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Popstar

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Active ingredient
Lidocaine Hydrochloride 10 mg/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2025
Label revision date
December 12, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 10 mg/100 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2025
Label revision date
December 12, 2025
Manufacturer
Pineapple Brands LLC
Registration number
M017
NDC root
85035-111
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 slow the onset of ejaculation. It can be beneficial for individuals seeking to manage premature ejaculation, allowing for a more satisfying sexual experience. While the specific details of how it works are not provided, its primary purpose is to assist in enhancing sexual performance by addressing this common concern.

Uses

If you're looking for a way to manage premature ejaculation, this medication can help by temporarily slowing the onset of ejaculation. This means it may give you more control during intimate moments, potentially enhancing your overall experience. Always consult with a healthcare professional to see if this treatment is right for you.

Dosage and Administration

To use this medication effectively, start by gently shaking the bottle to mix the contents. Next, hold the bottle upright and press the pump to dispense the spray. You should apply 3 or more sprays, but do not exceed 10 sprays total, directly to the head and shaft of the penis. It's best to do this about 10 minutes before you plan to have intercourse, or follow your doctor's specific instructions.

After intercourse, make sure to wash the product off thoroughly. This will help ensure that you maintain proper hygiene and avoid any potential irritation. Always follow the recommended guidelines for use to achieve the best results.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. While there are no listed contraindications, controlled substance classifications, or concerns about abuse or dependence, you should take care if the medication is swallowed. In such a case, seek medical attention or contact a Poison Control Center immediately. Your safety is paramount, so please follow these guidelines closely.

Side Effects

If you are considering using this product, it's important to be aware of some potential side effects and warnings. You should not use it if you or your partner are allergic to lidocaine or other topical anesthetics. Avoid getting the spray in your eyes, and do not apply it to broken, irritated, or sensitive skin.

If you notice that the product does not provide relief as expected, or if you or your partner experience any rash or irritation, such as burning or itching, stop using it and consult a doctor. These reactions may indicate a need for medical attention.

Warnings and Precautions

This product is for external use only, so please avoid applying it to broken, irritated, or sensitive skin. If you or your partner are allergic to lidocaine or other topical anesthetics, do not use this product. Be careful to keep it away from your eyes, and if you experience any rash or irritation, such as burning or itching, stop using it and consult your doctor.

If you find that this product does not relieve your symptoms as directed, it's important to stop using it and speak with your doctor, as premature ejaculation may indicate a condition that needs medical attention. Additionally, if you have liver problems or if your partner is pregnant or may become pregnant, consult with a doctor or pharmacist before using this product. In case of accidental swallowing, seek medical help or contact a Poison Control Center right away.

Overdose

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

In case of an emergency, call your local emergency number 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 or pharmacist before using this medication. This is especially crucial if your partner is pregnant or may become pregnant, as certain medications can affect pregnancy outcomes. Always prioritize open communication with your healthcare provider to ensure the safety of both you and your baby.

Lactation Use

If you are breastfeeding, you can use Popstar Delay Spray without specific warnings or recommendations against it. Currently, there is no information available about whether the ingredients in this spray pass into breast milk or if they pose any risks to your baby. As always, if you have concerns or questions about using any product while nursing, it's a good idea to consult with your healthcare provider for personalized advice.

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 or contact a Poison Control Center right away. Taking these precautions can help ensure your child's safety.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

Renal Impairment

If you have kidney problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

Hepatic Impairment

If you have liver problems, it's important to consult with your doctor or pharmacist before using this medication. They can provide guidance on whether it's safe for you and if any adjustments to your dosage are necessary. Your liver plays a crucial role in processing medications, so ensuring that you have the right support is essential for your health. Always prioritize open communication with your healthcare team regarding your liver condition.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you. Always share your complete list of medications and any health conditions you have to receive the best care possible.

Storage and Handling

To ensure the best performance of your product, remember to remove the safety tab before use. It's also important to store the product in a cool, dry place, ideally at a temperature between 68° and 77° F (20-25° C). This temperature range helps maintain the product's effectiveness and safety.

Handling the product with care is essential. Always ensure that you follow these storage guidelines to avoid any potential issues. If you have any questions about disposal or further safety measures, please consult the product instructions or your healthcare provider.

Additional Information

You should apply this medication topically by spraying it on the head and shaft of the penis. Use 3 to 10 sprays about 10 minutes before intercourse, or follow your doctor's instructions. Make sure not to exceed the recommended number of sprays. If you have any questions or concerns about how to use this medication, consult your healthcare provider for guidance.

FAQ

What is the purpose of this drug?

This drug helps in temporarily slowing the onset of ejaculation.

How do I use this spray?

Gently shake the bottle, hold it upright, and press the pump until the spray dispenses. Apply 3 or more sprays, not to exceed 10, to the head and shaft of the penis 10 minutes before intercourse.

What should I do after using the spray?

You should wash the product off after intercourse.

