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Lubelife Climax Control Delay

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Active ingredient
Benzocaine 7.5 g/100 mL
Other brand names
Drug class
Standardized Chemical Allergen
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 2022
Label revision date
September 9, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 7.5 g/100 mL
Other brand names
Drug class
Standardized Chemical Allergen
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 2022
Label revision date
September 9, 2025
Manufacturer
CC Wellness LLC
Registration number
M017
NDC root
71683-005
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

This medication is designed for temporary male genital desensitization, which means it can help reduce sensitivity in that area. By doing so, it assists in slowing the onset of ejaculation, potentially helping men who experience premature ejaculation. If you're looking for a way to manage this condition, this medication may be a suitable option to consider.

Uses

If you're looking for a way to enhance your sexual experience, this medication can be beneficial. It is designed for temporary male genital desensitization, which means it can help reduce sensitivity in the genital area. This can be particularly useful if you want to prolong the experience.

Additionally, this medication helps to slow the onset of ejaculation, allowing you to enjoy intimacy for a longer period. By addressing these aspects, it aims to improve your overall sexual satisfaction.

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 will help ensure that you maintain proper hygiene and the effectiveness of the treatment. Always remember to follow the recommended usage for the best results.

What to Avoid

It's important to use this medication safely to avoid any potential issues. You should never get it into your eyes or nostrils, and inhaling it is also not recommended. To ensure your safety, make sure not to exceed 20 sprays within a 24-hour period.

By following these guidelines, you can help prevent any adverse effects and use the medication effectively. Always prioritize your health and well-being when using any treatment.

Side Effects

If you are allergic to local anesthetics or any of the other ingredients in this product, it is important not to use it, as this could lead to serious allergic reactions. Additionally, avoid applying this product on broken or inflamed skin, as it may cause further irritation or complications. Always consult with a healthcare professional if you have any concerns about using this product safely.

Warnings and Precautions

This product is for external use only, so please avoid contact with your eyes, nostrils, and do not inhale it. If you are allergic to local anesthetics or any of the ingredients listed, do not use this product. It should not be applied to broken or inflamed skin, and if your partner is pregnant or if you have a history of liver or kidney problems, consult your doctor before use.

Make sure to use the minimum amount that works for you, and do not exceed 20 sprays in a 24-hour period. Allow 5-15 minutes for the product to dry before engaging in intercourse. If you or your partner experience any rash, burning, or itching, stop using the product immediately and consult a doctor if symptoms persist. If this product does not help with premature ejaculation, or if you suspect an overdose, seek medical attention right away.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include unusual drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, contact your local emergency services or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

If you are pregnant or planning to become pregnant, it’s important to consult with your doctor before using this medication. Your healthcare provider can help you understand any potential risks and ensure that you make informed decisions for your health and the health of your baby. Always prioritize open communication with your doctor regarding any medications you may be considering during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it’s important to consult your doctor before using this product. Currently, there is no specific information available about whether this product can pass into breast milk or what risks it may pose to your baby. Your healthcare provider can help you weigh the benefits and any potential concerns to ensure the safety of both you and your infant.

Pediatric Use

It's important to keep this medication out of reach of children. This precaution helps prevent accidental ingestion, which can be dangerous. Always store it in a safe place where children cannot access it, ensuring their safety at all times. If you have any concerns or questions about the medication, don't hesitate to reach out to your healthcare provider for guidance.

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 consult your doctor before using this medication. Kidney issues can affect how your body processes certain drugs, so your doctor may need to adjust your dosage or monitor you more closely. Always prioritize your health by discussing any existing conditions with your healthcare provider.

Hepatic Impairment

If you have liver (hepatic) or kidney issues, it’s important to consult your doctor before using this medication. Your healthcare provider can help determine if it’s safe for you and may suggest necessary adjustments to your dosage or monitoring based on your specific condition. Always prioritize your health by discussing any concerns with your doctor.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual’s health situation is unique, and your provider can help ensure that your treatment plan is safe and effective for you. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

Storage and Handling

To ensure the safety and effectiveness of your product, it’s important to store it properly. Keep it in a cool, dry place at a temperature between 20-30°C (68-77°F). Avoid exposing the product to heat or flame, as this can compromise its integrity and safety.

When handling the product, always do so with care to maintain a sterile environment (a clean area free from germs). Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is the purpose of this product?

This product is used for temporary male genital desensitization and helps to slow the onset of ejaculation.

How should I apply this product?

Apply a small amount to the head and shaft of the penis before intercourse, or use as directed by a doctor.

What precautions should I take when using this product?

Do not get the product into your eyes or nostrils, do not inhale it, and do not exceed 20 sprays in 24 hours.

How long should I wait after applying the product before intercourse?

Allow 5-15 minutes for the product to dry prior to intercourse.

What should I do if I experience irritation or a rash?

If you or your partner develop a rash or irritation, discontinue use and consult a doctor if symptoms persist.

Can I use this product if my partner is pregnant?

You should ask a doctor before use if your partner is pregnant.

Is this product safe for individuals with liver or kidney problems?

If you have or have had liver or kidney problems, you should ask a doctor before using this product.

What should I do if I accidentally overdose on this product?

Seek medical attention immediately in case of overdose.

Where should I store this product?

Store the product at 20-30°C (68-77°F) and keep it out of reach of children.

Can nursing mothers use this product?

Nursing mothers should consult a doctor before using this product, as there is no specific information regarding its safety during lactation.

