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Cvs Oral Anesthetic

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This product has been discontinued

Active ingredient
Benzocaine 200 mg/1 mL
Other brand names
Dosage form
Liquid
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2010
Label revision date
July 8, 2010
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 200 mg/1 mL
Other brand names
Dosage form
Liquid
Route
Oral
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 2010
Label revision date
July 8, 2010
Manufacturer
CVS Pharmacy
Registration number
part356
NDC root
59779-186
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

This medication is designed to provide temporary relief from pain associated with various mouth and gum irritations. You may find it helpful for conditions such as toothaches, canker sores, sore gums, and discomfort caused by braces or dentures. It can also be used after minor dental procedures to ease any pain you might experience.

By targeting the source of discomfort, this medication helps to soothe your mouth and gums, allowing you to feel more comfortable during your daily activities. If you're dealing with any of these issues, this product may be a supportive option for you.

Uses

You can use this medication to temporarily relieve pain caused by various mouth and gum irritations. This includes discomfort from toothaches, canker sores, sore gums, and issues related to braces or dentures. It can also help ease pain following minor dental procedures.

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 those concerned about such risks.

Dosage and Administration

When using this medication, you should apply it directly to the affected area. For adults and children aged 2 years and older, you can use a cotton ball, cotton swab, or your fingertip to wipe the liquid onto the skin. You can apply it up to four times a day, or as directed by your doctor or dentist.

If you are using this product for children under 12 years old, make sure an adult supervises the application. For children younger than 2 years, it’s important to consult with a dentist or doctor before use to ensure safety and proper guidance.

What to Avoid

It's important to be cautious when using this medication. If you accidentally swallow more than the recommended amount for pain relief, seek medical help immediately or contact a Poison Control Center. This ensures your safety and well-being.

Currently, there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with this medication. However, always use it as directed to avoid any potential risks.

Side Effects

If you have a history of allergies to local anesthetics like procaine, butacaine, or benzocaine, you should not use this product. While using it, be careful to avoid contact with your eyes, and do not exceed the recommended dosage or use it for more than 7 days unless directed by a healthcare professional.

You should stop using the product and consult a dentist or doctor if your sore mouth symptoms do not improve within 7 days, or if you experience swelling, a rash, fever, or if irritation, pain, or redness persists or worsens.

Warnings and Precautions

You should avoid using this product if you have ever had an allergic reaction to local anesthetics, such as procaine, butacaine, or benzocaine. While using the product, be careful not to let it come into contact with your eyes, and make sure not to exceed the recommended dosage. It's also important not to use it for more than 7 days unless your doctor or dentist advises you to do so.

If your sore mouth symptoms do not improve after 7 days, or if you experience swelling, a rash, or fever, you should stop using the product and consult your dentist or doctor. Additionally, if you notice any irritation, pain, or redness that persists or worsens, seek medical advice. In case you accidentally swallow more than the recommended amount, get emergency medical help or contact a Poison Control Center immediately.

Overdose

If you accidentally take more than the recommended dosage of this medication, it’s important to seek medical help immediately or contact a Poison Control Center. Overdosing can lead to serious health issues, so don’t hesitate to reach out for assistance.

Signs of an overdose may include unusual symptoms that could affect your breathing or overall well-being. If you notice any concerning changes in your health after taking the medication, it’s crucial to get help right away. Always prioritize your safety and well-being by being aware of the proper dosage and what to do in case of an emergency.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of benzocaine, a common topical anesthetic, has not been established. Due to potential risks to the fetus, benzocaine is generally not recommended for use during pregnancy.

Before using any product containing benzocaine, you should consult your healthcare provider to discuss your specific situation and any potential risks. Your health and the health of your baby are the top priority, so seeking professional advice is essential.

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. Additionally, there are no known concerns about the product being passed into breast milk or any associated risks for your infant. This means you can use the product without worrying about its effects on your milk production or your baby's health.

Pediatric Use

When using this product for children, it's important to follow specific guidelines to ensure their safety. For children aged 2 years and older, you can apply the product directly to the affected area. However, if your child is under 12 years old, make sure they are supervised by an adult during use.

