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A and E Deep Throat Desensitizing Spraystrawberry

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Active ingredient
Benzocaine 3 mg/100 mL
Other brand names
Drug class
Standardized Chemical Allergen
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
November 11, 2025
Active ingredient
Benzocaine 3 mg/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
Marketed in the U.S.
Since 2025
Label revision date
November 11, 2025
Manufacturer
Phe Inc
Registration number
M017
NDC root
87068-183

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Drug Overview

This medication is designed for occasional personal use to help prevent the gag reflex, which can be helpful in various situations, such as during medical examinations or certain procedures. It works by reducing the sensitivity of the throat, making it easier for you to undergo activities that might otherwise trigger discomfort or a gagging response.

If you find yourself needing assistance with this reflex, this medication may provide the support you need to feel more comfortable. Always consult with a healthcare professional to ensure it’s appropriate for your specific situation.

Uses

You can use this medication occasionally to help prevent the gag reflex, which can be helpful in certain situations. It's important to note that there are no reported teratogenic effects (harmful effects on fetal development) associated with this medication, so it is considered safe in that regard. Additionally, there are no nonteratogenic effects (effects that do not harm fetal development) mentioned, making it a straightforward option for its intended use.

Dosage and Administration

When using this medication, you should apply 2 to 3 sprays directly to the back of your throat. It's important to limit your use to no more than 3 to 4 times a day to ensure safety and effectiveness. Please remember that this medication is intended for adults aged 18 years and older, so it should not be used by anyone younger than that.

What to Avoid

It's important to keep this medication out of reach of children to prevent any accidental ingestion. If an overdose occurs or if the medication is ingested by someone it wasn't prescribed for, please contact a Poison Control Center immediately for assistance.

While there are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication, always use it responsibly and as directed by your healthcare provider.

Side Effects

Using this product may lead to a serious condition called methemoglobinemia, which reduces the amount of oxygen in your blood. This can happen even if you have used the product before. If you or a child experiences symptoms such as pale, gray, or blue skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness, or fatigue, it is important to stop using the product and seek immediate medical attention.

Warnings and Precautions

Using this product may lead to a serious condition called methemoglobinemia, which reduces the amount of oxygen in your blood. This can happen even if you have used the product before. If you or a child in your care experiences symptoms such as pale, gray, or blue skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness, or fatigue, stop using the product immediately and seek emergency medical help.

It's crucial to be aware of these symptoms and act quickly. If you notice any of these signs, do not hesitate to stop using the product and contact your doctor right away. Your health and safety are the top priority, so please take these warnings seriously.

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 that you or someone else may have taken too much of a medication, it’s crucial to seek immediate medical help.

In case of an overdose, contact your local emergency services or go to the nearest hospital. Having the medication packaging or information on hand can help medical professionals provide the best care. Always remember that when it comes to medications, it’s better to be safe and get help if you have any concerns.

Pregnancy Use

When it comes to using this medication during pregnancy, there are no specific guidelines or safety concerns mentioned. This means that the information available does not provide clear recommendations or precautions for pregnant individuals or those planning to become pregnant.

If you are pregnant or considering pregnancy, it's always best to consult with your healthcare provider before starting any new medication. They can help you understand any potential risks and make informed decisions that are right for you and your baby.

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. Currently, there is also no information available about whether this product is excreted in breast milk or any potential risks to your infant.

As always, it's a good idea to consult with your healthcare provider if you have any concerns or questions about using this product while breastfeeding. Your health and the health of your baby are important, and your provider can help you make informed decisions.

Pediatric Use

It's important to keep this medication out of reach of children to ensure their safety. If you notice any concerning symptoms in your child, such as pale, gray, or blue skin (known as cyanosis), headache, rapid heart rate, shortness of breath, dizziness, or unusual fatigue, stop using the medication immediately and seek medical help.

This medication is intended for adults only and should not be given to minors. Always prioritize safety and consult with a healthcare professional if you have any questions or concerns regarding its use.

Geriatric Use

When it comes to using this medication in older adults, there are no specific guidelines or dosage adjustments mentioned. This means that, as an older adult or caregiver, you should be aware that the usual safety concerns and precautions that apply to younger patients may also apply here. It's always a good idea to discuss any potential risks or side effects with your healthcare provider, especially if you have other health conditions or are taking multiple medications.

If you have any questions or concerns about how this medication may affect you or your loved one, don't hesitate to reach out to a healthcare professional for personalized advice.

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 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 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 your overall treatment plan is safe and effective. Always share your complete list of medications and any health concerns to receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it at a temperature between 20-25°C (68-77°F). This temperature range helps maintain its effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a clean environment to avoid contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal.

Additional Information

You should apply this medication topically by spraying 2–3 times to the back of your throat. For adults aged 18 and older, it's important to limit your use to 3–4 times per day to ensure safe and effective treatment. There are no additional details regarding laboratory tests, abuse potential, or patient counseling information available at this time.

FAQ

What is this drug used for?

This drug is for occasional personal use to help prevent the gag reflex.

Who can use this drug?

This drug is for adults 18 years of age and older only and is not for sale to minors.

How should I use this drug?

You should apply 2–3 sprays to the back of the throat, limiting use to 3–4 times per day.

Are there any warnings associated with this drug?

Yes, the drug may cause methemoglobinemia, a serious condition that reduces oxygen in the blood. Seek immediate medical attention if you or a child develops symptoms like pale skin, headache, or shortness of breath.

What should I do if I experience serious side effects?

Stop using the drug and seek immediate medical attention if you or a child develops symptoms such as cyanosis, headache, rapid heart rate, or dizziness.

