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Body Action Products Butt Eze Benzocaine

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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
November 10, 2023
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
November 10, 2023
Manufacturer
PRODUCT MAX GROUP INC
Registration number
M015
NDC root
70742-286
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

You can use this medication for temporary relief of pain or soreness in the perianal area, which is the area around the anus. It is designed to help ease discomfort, allowing you to feel more comfortable during daily activities. If you're experiencing pain in this area, this medication may provide the relief you need.

Uses

If you're experiencing pain or soreness in the perianal area, this medication can provide temporary relief. It's designed to help ease discomfort, allowing you to feel more comfortable in your daily activities. Always consult with a healthcare professional if you have any questions or concerns about your symptoms.

Dosage and Administration

To use this product effectively, start by cleaning the affected area with mild soap and warm water. Make sure to rinse it thoroughly to remove any soap residue. After cleansing, gently dry the area by patting or blotting it with toilet tissue or a soft cloth.

Once the area is dry, you can apply the product. You can use it up to six times a day, depending on your needs. Just remember to follow these steps each time for the best results.

What to Avoid

It's important to be aware of certain precautions when using this medication. While there are no specific contraindications or concerns about abuse, misuse, or dependence (which means relying on a substance in a harmful way), you should take care to follow the instructions provided.

If you accidentally swallow the medication, seek medical help immediately or contact a Poison Control Center. Your safety is the top priority, so please ensure you handle the medication responsibly.

Side Effects

This product is intended for external use only, so be sure to avoid contact with your eyes. Some individuals may experience allergic reactions to the ingredients. If you notice that the symptoms you are treating do not improve, or if you develop redness, irritation, swelling, pain, or any other worsening symptoms, it’s important to stop using the product and consult a doctor.

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to your eyes. Some individuals may experience allergic reactions to the ingredients. If you notice that the symptoms you are treating do not improve, or if you develop redness, irritation, swelling, pain, or any other concerning symptoms, stop using the product and consult your doctor.

In case of accidental ingestion, seek medical help immediately or contact a Poison Control Center. Your safety is important, so please take these precautions seriously.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to reach out for help. Remember, acting quickly can make a significant difference in ensuring safety and health.

Pregnancy Use

It’s important to note that there is currently no information available about the use of Butt Eze Benzocaine Gel during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been established. If you are pregnant or planning to become pregnant, it’s best to consult with your healthcare provider before using this product to ensure your safety and the safety of your baby.

Lactation Use

If you are a nursing mother, you can use Butt Eze Benzocaine Gel without specific warnings or recommendations against its use. Currently, there is no information available about whether this product is passed into breast milk or if it poses any risk to your infant.

As always, it's a good idea to consult with your healthcare provider if you have any concerns about using new products while breastfeeding. They can provide personalized advice based on your situation.

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 considering the use of Butt Eze Benzocaine Gel for older adults, it's important to note that the drug insert does not provide specific information about how this product may affect elderly patients. This means there are no special dosage adjustments, safety concerns, or precautions outlined for older individuals.

If you are caring for an older adult, it’s always a good idea to consult with a healthcare professional before starting any new medication, including over-the-counter products like this gel. They can help ensure that it is safe and appropriate based on individual health needs.

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 medication or 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 there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard dosing may apply to you, but it’s always best to consult with your healthcare provider for personalized advice. They can help monitor your liver function and ensure that any medications you take are safe and effective for you. Always keep your doctor informed about your liver health to receive the best care possible.

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 use of your product, store it at room temperature. This helps maintain its effectiveness and safety. Before using, always check that the safety seal is intact; do not use the product if the seal is broken or missing, as this could indicate that it is no longer safe to use. Following these simple guidelines will help you handle the product safely and effectively.

Additional Information

You should apply the medication to the affected area up to six times a day for optimal results. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling information.

FAQ

What is the purpose of this drug?

This drug is used for temporary relief of pain or soreness in the perianal area.

How should I apply this product?

Cleanse the affected area with mild soap and warm water, then gently dry it. Apply the product to the affected area up to 6 times daily.

Are there any warnings I should be aware of?

Yes, this product is for external use only, avoid contact with the eyes, and discontinue use if you experience redness, irritation, or other symptoms.

What should I do if I swallow this product?

If swallowed, get medical help or contact a Poison Control Center right away.

Is there any information about using this product during pregnancy?