If your child is under 2 years old, it's crucial to consult a dentist or doctor before using the product. This will help ensure that it is safe and appropriate for their age and health needs. Always prioritize your child's safety and well-being when using any medical product.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it's important to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances. Always prioritize open communication with your doctor 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 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 and what steps to take for your safety.

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 detailed guidelines available regarding how the medication may affect you or how your liver health might influence the treatment.

Before starting any new medication, it's essential to discuss your liver condition with your healthcare provider. They can help determine the best approach for your treatment and ensure that your liver health is taken into account. Always keep your doctor informed about any changes in your health or any concerns you may have.

Drug Interactions

It's important to be aware of potential interactions when considering any medication. If you have a history of allergies to local anesthetics, such as procaine, butacaine, benzocaine, or other "caine" anesthetics, you should avoid using this product. Allergic reactions can be serious, so discussing your medical history with your healthcare provider is crucial.

Additionally, while there are no specific interactions with other drugs or laboratory tests noted, it's always a good practice to inform your healthcare provider about all medications and tests you are undergoing. This ensures your safety and helps your provider make the best decisions for your health.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature, away from direct light. It's important to keep the container tightly closed when not in use to prevent contamination. Once you open the container, please remember to discard it after use to maintain safety and effectiveness. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You can use this medication by applying it orally to the affected area. For adults and children aged 2 years and older, you should wipe the liquid on using a cotton ball, cotton swab, or your fingertip. You can apply it up to four times a day or as directed by your doctor or dentist. If you are using it for children under 12, make sure an adult supervises the application. For children under 2 years old, it's important to consult a dentist or doctor before use.

FAQ

What is the primary use of this drug?

This drug temporarily relieves pain associated with mouth and gum irritations, including toothache, canker sores, sore gums, braces, dentures, and minor dental procedures.

Who can use this product?

Adults and children 2 years of age and older can use this product. Children under 12 should be supervised by an adult, and those under 2 years should consult a dentist or doctor.

How should I apply this product?

You should apply the liquid to the affected area using a cotton swab, cotton, or your fingertip, up to 4 times daily or as recommended by a doctor or dentist.

Are there any allergies I should be aware of?

Do not use this product if you have a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other 'caine' anesthetics.

What should I do if I accidentally swallow more than the recommended amount?

If more than the recommended amount is swallowed, seek medical help or contact a Poison Control Center immediately.

What precautions should I take while using this product?

Avoid contact with eyes, do not exceed the recommended dosage, and do not use for more than 7 days unless directed by a doctor or dentist.

What should I do if my symptoms do not improve?

If sore mouth symptoms do not improve in 7 days, or if swelling, rash, or fever develops, stop use and consult a dentist or doctor.

Is this product safe to use during pregnancy?

The safety of this product during pregnancy has not been established, and it is contraindicated due to potential risks to the fetus. Consult a healthcare provider if pregnant or planning to become pregnant.

How should I store this product?

Store at room temperature, protect from light, keep the container tightly closed, and discard after opening.

Packaging Info

Below are the non-prescription pack sizes of Cvs Oral Anesthetic (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Oral Anesthetic.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The drug is formulated as a tablet containing the active ingredient insert active ingredient name here. The tablet is characterized by its insert color, shape, and any other physical characteristics here. Inactive ingredients include list of inactive ingredients here.

Uses and Indications

This drug is indicated for the temporary relief of pain associated with various mouth and gum irritations, including toothache, canker sores, sore gums, discomfort from braces, irritation from dentures, and pain resulting from minor dental procedures.

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

Dosage and Administration

For adults and children aged 2 years and older, the product should be applied directly to the affected area. The liquid formulation can be administered using a cotton ball, cotton swab, or fingertip. The recommended application frequency is up to four times daily, or as directed by a healthcare professional.