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

There is no specific information provided regarding the use of this drug during pregnancy or lactation.

How should I store this drug?

Store the drug at 20-25°C (68-77°F).

What precautions should I take with this drug?

Keep the drug out of reach of children and contact a Poison Control Center in case of accidental overdose or ingestion.

Packaging Info

Below are the non-prescription pack sizes of A and E Deep Throat Desensitizing Spraystrawberry (oral numbing spray strawberry). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for A and E Deep Throat Desensitizing Spraystrawberry.
Details

Drug Information (PDF)

This file contains official product information for A and E Deep Throat Desensitizing Spraystrawberry, 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 occasional personal use to help prevent the gag reflex.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

For adults aged 18 years and older, the recommended dosage is to apply 2 to 3 sprays directly to the back of the throat. Administration should be limited to a maximum of 3 to 4 times per day. This product is intended for adult use only and is not approved for sale to minors.

Contraindications

There are no specific contraindications listed for this product. However, it is essential to keep the product out of reach of children to prevent accidental ingestion. In the event of an accidental overdose or ingestion, it is advised to contact a Poison Control Center immediately for assistance.

Warnings and Precautions

The use of this product carries a significant risk of methemoglobinemia, a serious condition characterized by reduced oxygen transport in the blood. Healthcare professionals should be vigilant, as methemoglobinemia can occur even in patients who have previously used this product without incident. Immediate cessation of use and prompt medical evaluation are imperative if any of the following symptoms develop in the patient or a child under their care:

  • Cyanosis, indicated by pale, gray, or blue-colored skin

  • Headache

  • Rapid heart rate

  • Shortness of breath

  • Dizziness or lightheadedness

  • Fatigue or lack of energy

In the event that any of these symptoms manifest, it is crucial to seek emergency medical assistance without delay. The healthcare provider should ensure that patients are aware of these potential adverse effects and the importance of monitoring for them during treatment.

Side Effects

The use of this product may lead to methemoglobinemia, a serious condition characterized by reduced oxygen transport in the blood. This adverse reaction can occur even in patients who have previously used the product without incident. It is crucial for patients and caregivers to be vigilant for symptoms indicative of methemoglobinemia, which include pale, gray, or blue-colored skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness or lightheadedness, and fatigue or lack of energy. In the event that any of these symptoms develop, immediate medical attention should be sought to ensure prompt treatment.

Drug Interactions

There are currently no documented drug interactions associated with the use of 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 A and E Deep Throat Desensitizing Spraystrawberry (oral numbing spray strawberry). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for A and E Deep Throat Desensitizing Spraystrawberry.
Details

Pediatric Use

Pediatric patients should not have access to this medication, and it must be kept out of reach of children. The use of this medication is contraindicated in individuals under the age of 18, as it is intended for adults only.

Healthcare professionals should advise caregivers to stop use and seek immediate medical attention if a child develops symptoms such as pale, gray, or blue-colored skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness or lightheadedness, or fatigue or lack of energy.

Geriatric Use

Elderly patients may not have specific information available 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 be aware that there is no specific information regarding the use of this medication during pregnancy. Safety concerns related to fetal outcomes have not been specified, and there are no known dosage modifications or special precautions indicated for pregnant individuals. Healthcare professionals are advised to consider the lack of data when prescribing this medication to women of childbearing potential and to weigh the potential risks and benefits.

Lactation

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

Renal Impairment

There is no specific information regarding renal impairment, dosage adjustments, special monitoring, or safety considerations for patients with reduced kidney function. Healthcare professionals should exercise caution and consider individual patient factors when treating patients with renal impairment, as the absence of detailed guidance necessitates careful clinical judgment.

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 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 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 a suspected overdose, immediate medical evaluation is recommended. Healthcare professionals should assess the patient's vital signs and obtain a thorough history, including the substance involved, the amount taken, and the time of ingestion.

Management of an overdose typically involves supportive care, which may include airway management, intravenous fluids, and monitoring of vital signs. Specific antidotes or treatments may be indicated based on the substance involved, and consultation with a poison control center or toxicology expert is advisable for guidance on appropriate interventions.

It is crucial for healthcare professionals to document all findings and interventions thoroughly and to report any adverse events to the appropriate regulatory authorities as per local guidelines.

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 question. Further studies may be necessary to elucidate these aspects of nonclinical toxicology.

Postmarketing Experience

Postmarketing experience has identified the potential for methemoglobinemia associated with the use of this product. Methemoglobinemia is a serious condition that can significantly reduce the oxygen-carrying capacity of the blood and requires prompt medical intervention. Reports indicate that this condition may occur even in individuals who have previously used the product without incident.

Healthcare professionals are advised to instruct patients to discontinue use and seek immediate medical attention if symptoms such as pale, gray, or blue-colored skin (cyanosis), headache, rapid heart rate, shortness of breath, dizziness or lightheadedness, or fatigue or lack of energy develop.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important for patients to understand the potential risks associated with overdose or unintentional ingestion. In such cases, they should be instructed to contact a Poison Control Center immediately for guidance and assistance. This information is crucial for ensuring patient safety and promoting responsible use of the medication.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at a controlled temperature range of 20-25°C (68-77°F) to maintain its integrity and efficacy. Proper storage conditions should be ensured to prevent exposure to extreme temperatures, which may compromise the product's quality.

Additional Clinical Information

The product is administered topically, with a recommended application of 2–3 sprays to the back of the throat for adults aged 18 years and older. Clinicians should advise patients to limit the use to 3–4 times per day. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for A and E Deep Throat Desensitizing Spraystrawberry, 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 A and E Deep Throat Desensitizing Spraystrawberry, 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.

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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.