concerns, or special precautions outlined in the drug insert for PROLONG - benzocaine gel. As there is no available information regarding the use of this medication in geriatric populations, healthcare providers should exercise caution when prescribing to elderly patients. It is advisable to monitor these patients closely for any adverse effects or unusual responses to treatment, given the lack of targeted data for this demographic.

Pregnancy

There are no specific statements regarding the use of PROLONG (benzocaine gel) during pregnancy, including safety concerns, dosage modifications, or special precautions. As such, the potential risks to pregnant patients and fetal outcomes remain undefined. Healthcare professionals should exercise caution when considering the use of this product in women of childbearing potential and weigh the benefits against any potential risks. Further studies may be necessary to establish a clearer understanding of the implications of benzocaine gel use 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 and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established.

Renal Impairment

Patients with renal impairment may not have specific information regarding dosage adjustments, special monitoring, or safety considerations outlined in the prescribing information. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment and monitoring of these patients.

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, as the clinical presentation can vary depending on the substance involved. Common symptoms of overdose may include, but are not limited to, altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and ensuring adequate circulation. The use of activated charcoal may be considered if the patient presents within a suitable timeframe and is deemed appropriate based on clinical judgment.

Furthermore, it is recommended to consult local poison control centers or toxicology experts for guidance on specific management strategies tailored to the individual case. Continuous monitoring and supportive care remain paramount until the patient stabilizes or further interventions are deemed necessary.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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. In the event that the medication is swallowed, patients should be instructed to seek medical help or contact a Poison Control Center immediately. It is important for patients to understand the potential risks associated with improper use and the necessary steps to take in case of an emergency.

Storage and Handling

The product is supplied with a safety seal under the cap, which must remain intact. If the safety seal is broken or missing, the product should not be used.

Storage conditions require the product to be kept in a cool, dry place, away from direct sunlight and moisture. It is essential to ensure that the container is securely closed when not in use to maintain product integrity. Special handling precautions should be observed to prevent damage to the packaging and to ensure the safety seal remains intact.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Prolong, 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 Prolong, 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.