Packaging Info

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

Packaging configurations for Lubelife Climax Control Delay.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for temporary male genital desensitization. It is designed to help slow the onset of ejaculation in adult males.

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

Contraindications

Use is contraindicated in patients who may come into contact with the eyes or nostrils, as exposure can lead to irritation or adverse effects. Inhalation of the product is also contraindicated due to potential respiratory complications. Additionally, exceeding the maximum recommended dosage of 20 sprays within a 24-hour period is contraindicated to prevent possible overdose or related adverse reactions.

Warnings and Precautions

For external use only, this product should be applied with caution to avoid contact with the eyes. Healthcare professionals should advise patients to refrain from using this product if they have a known allergy or sensitivity to local anesthetics or any of the other listed ingredients. It is contraindicated for use on broken or inflamed skin.

Prior to use, it is essential to consult a healthcare provider if the partner is pregnant or if the patient has a history of liver or kidney problems. The product must not be applied to the eyes or nostrils, and inhalation should be strictly avoided.

Patients should adhere to the recommended dosage, which should not exceed 20 sprays within a 24-hour period. It is advised to use the minimum effective amount necessary for individual needs. Additionally, the product should be allowed to dry for 5-15 minutes before engaging in intercourse to ensure optimal effectiveness.

Premature ejaculation may indicate an underlying condition that requires medical evaluation. If the product does not provide relief when used as directed, patients should discontinue use and seek medical advice. In the event of a rash or irritation, such as burning or itching, the use of the product should be stopped immediately, and if symptoms persist, consultation with a healthcare professional is recommended.

Patients must strictly follow the usage instructions provided. In case of overdose, immediate medical attention should be sought.

Side Effects

Patients should be aware of the potential for allergic reactions associated with the use of this product. It is contraindicated in individuals who are allergic or sensitive to local anesthetics or any of the other listed ingredients.

Additionally, the product should not be applied to broken or inflamed skin, as this may exacerbate adverse reactions or lead to complications. It is essential for patients to adhere to these guidelines to minimize the risk of serious adverse effects.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

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

Packaging configurations for Lubelife Climax Control Delay.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. Safety and efficacy in pediatric populations have not been established, and caution is advised when administering this medication to younger individuals.

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

Pregnancy

Pregnant patients should consult a healthcare professional before using this medication, particularly if their partner is pregnant. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes are not fully established. It is essential for women of childbearing potential to discuss their reproductive plans and any potential exposure to this medication with their healthcare provider to ensure appropriate management and monitoring.

Lactation

Lactating mothers are advised to consult a doctor prior to using this product. Currently, there is no specific information available regarding the potential for excretion of this product in breast milk or any associated risks to breastfed infants.

Renal Impairment

Patients with renal impairment should consult a healthcare professional prior to use, particularly if they have a history of kidney problems. It is essential to assess renal function and consider potential dosing adjustments or monitoring requirements based on the degree of impairment.

Hepatic Impairment

Patients with hepatic impairment should consult a healthcare professional prior to use, particularly if they have a history of liver or kidney problems. It is essential for these patients to receive appropriate evaluation and monitoring to assess their liver function and determine the suitability of treatment. Adjustments to dosage or specific restrictions may be necessary based on the severity of hepatic impairment, and ongoing monitoring of liver function may be warranted throughout the course of therapy.

Overdosage

In the absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant and prepared for potential scenarios involving overdose.

Healthcare providers should be aware that the clinical presentation of an overdose may vary significantly depending on the substance involved and the individual patient’s characteristics. Symptoms of overdose can range from mild to severe and may include altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of suspected overdosage, immediate medical evaluation is recommended. Healthcare professionals should assess the patient's vital signs and conduct a thorough clinical examination. Supportive care should be initiated as necessary, which may include airway management, intravenous fluids, and monitoring of vital parameters.

If specific antidotes or treatments are available for the substance involved, they should be administered according to established protocols. Consultation with a poison control center or a medical toxicologist may also be beneficial in managing the case effectively.

It is crucial to document all findings and interventions thoroughly, as this information may be vital for ongoing patient management and for any necessary reporting to regulatory authorities.

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

Postmarketing experience has identified the following adverse reactions reported voluntarily or through surveillance programs: rash, irritation, burning, and itching. These events have been documented in the context of routine pharmacovigilance activities.

Patient Counseling

Healthcare providers should advise patients to avoid contact with the eyes and nostrils when using this product. Patients should be informed not to inhale the product and to adhere strictly to the recommended dosage, which should not exceed 20 sprays within a 24-hour period. It is important to emphasize the necessity of using the minimum effective amount to achieve desired results.

Patients should be instructed to allow 5-15 minutes for the product to dry prior to engaging in sexual intercourse. Providers should discuss the possibility that premature ejaculation may be indicative of an underlying condition that requires medical supervision. If the product does not provide relief when used as directed, patients should be advised to discontinue use and consult a healthcare professional.

Additionally, patients should be made aware that if they or their partner experience any rash or irritation, such as burning or itching, they should stop using the product immediately. If symptoms persist, it is essential to seek medical advice. The product can be utilized for both sexual intercourse and sex play, provided it is applied according to the usage instructions. In the event of an overdose, patients should be instructed to seek medical attention without delay.

Storage and Handling

The product is supplied in configurations that adhere to the National Drug Code (NDC) standards. It is essential to store the product at a controlled temperature range of 20-30°C (68-77°F). Care should be taken to avoid exposure to heat or flame during storage and handling to maintain product integrity.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Lubelife Climax Control Delay, 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 Lubelife Climax Control Delay, 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.