For children under 12 years of age, adult supervision is required during the use of this product to ensure safe and effective application. In the case of children under 2 years of age, it is essential to consult a dentist or physician prior to use to determine the appropriateness of treatment.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if an overdose occurs, defined as the accidental ingestion of more than the recommended dosage for pain relief.

Warnings and Precautions

The use of this product is contraindicated in individuals with a known allergy to local anesthetics, including but not limited to procaine, butacaine, benzocaine, or any other "caine" anesthetics.

When administering this product, it is imperative to avoid contact with the eyes. Healthcare professionals should advise patients not to exceed the recommended dosage and to limit use to a maximum of 7 days unless otherwise directed by a qualified healthcare provider, such as a doctor or dentist.

Patients should be instructed to discontinue use and seek advice from a dentist or doctor if any of the following occur: sore mouth symptoms do not improve within 7 days; the development of swelling, rash, or fever; or if irritation, pain, or redness persists or worsens.

In cases where more than the recommended amount has been ingested, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Side Effects

Patients should be aware of the potential adverse reactions associated with this product. A significant warning is that individuals with a history of allergy to local anesthetics, including procaine, butacaine, benzocaine, or other "caine" anesthetics, should not use this product.

During the use of this product, patients are advised to avoid contact with the eyes and to adhere strictly to the recommended dosage. It is also important to note that the product should not be used for more than 7 days unless directed by a healthcare professional.

Patients should discontinue use and consult a dentist or doctor if sore mouth symptoms do not improve within 7 days. Additionally, they should seek medical advice if they experience swelling, rash, or fever, or if irritation, pain, or redness persists or worsens. These precautions are essential to ensure patient safety and to mitigate the risk of serious adverse reactions.

Drug Interactions

Patients with a known history of allergy to local anesthetics, including procaine, butacaine, benzocaine, or other "caine" anesthetics, should not use this product due to the potential for severe allergic reactions.

No specific drug or laboratory test interactions have been identified in the available data. Therefore, routine monitoring or dosage adjustments related to drug interactions are not necessary.

Packaging & NDC

Below are the non-prescription pack sizes of Cvs Oral Anesthetic (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cvs Oral Anesthetic.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the product to the affected area as directed. For children under 12 years of age, adult supervision is recommended during the use of this product to ensure safety and proper application. In pediatric patients under 2 years of age, it is advised to consult a dentist or doctor prior to use to assess appropriateness and safety.

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

The safety of benzocaine during pregnancy has not been established. Benzocaine is contraindicated in pregnancy due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a healthcare provider before using this product to discuss potential risks and benefits.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there are no statements concerning the potential for excretion in breast milk or any associated risks to breastfed infants during lactation.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the text. Therefore, healthcare professionals should exercise caution and consider individual patient factors when prescribing to patients with reduced kidney function. Regular monitoring of renal function may be warranted in these patients, although specific guidelines are not outlined.

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 assistance is crucial. If a patient accidentally ingests more than the recommended dosage, it is imperative to seek medical help or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt intervention can significantly mitigate potential adverse effects associated with overdosage. Monitoring the patient for any symptoms that may arise is essential, although specific symptoms related to overdosage are not detailed in the provided information.

Management of overdosage should be guided by clinical judgment and may involve supportive care and symptomatic treatment as necessary. It is advisable to follow established protocols for the management of overdose cases, ensuring that the patient receives appropriate care based on their clinical presentation.

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 understanding of potential risks associated with the compound in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

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 misuse. In the event that a patient accidentally swallows more than the recommended dose for pain relief, they should seek medical assistance or contact a Poison Control Center immediately. This information is crucial for ensuring patient safety and promoting responsible use of the medication.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light exposure to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The product is administered orally, with application directed to the affected area. For adults and children aged 2 years and older, the liquid should be wiped on using a cotton ball, cotton swab, or fingertip, with a maximum frequency of up to four times daily or as directed by a healthcare professional. It is advised that children under 12 years of age use the product under adult supervision, while consultation with a dentist or doctor is recommended for children under 2 years of age.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Cvs Oral Anesthetic, 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 Cvs Oral Anesthetic, 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.