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Benzocaine

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This product has been discontinued

Active ingredient
Benzocaine 0.12 mL
Other brand names
Dosage form
Swab
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2011
Label revision date
March 22, 2011
Active ingredient
Benzocaine 0.12 mL
Other brand names
Dosage form
Swab
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2011
Label revision date
March 22, 2011
Manufacturer
Dynarex Corporation
Registration number
part348
NDC root
67777-235

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If you are a consumer or patient please visit this version.

Drug Overview

Benzocaine is a topical medication commonly found in products like Sting and Bite Pads. It is used for the temporary relief of pain and itching caused by minor burns, scrapes, and insect bites. By numbing the affected area, benzocaine helps to alleviate discomfort, allowing you to feel more at ease while your skin heals.

Uses

You can use this medication for temporary relief of pain and itching caused by minor burns, scrapes, and insect bites. It helps soothe discomfort and allows you to feel more comfortable while your skin heals.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for use.

Dosage and Administration

If you or your child is 2 years old or older and need to use this medication, you should apply it to the affected area three to four times a day. Make sure to follow this schedule consistently for the best results.

If your child is under 2 years old, it’s important to consult a physician (doctor) before using the medication. They can provide guidance on the appropriate treatment for younger children.

What to Avoid

It's important to be aware of certain precautions when using this medication. You should not use it during electrocautery procedures, which involve using electrical currents for surgical purposes. Additionally, avoid using this medication in or around your eyes, as it is not safe for that area.

Currently, there are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. Always follow these guidelines to ensure your safety and the effectiveness of your treatment.

Side Effects

When using this product, it's important to remember that it is for external use only and is flammable, so keep it away from fire or flames. You should stop using it if you experience any irritation or redness. If these symptoms persist for more than 72 hours, please consult a physician for further advice.

Warnings and Precautions

This product is for external use only, so please avoid using it on any internal areas. It is also flammable, so keep it away from fire or flames to ensure your safety.

If you accidentally swallow this product, seek emergency medical help or contact a Poison Control Center immediately. You should also stop using the product and call your doctor if you experience any irritation or redness, or if your condition does not improve after 72 hours. Your health and safety are important, so please take these precautions seriously.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that there is no specific information available about the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or special precautions have not been clearly outlined.

Before taking any medication, including this one, you should consult with your healthcare provider to discuss potential risks and benefits. They can help you make informed decisions that prioritize your health and the health of your baby.

Lactation Use

Currently, there is no information available regarding the use of Benzocaine while breastfeeding. This means that it’s unclear how this medication may affect you or your nursing infant. If you are considering using Benzocaine and are breastfeeding, it’s important to consult with your healthcare provider to discuss any potential risks and to explore safer alternatives if necessary. Always prioritize your health and the well-being of your baby when making decisions about medications.

Pediatric Use

If your child is under 2 years old, it's important to consult a physician (doctor) before using this medication. For children aged 2 years and older, you can apply the medication to the affected area 3 to 4 times a day. Always follow the recommended guidelines to ensure your child's safety and well-being.

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 considering this medication, it’s important to consult with a healthcare provider. 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 know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations for the medication do not change based on renal impairment. However, it’s always a good idea to discuss your kidney health with your healthcare provider, as they can offer personalized advice and monitor your condition effectively.

Make sure to keep them informed about any changes in your kidney function, as they may need to adjust your treatment plan accordingly. Your safety and well-being are the top priority, so regular check-ups and open communication with your doctor are essential.

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 differently due to your liver health.

It's always best to discuss your liver condition with your healthcare provider before starting any new medication. They can provide personalized advice and ensure that your treatment is safe and effective for you.

Drug Interactions

It's important to be aware of how certain procedures and medications can interact with each other. For instance, you should avoid using this medication during electrocautery procedures, which are surgical techniques that use electrical currents to cut tissue or control bleeding. This is crucial to ensure your safety and the effectiveness of your treatment.

While there are no specific laboratory test interactions noted, it's always a good idea to discuss any medications you are taking with your healthcare provider. They can help you understand potential interactions and ensure that your overall treatment plan is safe and effective. Always keep an open line of communication about your medications and any upcoming procedures.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, ideally between 15 to 30 degrees Celsius (59 to 86 degrees Fahrenheit). It's important to keep it away from excessive heat, as high temperatures can affect its quality and effectiveness.

When handling the product, always do so with care to maintain its integrity. Make sure to follow any specific instructions provided for use and disposal to ensure safety and effectiveness.

