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Bonadur

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This product has been discontinued

Active ingredient
Lidocaine Hydrochloride 10 mg/1 mg
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2015
Label revision date
November 20, 2018
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 10 mg/1 mg
Other brand names
Dosage form
Spray
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 2015
Label revision date
November 20, 2018
Manufacturer
WebRx Pharmacy Palace
Registration number
part348
NDC root
70582-999
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

BonaDur is a male genital desensitizing spray that contains lidocaine, a medication that helps reduce sensitivity. It is designed to temporarily slow the onset of ejaculation and prolong the time until ejaculation occurs, which can enhance sexual experience. The rapid-acting formula allows for quick application, making it a convenient option for those seeking to improve their sexual performance.

Uses

If you're looking for a way to manage premature ejaculation, this product may be helpful for you. It contains a male genital desensitizing spray with lidocaine, which is designed to temporarily slow the onset of ejaculation.

The rapid-acting formula works to prolong the time until ejaculation, allowing for a more satisfying experience. By using this spray, you can gain better control during intimate moments.

Dosage and Administration

To use this medication effectively, start by removing the plastic cap from the spray bottle. Before applying, you need to prime the spray pump by pressing the actuator repeatedly until the product dispenses. For your initial dosage, apply 3 sprays to the head and shaft of the penis about 10 minutes before sexual intercourse, but you can use up to 10 sprays if directed by your doctor.

Once you’ve sprayed the product, gently rub it into the skin until it is fully absorbed. After intercourse, make sure to wash the product off. Finally, don’t forget to replace the plastic cap after each use to keep the spray in good condition.

What to Avoid

It's important to be aware of certain situations where you should not use this medication. You should avoid using it if you or your partner are allergic to lidocaine or any topical anesthetics, as this could lead to serious allergic reactions. Additionally, if your partner is pregnant or may become pregnant, you should also refrain from using this medication.

Always prioritize safety by following these guidelines. If you have any concerns or questions about your health or the use of this medication, please consult with a healthcare professional.

Side Effects

You should be aware that this product is for external use only and should not be sprayed on broken, irritated, or sensitive skin. It's important to avoid contact with your eyes. If you or your partner experience any rash or irritation, such as burning or itching, stop using the product and consult a doctor. If these symptoms persist, seek medical advice. Additionally, if you find that the product does not help with premature ejaculation, which may indicate a condition needing medical attention, discontinue use and talk to a doctor.

Before using this product, it's advisable to consult with a doctor or pharmacist if you have any liver problems.

Warnings and Precautions

This product is for external use only, so please avoid spraying it on broken, irritated, or sensitive skin, and keep it away from your eyes. If you have liver problems, it's important to consult with a doctor or pharmacist before using this product.

In case of accidental swallowing, seek medical help or contact a Poison Control Center immediately. If you or your partner experience any rash or irritation, such as burning or itching, stop using the product and consult your doctor. Additionally, if you find that this product does not help with premature ejaculation, which may indicate a condition needing medical attention, please discontinue use and speak with your doctor.

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 attention 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 guidance. Your safety is the top priority, so it's always better to err on the side of caution.

Pregnancy Use

If you are pregnant or planning to become pregnant, it is important to avoid using this medication. This precaution is in place to ensure the safety of both you and your potential child. If your partner is pregnant or may become pregnant, you should also refrain from using this medication. Always consult with your healthcare provider for guidance tailored to your specific situation.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there are no statements indicating that the product is excreted in breast milk or that it poses any risk to your infant. This means you can use the product without concern for its effects on your milk production or your baby's health.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If a child swallows 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 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 if you or a loved one is an older adult, it’s important to consult with a healthcare provider before starting the medication. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

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 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 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 may not have known conflicts with other drugs or 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 medications or upcoming lab tests 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 in a cool, dry place at a temperature between 20°-25° C (68°-77° F). It's important to keep it away from fire and flames to prevent any hazards.

When handling the product, always maintain a clean environment to avoid contamination. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically by spraying it on the head and shaft of the penis, using 3 to 10 sprays about 10 minutes before sexual intercourse, or as directed by your doctor. It's important to consult with a doctor or pharmacist before using this product if you have liver problems, are allergic to lidocaine or other topical anesthetics, or if your partner is pregnant or may become pregnant.

