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Oral Analgesic

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This product has been discontinued

Active ingredient
Benzocaine 0.2 mL/1 mL
Other brand names
Dosage form
Liquid
Route
Topical
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
May 13, 2010
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 0.2 mL/1 mL
Other brand names
Dosage form
Liquid
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 2010
Label revision date
May 13, 2010
Manufacturer
Meijer Distribution Inc.
Registration number
part356
NDC root
41250-703
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

Meijer Oral Analgesic Liquid is a maximum strength oral pain relief medication that contains 20% benzocaine (a local anesthetic that numbs the area). It is designed to provide fast relief from oral pain caused by various issues, including toothaches, denture or gum irritations, and cold or canker sores.

This liquid formulation is easy to use and is packaged with a safety-sealed tube tip to ensure its integrity. If you're experiencing discomfort in your mouth, this product may help alleviate your pain effectively.

Uses

If you're experiencing oral pain, this medication can provide quick relief for several common issues. It is effective for toothaches, which can be quite uncomfortable, as well as for irritations caused by dentures or gums. Additionally, if you have cold sores or canker sores, this treatment can help ease the pain associated with those conditions.

You can feel confident using this medication, as there are no known teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects associated with it. This makes it a safe option for managing your oral discomfort.

Dosage and Administration

To use this product effectively, you should apply it directly to the affected area using a cotton swab or a clean fingertip. This topical (applied to the skin) medication can be used up to four times a day, or as your dentist or doctor advises.

If you are applying this product for a child under 12 years old, make sure they are supervised during use. For children younger than 2 years, it’s important to consult with a dentist or doctor before use to ensure safety. Always follow the guidance provided by your healthcare professional for the best results.

What to Avoid

It's important to use this medication responsibly to ensure your safety and well-being. You should not use it for more than 7 days unless your dentist or doctor specifically instructs you to do so. Always follow the dosage instructions carefully and avoid using more than directed. Additionally, be cautious to keep the medication away from your eyes, as contact can cause irritation or harm.

Side Effects

You should be aware of some important side effects and warnings associated with this product. If you have a history of allergies to local anesthetics like procaine, butacaine, or benzocaine, you should not use this product. It is also flammable, so keep it away from fire or flames and avoid smoking while using it.

While using this product, avoid contact with your eyes and do not exceed the recommended usage of more than 7 days unless directed by a dentist or doctor. If your sore mouth symptoms do not improve after 7 days, or if you experience persistent irritation, pain, or redness, you should stop using the product and consult a doctor. Additionally, seek medical help immediately if you notice swelling, a rash, fever, or suspect an overdose.

Warnings and Precautions

You should be aware of some important warnings and precautions when using this product. If you have a history of allergies to local anesthetics like procaine, butacaine, or benzocaine, do not use this product. Additionally, it is flammable, so keep it away from fire or flames, and avoid smoking while using it and until it has dried.

While using this product, be careful to avoid contact with your eyes, and do not use more than the recommended amount or for longer than 7 days unless directed by a dentist or doctor. If your sore mouth symptoms do not improve after 7 days, or if you experience worsening irritation, pain, redness, swelling, rash, or fever, stop using the product and contact your doctor. In case of an overdose, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

If you suspect an overdose, it’s crucial to seek medical help immediately or contact a Poison Control Center. Signs of an overdose can vary, but they may include unusual symptoms that are more severe than typical side effects.

Always err on the side of caution—if you or someone else is experiencing concerning symptoms after taking medication, don’t hesitate to reach out for professional assistance. Your health and safety are the top priority.

Pregnancy Use

When considering the use of Oral Analgesic Maximum Strength - benzocaine liquid during pregnancy, it's important to note that the drug insert does not provide specific information about its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that there is no clear guidance on whether it is safe to use during pregnancy.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before using any medication, including over-the-counter products like benzocaine. They can help you weigh the potential risks and benefits based on your individual health needs.

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. This means that, according to the information available, it is considered safe for you to use without concerns about potential effects on your milk production or the nursing infant.