Are there any warnings I should be aware of?

Do not use if you or your partner are allergic to lidocaine or topical anesthetics, and avoid contact with the eyes. Stop using and consult a doctor if you or your partner develop a rash or irritation.

What should I do if the spray is swallowed?

If swallowed, get medical attention or contact a Poison Control Center immediately.

Can I use this spray if my partner is pregnant?

Ask a doctor or pharmacist before use if your partner is, or may be, pregnant.

Is this spray safe for nursing mothers?

There are no specific warnings or recommendations regarding the use of this spray in nursing mothers.

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

Stop using the product and ask a doctor, as premature ejaculation may require medical supervision.

How should I store this spray?

Store the spray at 68°-77° F (20-25° C) and keep it out of reach of children.

Packaging Info

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

Packaging configurations for Popstar.
Details

Drug Information (PDF)

This file contains official product information for Popstar, 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 drug.

Uses and Indications

This drug is indicated for the temporary slowing of the onset of ejaculation in adult males. It is intended for use in patients experiencing premature ejaculation. The efficacy of this drug is limited to the management of this specific condition and should be used as part of a comprehensive treatment plan that may include counseling and behavioral techniques.

Dosage and Administration

Healthcare professionals should instruct patients to gently shake the bottle prior to use. The product should be held upright, and the pump should be pressed until the spray dispenses. Patients are advised to apply 3 or more sprays, not exceeding a total of 10 sprays, to both the head and shaft of the penis. This application should occur approximately 10 minutes before intercourse or as directed by a healthcare provider. It is important for patients to wash the product off after intercourse to ensure proper hygiene.

Contraindications

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

Warnings and Precautions

For external use only, this product is contraindicated in individuals with a known allergy to lidocaine or other topical anesthetics. Healthcare professionals should advise patients to avoid contact with the eyes, as this may lead to irritation or injury.

It is imperative that the product not be applied to broken, irritated, or sensitive skin to prevent adverse reactions. Should the product fail to provide relief when used as directed, or if premature ejaculation is suspected to be due to an underlying condition, patients are advised to discontinue use and consult a healthcare provider for further evaluation.

In the event that either the patient or their partner experiences a rash or irritation, such as burning or itching, they should cease use immediately and seek medical advice.

Patients with liver problems should consult a doctor or pharmacist prior to using this product, as liver function may affect the metabolism of lidocaine. Additionally, if the partner is pregnant or may become pregnant, it is essential to seek guidance from a healthcare professional before use.

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

Side Effects

Patients should be aware of the following warnings associated with the use of this product. It is contraindicated in individuals who are allergic to lidocaine or other topical anesthetics. Care should be taken to avoid contact with the eyes, as this may lead to adverse effects. Additionally, the product should not be sprayed on broken, irritated, or sensitive skin to prevent potential complications.

In the event that the product does not provide relief when used as directed, patients are advised to stop use and consult a healthcare professional, as premature ejaculation may indicate an underlying condition that requires medical supervision. Furthermore, 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.

Drug Interactions

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

Packaging & NDC

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

Packaging configurations for Popstar.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of accidental ingestion, it is crucial to seek medical attention or contact a Poison Control Center immediately.

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 consult a healthcare professional before using this medication, especially if their partner is, or may be, pregnant. The potential risks and effects on fetal outcomes have not been fully established, and caution is advised to ensure the safety of both the patient and the developing fetus. It is important for women of childbearing potential to discuss their reproductive plans with their healthcare provider prior to initiating treatment.

Lactation

There are no specific warnings or recommendations regarding the use of Popstar Delay Spray in lactating mothers. Additionally, there is no information available about the potential for excretion of the product in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in this patient population.

Hepatic Impairment

Patients with hepatic impairment should consult a healthcare professional, such as a doctor or pharmacist, prior to using this medication. It is essential for patients with liver problems to receive appropriate guidance to ensure safe and effective use of the drug. Monitoring of liver function may be necessary, and dosage adjustments could be required based on the severity of the hepatic impairment.

Overdosage

In the absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may arise from an overdose. Common symptoms may include, but are not limited to, severe drowsiness, confusion, respiratory distress, or any other unusual clinical manifestations.

Management of an overdose should be tailored to the individual patient and may involve supportive care, including monitoring vital signs and providing symptomatic treatment as necessary. In cases of significant overdose, consultation with a poison control center or a medical toxicologist is recommended to guide further management.

It is crucial for healthcare professionals to educate patients about the importance of adhering to prescribed dosages and to provide clear instructions on what to do in the event of a suspected overdose.

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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this 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 attention 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 in a configuration that requires the removal of the safety tab prior to use. It should be stored at a temperature range of 68° to 77° F (20° to 25° C) to ensure optimal stability and efficacy. Proper handling and adherence to these storage conditions are essential for maintaining the integrity 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 intercourse or as directed by a healthcare professional. 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 Popstar, 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 Popstar, 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.