If you or your partner experience any rash or irritation, such as burning or itching, stop using the product and consult a doctor. Additionally, if you find that this product does not help with premature ejaculation, which may indicate a condition needing medical attention, discontinue use and seek advice from a healthcare professional.

FAQ

What is BonaDur?

BonaDur is a male genital desensitizing spray that contains lidocaine, designed to help temporarily slow the onset of ejaculation.

How does BonaDur work?

BonaDur works by using a rapid-acting lidocaine-based formula to help temporarily prolong the time until ejaculation.

How should I use BonaDur?

Remove the plastic cap, prime the spray pump, and apply 3 or more sprays (not to exceed 10) to the head and shaft of the penis 10 minutes before sexual intercourse.

What should I do after using BonaDur?

You should rub BonaDur into the skin until fully absorbed and wash it off after intercourse.

Are there any contraindications for using BonaDur?

Do not use BonaDur if you or your partner are allergic to lidocaine or topical anesthetics, or if your partner is or may become pregnant.

What are the warnings associated with BonaDur?

BonaDur is for external use only, should not be sprayed on broken or sensitive skin, and contact with the eyes should be avoided.

What should I do if I experience irritation after using BonaDur?

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

What should I do if BonaDur is swallowed?

If swallowed, seek medical help or contact a Poison Control Center immediately.

How should BonaDur be stored?

Store BonaDur at 20°-25° C (68°-77° F) and keep it away from fire and flame.

Is there any specific information for patients with liver problems?

You should ask a doctor or pharmacist before using BonaDur if you have liver problems.

Packaging Info

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

Packaging configurations for Bonadur.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

This male genital desensitizing spray contains lidocaine as its active ingredient. It is designed to temporarily prolong the time until ejaculation. The formulation is characterized by its rapid-acting properties, providing quick onset of action. The product is available in a net volume of 0.25 fluid ounces (7.4 milliliters).

Uses and Indications

This drug is indicated for the temporary management of premature ejaculation in adult males. It is a male genital desensitizing spray formulated with lidocaine, designed to help temporarily slow the onset of ejaculation and prolong the time until ejaculation occurs. The rapid-acting lidocaine-based formula provides a quick onset of action, facilitating improved control during sexual activity.

Dosage and Administration

The plastic cap should be removed prior to use. To prime the spray pump, the actuator must be pressed repeatedly until the product dispenses. The recommended initial dosage is 3 sprays, which may be applied to the head and shaft of the penis. The application should occur 10 minutes before sexual intercourse or as directed by a healthcare professional. The total number of sprays should not exceed 10.

After application, the product should be rubbed into the skin of the penis until fully absorbed. It is important to wash the product off after intercourse. Following each use, the plastic cap should be replaced to maintain the integrity of the spray pump.

Contraindications

Use is contraindicated in individuals with a known allergy to lidocaine or other topical anesthetics. Additionally, the product should not be used in patients whose partners are pregnant or may become pregnant, due to potential risks to fetal development.

Warnings and Precautions

For external use only. This product should not be sprayed on broken, irritated, or sensitive skin, as such application may exacerbate irritation or cause adverse reactions. Care should be taken to avoid contact with the eyes, as this may lead to significant discomfort or injury.

Healthcare professionals should advise patients to consult a doctor or pharmacist prior to use if they have any liver problems, as underlying conditions may affect the safety and efficacy of the product.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center contacted without delay.

Patients are instructed to discontinue use and consult a healthcare provider if they or their partner experience any rash or irritation, including symptoms such as burning or itching. Should these symptoms persist, further medical evaluation is warranted. Additionally, if premature ejaculation occurs, it may indicate an underlying condition that requires medical supervision. If the product does not provide relief when used as directed, patients should cease use and seek advice from a healthcare professional.

Side Effects

Patients using this product may experience a range of adverse reactions. Serious adverse reactions include the development of a rash or irritation, such as burning or itching, which necessitates discontinuation of use and consultation with a healthcare professional. Additionally, premature ejaculation may indicate an underlying condition that requires medical supervision; if the product does not provide relief when used as directed, patients should discontinue use and seek medical advice.