There is no information provided regarding the use of this product during pregnancy.

Can nursing mothers use this product?

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

How should I store this product?

Store at room temperature and do not use if the safety seal is broken or missing.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

What should I do if I experience an allergic reaction?

If you develop an allergic reaction or if symptoms do not subside, discontinue use and consult a doctor.

Packaging Info

Below are the non-prescription pack sizes of Body Action Products Butt Eze Benzocaine (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Body Action Products Butt Eze Benzocaine.
Details

Drug Information (PDF)

This file contains official product information for Body Action Products Butt Eze Benzocaine, 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 additional specific description details are provided in the available data.

Uses and Indications

This drug is indicated for the temporary relief of pain or soreness in the perianal area.

Dosage and Administration

When practical, the affected area should be cleansed with mild soap and warm water, followed by thorough rinsing. After cleansing, the area must be gently dried by patting or blotting with toilet tissue or a soft cloth prior to the application of the product. The product may be applied to the affected area up to 6 times daily, ensuring that the application is performed with care to maximize efficacy and minimize irritation.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that if the product is swallowed, medical assistance should be sought immediately or contact a Poison Control Center.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes to prevent irritation or injury.

Allergic reactions may occur in certain individuals due to the ingredients in this product. Should the symptom being treated not improve, or if any adverse reactions such as redness, irritation, swelling, or pain develop or worsen, it is essential to discontinue use immediately and consult a healthcare professional.

In the event of accidental ingestion, seek medical assistance or contact a Poison Control Center without delay.

Side Effects

Patients using this product should be aware that it is intended for external use only and must avoid contact with the eyes. There is a potential for allergic reactions to the ingredients contained in the formulation. In clinical observations, certain individuals have reported developing allergic reactions, which may manifest as redness, irritation, swelling, pain, or other symptoms.

If the symptom being treated does not subside, or if any of the aforementioned symptoms develop or worsen, patients are advised to discontinue use immediately and consult a healthcare professional for further evaluation and guidance.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. 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 Body Action Products Butt Eze Benzocaine (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Body Action Products Butt Eze Benzocaine.
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

Elderly patients may not have specific information regarding the use of Butt Eze Benzocaine Gel, as the drug insert does not provide details on dosage adjustments, safety concerns, or special precautions for this population. Healthcare providers should exercise caution when prescribing this medication to geriatric patients, considering the absence of data that may inform its safety and efficacy in this age group. Monitoring for potential adverse effects is advisable, given the lack of targeted studies or recommendations for elderly patients.

Pregnancy

There is currently no information available regarding the use of Butt Eze Benzocaine Gel during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals should exercise caution when considering the use of this product in pregnant patients due to the lack of data on potential risks or fetal outcomes. Women of childbearing potential should be advised to consult their healthcare provider before using this product during pregnancy.

Lactation

There are no specific warnings or recommendations regarding the use of Butt Eze Benzocaine Gel 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 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

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise clinical judgment when considering the use of this medication in patients with liver problems, as the absence of specific guidance necessitates careful evaluation of the patient's overall health status and liver function.

Overdosage

In the event of an overdosage, immediate medical assistance is crucial. Healthcare professionals are advised to seek medical help or contact a Poison Control Center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved. It is essential for healthcare providers to assess the patient’s condition thoroughly and monitor for any adverse effects that may arise.

Management of overdosage should be guided by the clinical presentation and the specific characteristics of the substance. Supportive care and symptomatic treatment are often necessary. In cases of ingestion, activated charcoal may be considered if appropriate and within the recommended time frame, depending on the substance and the patient's clinical status.

Prompt intervention and appropriate management strategies are critical in mitigating the effects of an overdosage and ensuring patient safety.

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 medication is swallowed, it is crucial to seek medical help or contact a Poison Control Center immediately. This information is essential for ensuring patient safety and prompt action in case of accidental ingestion.

Storage and Handling

The product is supplied in configurations that include specific NDC numbers. It should be stored at room temperature to maintain its integrity and efficacy. Healthcare professionals are advised to ensure that the safety seal is intact before use; the product should not be utilized if the safety seal is broken or missing. Proper handling and storage conditions are essential to ensure the product remains safe and effective for patient use.

Additional Clinical Information

Patients should apply the medication to the affected area up to six times daily. 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 Body Action Products Butt Eze Benzocaine, 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 Body Action Products Butt Eze Benzocaine, 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.