Additional Information

You should apply this medication topically to the affected area 3 to 4 times a day if you are an adult or a child aged 2 years and older. If the patient is under 2 years old, it's important to consult a physician before use. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is Benzocaine used for?

Benzocaine is used for temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.

How should I apply Benzocaine?

Adults and children 2 years of age and older should apply it to the affected area 3-4 times daily. For children under 2 years, consult a physician.

Are there any contraindications for using Benzocaine?

There are no contraindications listed for Benzocaine.

What precautions should I take when using Benzocaine?

Benzocaine is for external use only and is flammable, so keep it away from fire or flame.

What should I do if I experience irritation or redness?

Stop using Benzocaine if irritation and redness develop, and consult a physician if the condition persists for more than 72 hours.

What should I do if Benzocaine is swallowed?

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

Can I use Benzocaine with electrocautery procedures?

No, do not use Benzocaine with electrocautery procedures.

Is Benzocaine safe to use during pregnancy?

No specific information regarding the use of Benzocaine during pregnancy is provided.

How should I store Benzocaine?

Store Benzocaine at room temperature between 15 - 30 degrees C (59 - 86 degrees F) and avoid excessive heat.

Packaging Info

Below are the non-prescription pack sizes of Benzocaine. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Benzocaine.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The Sting and Bite Pad contains benzocaine as its active ingredient. Benzocaine is a local anesthetic that provides temporary relief from pain and discomfort associated with insect bites and stings. The formulation is designed for topical application, allowing for localized action at the site of irritation.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor burns, scrapes, and insect bites.

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

Dosage and Administration

For adults and children aged 2 years and older, the recommended application is to the affected area 3 to 4 times daily. The product should be applied gently and evenly to ensure adequate coverage of the affected skin.

For children under 2 years of age, it is advised to consult a physician prior to use to determine the appropriate course of action.

Contraindications

Use is contraindicated in the following situations:

Electrocautery procedures: Due to the potential for adverse interactions, the product should not be used in conjunction with electrocautery.

Ocular use: The product is contraindicated for application in the eyes, as it may cause harm or irritation.

Warnings and Precautions

For external use only. This product is flammable; therefore, it should be kept away from fire or flame to prevent any risk of ignition.

In the event of accidental ingestion, it is imperative to seek emergency medical assistance or contact a Poison Control Center immediately.

Users should discontinue use and consult a physician if any irritation or redness occurs. Additionally, if the condition persists for more than 72 hours, it is advised to stop using the product and seek medical advice.

Side Effects

Patients should be aware that the product is for external use only and is flammable; it should be kept away from fire or flame.

In clinical use, if irritation or redness develops, patients are advised to discontinue use immediately. Should these symptoms persist for more than 72 hours, it is recommended that patients consult a physician for further evaluation and management.

Drug Interactions

The use of this drug is contraindicated during electrocautery procedures due to the potential for adverse interactions. It is essential to avoid concurrent use to prevent complications associated with electrocautery.

There are no specific laboratory test interactions identified for this drug. Therefore, routine laboratory monitoring does not require any adjustments or special considerations related to this medication.

Packaging & NDC

Below are the non-prescription pack sizes of Benzocaine. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Benzocaine.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a physician prior to use. For children aged 2 years and older, the recommended application is to the affected area 3-4 times daily.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

There is no specific information regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in the absence of established safety profiles. Women of childbearing potential should be counseled on the importance of effective contraception during treatment.

Lactation

There is no information available regarding the use of Benzocaine in lactating mothers or its effects on breastfed infants. Healthcare professionals should consider this lack of data when advising lactating patients.

Renal Impairment

There is no information provided 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 absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from excessive dosing. Symptoms of overdosage can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, consultation with a poison control center or a medical toxicologist is recommended to guide further management and intervention strategies.

Documentation of the incident, including the amount ingested and the time of exposure, is crucial for effective treatment and follow-up care.

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. It is important to emphasize that if the medication is swallowed, patients should seek medical help immediately or contact a Poison Control Center for assistance. This guidance is crucial to ensure the safety and well-being of patients and to mitigate any potential risks associated with accidental ingestion.

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 room temperature, maintaining a range of 15 to 30 degrees Celsius (59 to 86 degrees Fahrenheit). Care should be taken to avoid exposure to excessive heat, as this may compromise the integrity of the product. Proper storage conditions are crucial to ensure the product's efficacy and safety.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3-4 times daily for adults and children aged 2 years and older. For children under 2 years of age, it is advised to consult a physician prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for 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 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.

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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.