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Skins Delay Climax Control Benzocaine 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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2022
Label revision date
July 16, 2024
Drug Information (PDF)
Prescribing information, PDF file
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
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2022
Label revision date
July 16, 2024
Manufacturer
SKINS SEXUAL HEALTH LIMITED
Registration number
M017
NDC root
81923-365
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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, which can be a concern for many individuals. By using this drug, you may find it easier to manage your sexual performance and enhance your overall experience. If you have questions about how it works or whether it’s right for you, consider discussing it with a healthcare professional for personalized advice.

Uses

If you're looking for a way to manage premature ejaculation, this medication can help. It works by temporarily preventing this condition, allowing for a more satisfying experience. Remember, it's important to discuss any concerns or questions with your healthcare provider to ensure it's the right option for you.

Dosage and Administration

Before engaging in intercourse, you should apply the product directly to the head and shaft of the penis. It's important to massage the product into the skin until it is fully absorbed. After application, make sure to wipe away any excess product to ensure a clean and comfortable experience.

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 crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this product. However, always use it as directed and consult with a healthcare professional if you have any questions or concerns.

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 rash 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. If you have any concerns about these side effects, don’t hesitate to reach out to a healthcare professional.

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 applying it to any internal areas or using it in ways not specified.

Be cautious of any skin reactions, such as rashes, burning, or itching, either on yourself or your partner. If you notice any of these symptoms, stop using the product and reach out to your physician. Additionally, take care to avoid contact with your eyes. If the product is accidentally swallowed, seek medical help or contact a poison control center right away.

Overdose

If you or someone else has swallowed this product, it’s important to seek medical attention right away or contact a 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 get help. Remember, it’s always better to be cautious when it comes to your health.

Pregnancy Use

When it comes to using this medication during pregnancy, there are no specific guidelines or safety concerns provided. It's important to consult with your healthcare provider if you are pregnant, planning to become pregnant, or breastfeeding. They can help you understand any potential risks and make informed decisions about your treatment options. Always prioritize open communication with your doctor to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your physician before using this product. There is a possibility that the ingredients may be passed into your breast milk, and the effects on your nursing infant are not fully understood. Taking these precautions can help ensure the safety and well-being 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 the product, seek medical attention or contact a poison control center right away. 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

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no dosage adjustments, special monitoring, or safety considerations to discuss for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to consult your healthcare provider for personalized advice and guidance.

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 or how your liver health should be considered when taking it.

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 you understand how to manage your liver health while considering any medications you may need.

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

Before using the product, check the foil packaging; do not use it if the foil is damaged, as this could compromise the safety and quality of the device. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You will apply this medication topically, which means you will apply it directly to the skin. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or experiences reported after the medication has been on the market.

FAQ

What is the purpose of this product?

This product helps to temporarily prevent premature ejaculation.

How should I apply the product?

Apply the product to the head and shaft of the penis prior to intercourse, massaging it into the skin until absorbed, and wipe away any excess.

What should I do if the product is swallowed?

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

What should I do if I experience irritation?

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

Is this product safe for external use?

Yes, this product is for external use only. Avoid contact with eyes.

What precautions should nursing mothers take?

Nursing mothers should consult a physician before using this product, as there is a potential for excretion in breast milk and the effects on a nursing infant are unknown.

How should I store this product?

Store the product in a cool, dry place out of direct sunlight, below 30°C (86°F), and do not use if the foil is damaged.

Are there any contraindications for this product?

No specific contraindications are listed for this product.

Packaging Info

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

Packaging configurations for Skins Delay Climax Control Benzocaine Gel.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No specific description details are provided in the text.

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 this condition, providing a therapeutic option to enhance sexual performance and satisfaction.

Dosage and Administration

The product should be applied to the head and shaft of the penis prior to intercourse. Healthcare professionals are advised to instruct patients to massage the product into the skin of the penis until it is fully absorbed. Following application, any excess product should be wiped away to ensure optimal effectiveness and minimize potential side effects.

Contraindications

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

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 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.

In addition, 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 avoid contact with the eyes to prevent potential adverse effects.

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 Skins Delay Climax Control Benzocaine Gel (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Skins Delay Climax Control Benzocaine 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 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

Pregnant patients should be aware that the safety of this medication during pregnancy has not been established. There are no available data regarding the potential risks or fetal outcomes associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to discuss the potential risks and benefits with their patients. It is recommended that healthcare providers remain vigilant and informed about any emerging data related to the use of this medication in pregnant patients.

Lactation

Lactating mothers should consult a physician before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are unknown.

Renal Impairment

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

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 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 assess the patient's condition and consider the appropriate management procedures based on the severity of symptoms and the specific circumstances of the overdosage.

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 imperative to seek medical attention or contact a poison control center immediately. This information is crucial for ensuring patient safety and prompt intervention in the event of accidental ingestion.

Storage and Handling

The product is supplied in a configuration that includes specific packaging details, which are essential for proper handling and storage. It is recommended to store the product in a cool, dry place, ensuring that the temperature remains below 30°C (86°F) and that it is kept out of direct sunlight.

Healthcare professionals should be aware that the product must not be used if the foil packaging is damaged, as this may compromise the integrity of the product. Proper adherence to these storage and handling guidelines is crucial for maintaining the product's efficacy and safety.

Additional Clinical Information

The route of administration for the product is topical. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Skins Delay Climax Control Benzocaine 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 Skins Delay Climax Control Benzocaine 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.