Additionally, there are no indications that this product is excreted in breast milk, which further supports its use during lactation. Always consult with your healthcare provider if you have any questions or concerns about medications while breastfeeding.

Pediatric Use

When using this product for children, it's important to keep a few guidelines in mind. For children under 12 years old, you should supervise their use of the product to ensure safety. If your child is under 2 years old, it's best to consult with a dentist or doctor before use to get specific advice tailored to their needs.

For children aged 2 years and older, you can apply the product directly to the affected area using a cotton swab or a clean fingertip. This can be done up to four times a day or as directed by a healthcare professional. Always follow these recommendations to ensure the safe and effective use of the product for your child.

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 the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

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.

While there are no specific interactions with other drugs or laboratory tests mentioned, 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 them provide the best care tailored to your needs.

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 should apply this medication topically, which means you will be putting it directly on your skin. You can use it up to four times a day, or as your dentist or doctor advises. If you have any questions about how to use it or how often, be sure to consult with your healthcare provider for guidance.

FAQ

What is Meijer Oral Analgesic Liquid used for?

Meijer Oral Analgesic Liquid is used for fast relief of oral pain caused by toothache, denture or gum irritations, and cold or canker sores.

How should I use Meijer Oral Analgesic Liquid?

Apply the product with a cotton swab or clean fingertip to the affected area. You can use it up to 4 times daily or as directed by a dentist or doctor.

Are there any age restrictions for using this product?

Children under 12 years of age should be supervised while using this product, and for children under 2 years of age, you should ask a dentist or doctor.

What should I do if my symptoms do not improve?

Stop using the product and ask a doctor if sore mouth symptoms do not improve in 7 days, or if irritation, pain, or redness persists or worsens.

Are there any warnings associated with this product?

Yes, do not use this product if you have a history of allergy to local anesthetics like benzocaine. It is also flammable, so keep it away from fire or flame.

What should I do in case of overdose?

In case of overdose, get medical help or contact a Poison Control Center right away.

Can I use this product during pregnancy or while nursing?

There are no specific warnings or recommendations regarding the use of this product during pregnancy or lactation in the provided information.

How should I store Meijer Oral Analgesic Liquid?

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

Packaging Info

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

Packaging configurations for Oral Analgesic.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Meijer Oral Analgesic Liquid is formulated with a maximum strength of 20% benzocaine, providing fast relief from oral pain associated with toothaches, denture or gum irritations, and cold or canker sores. The product is packaged in a safety-sealed tube tip to ensure integrity and safety. Each tube contains a net weight of 0.45 ounces (13.3 grams).

Uses and Indications

This drug is indicated for the fast relief of oral pain associated with toothache, denture or gum irritations, and cold or canker sores.

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

Dosage and Administration

Adults and children aged 2 years and older are instructed to apply the product topically to the affected area using a cotton swab or a clean fingertip. The application may be performed up to four times daily or as directed by a dentist or physician.

For children under 12 years of age, supervision is recommended during the use of this product to ensure safe and effective application.

In the case of children under 2 years of age, it is advised to consult a dentist or doctor prior to use.

Contraindications

Use is contraindicated in patients who exceed the directed dosage or use the product for more than 7 days without the guidance of a dentist or doctor. Additionally, contact with the eyes should be avoided to prevent potential irritation or injury.

Warnings and Precautions

The use of this product necessitates careful consideration of several warnings and precautions to ensure patient safety and efficacy.

Allergy Alert This product is contraindicated in individuals with a known history of allergy to local anesthetics, including but not limited to procaine, butacaine, benzocaine, or other "caine" anesthetics. Healthcare professionals should assess the patient's allergy history thoroughly before recommending this product.

Flammability The product is flammable; therefore, it must be kept away from fire or flame. Patients should be advised to avoid smoking during application and until the product has completely dried to mitigate the risk of fire hazards.

General Precautions While using this product, it is imperative to avoid contact with the eyes. Patients should adhere strictly to the recommended dosage and duration of use, which should not exceed 7 days unless directed otherwise by a dentist or physician.