Common adverse reactions are primarily related to the product's application. It is important to note that this product is for external use only and should not be sprayed on broken, irritated, or sensitive skin. Patients are also advised to avoid contact with the eyes to prevent irritation.

Before using this product, patients should consult a doctor or pharmacist if they have liver problems, as this may influence the safety and efficacy of the treatment.

Drug Interactions

No specific drug interactions or laboratory test interactions are documented in the available data. Therefore, there are no recommendations for dosage adjustments or monitoring related to drug interactions. It is advisable for healthcare professionals to remain vigilant and consult relevant resources for any updates or additional information regarding potential interactions.

Packaging & NDC

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

Packaging configurations for Bonadur.
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 available 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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

Pregnant patients should not use this medication if their partner is or may become pregnant. The potential risks associated with exposure during pregnancy have not been established, and the implications for fetal outcomes remain unclear. Healthcare professionals are advised to counsel women of childbearing potential regarding the importance of effective contraception during treatment and to discuss the potential risks to a developing fetus.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there are no statements concerning the potential for excretion in breast milk or any associated risks to breastfed infants.

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 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 Structured Product Labeling (SPL), healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdosage.

Healthcare providers should monitor patients closely for any potential symptoms that may arise from an overdose. Symptoms may vary depending on the substance involved and the individual patient's response. In the event of an overdosage, it is recommended that healthcare professionals initiate supportive care and symptomatic treatment as necessary.

Management procedures should include the following steps:

  1. Assessment: Conduct a thorough evaluation of the patient's clinical status, including vital signs and level of consciousness.

  2. Supportive Care: Provide appropriate supportive measures, which may include intravenous fluids, oxygen supplementation, and monitoring of cardiac and respiratory function.

  3. Consultation: Engage with a poison control center or a medical toxicologist for guidance on specific interventions and antidotes, if applicable.

Due to the lack of specific overdosage data, it is imperative that healthcare professionals remain vigilant and utilize their clinical judgment in managing any cases of suspected overdosage.

Nonclinical Toxicology

The potential for teratogenic effects is a consideration for individuals who are pregnant or may become pregnant. It is advised that the product not be used in individuals with a known allergy to lidocaine or other topical anesthetics, as this may lead to non-teratogenic adverse effects.

No relevant information is available regarding nonclinical toxicology or animal pharmacology and toxicology.

Postmarketing Experience

Reports of serious adverse events associated with the use of the product have been received through voluntary reporting and surveillance programs. Healthcare professionals and consumers are encouraged to report any serious adverse events by contacting 1-877-797-2522 within the United States.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of the reach of children. Instruct patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use this product if they or their partner are allergic to lidocaine or other topical anesthetics, or if their partner is pregnant or may become pregnant.

Healthcare providers should counsel patients to stop using the product and consult a doctor if they or their partner experience any rash or irritation, such as burning or itching. If these symptoms persist, further medical consultation is recommended. Additionally, patients should be made aware that premature ejaculation may indicate an underlying condition that requires medical supervision. If the product does not provide relief when used as directed, they should discontinue use and seek medical advice.

It is also important for healthcare providers to remind patients to consult a doctor or pharmacist before using this product if they have liver problems.

Storage and Handling

The product is supplied in various configurations, with specific NDC numbers available for identification. It is essential to store the product at a controlled temperature range of 20° to 25° C (68° to 77° F).

Care should be taken to keep the product away from fire and flame to ensure safety and integrity. Proper storage conditions are crucial for maintaining the quality and efficacy of the product.

Additional Clinical Information

The product is administered topically, with a recommended application of 3 to 10 sprays to the head and shaft of the penis, ideally 10 minutes prior to sexual intercourse or as directed by a healthcare professional.

Clinicians should counsel patients to consult a doctor or pharmacist before use if they have liver problems. The product should not be used if the patient or their partner is allergic to lidocaine or other topical anesthetics, or if there is a possibility of pregnancy. Patients are advised to discontinue use and seek medical advice if they or their partner experience any rash or irritation, such as burning or itching. Additionally, if premature ejaculation persists despite proper use of the product, medical consultation is recommended.

Drug Information (PDF)

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