Monitoring and Follow-Up Patients should be instructed to discontinue use and consult a healthcare provider if symptoms of a sore mouth do not improve within 7 days, or if they experience persistent or worsening irritation, pain, or redness. Additionally, any development of swelling, rash, or fever warrants immediate medical consultation.

Emergency Situations In the event of an overdose, it is crucial to seek emergency medical assistance or contact a Poison Control Center without delay. Prompt action is essential to address potential complications associated with overdose.

Side Effects

Patients should be aware of the potential adverse reactions associated with the use of this product. Serious warnings include an allergy alert; individuals with a history of allergy to local anesthetics such as procaine, butacaine, benzocaine, or other "caine" anesthetics should not use this product. Additionally, the product is flammable, and patients are advised to keep it away from fire or flame and to avoid smoking during applications and until the product has dried.

Common adverse reactions may occur when using this product. Patients should avoid contact with the eyes and adhere to the recommended usage guidelines, which specify not to use the product for more than 7 days unless directed by a dentist or doctor.

Patients are advised to stop using the product and consult a healthcare professional if sore mouth symptoms do not improve within 7 days, or if irritation, pain, or redness persists or worsens. Furthermore, if swelling, rash, or fever develops, medical advice should be sought immediately.

In the event of an overdose, patients should seek medical help or contact a Poison Control Center without delay.

Drug Interactions

Patients with a known history of allergy to local anesthetics, including procaine, butacaine, benzocaine, or other "caine" anesthetics, should avoid the use of 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 Oral Analgesic (benzocaine). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Oral Analgesic.
Details

Pediatric Use

Pediatric patients under 12 years of age should be supervised during the use of this product to ensure safe application. For children under 2 years of age, it is recommended to consult a dentist or doctor prior to use.

For children aged 2 years and older, the product should be applied to the affected area using a cotton swab or a clean fingertip. The application may be performed up to four times daily or as directed by a healthcare professional.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

There are no specific statements regarding the use of Oral Analgesic Maximum Strength - benzocaine liquid during pregnancy. As such, there are no established safety concerns, dosage modifications, or special precautions for pregnant patients. Healthcare professionals should consider the lack of data when advising women of childbearing potential and weigh the potential benefits against any unknown risks to fetal outcomes. It is recommended that healthcare providers exercise caution and discuss the use of this product with pregnant patients, taking into account individual circumstances and the absence of specific pregnancy-related information in the prescribing information.

Lactation

There are no specific warnings or recommendations regarding the use of this product by lactating mothers. Additionally, there is no information available concerning the potential for excretion in breast milk or any effects on breastfed infants.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the prescribing information regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment and monitoring of these patients.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of 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 in these patients to ensure their safety during treatment.

Overdosage

In the event of an overdose, it is imperative to seek immediate medical assistance or contact a Poison Control Center without delay. Prompt intervention is crucial to mitigate potential adverse effects associated with the overdose.

Healthcare professionals should be aware that the specific symptoms of an overdose may vary depending on the substance involved. Therefore, a thorough assessment of the patient's condition is essential to determine the appropriate course of action.

Management of an overdose typically involves supportive care and symptomatic treatment. Continuous monitoring of the patient's vital signs and clinical status is recommended. In cases where the specific substance is known, targeted therapies may be employed as indicated.

It is essential for healthcare providers to remain vigilant and act swiftly in the management of overdose situations to ensure optimal patient outcomes.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children. In the event of an overdose, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be instructed to avoid contact with the eyes while using this product. They should not exceed the recommended dosage or use the product for more than 7 days unless directed by a dentist or doctor.

Additionally, healthcare providers should inform patients to discontinue use and consult a doctor if sore mouth symptoms do not improve within 7 days, or if they experience persistent or worsening irritation, pain, or redness. Patients should also be advised to seek medical attention if they develop swelling, a rash, or fever.

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 topically and may be used up to four times daily, or as directed by a dentist or doctor. 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 Oral Analgesic, 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 Oral Analgesic, 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

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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.