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Walgreens Pain Relief

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Active ingredient
Benzocaine 200 mg/1 g
Other brand names
Drug class
Standardized Chemical Allergen
Dosage form
Gel
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2013
Label revision date
November 20, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Benzocaine 200 mg/1 g
Other brand names
Drug class
Standardized Chemical Allergen
Dosage form
Gel
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 2013
Label revision date
November 20, 2024
Manufacturer
Walgreens Company
Registration number
M017
NDC root
0363-5061
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

Walgreens Oral Pain Relief is a maximum strength topical gel that contains 20% benzocaine, a medication that helps numb pain. It is designed to provide fast relief from toothache pain and is also effective for temporary relief of occasional minor irritation and soreness in the mouth.

This product is particularly useful if you're experiencing discomfort in your mouth and need quick relief. With its easy-to-use gel formulation, it can help soothe your symptoms and make you feel more comfortable.

Uses

You can use this medication for the temporary relief of occasional minor irritation, pain, and soreness in your mouth. It’s designed to help soothe discomfort, making it easier for you to eat and speak comfortably.

Rest assured, there are no known teratogenic effects (which means it doesn’t cause birth defects) associated with this medication, so it is considered safe in that regard.

Dosage and Administration

When using the Oral Pain Relief Gel, start by ensuring the tube is intact; do not use it if it has been cut before opening. To prepare the gel, cut open the tip of the tube at the score mark. Then, using your fingertip or a cotton applicator, apply a small amount—about the size of a pea—to the area that is causing discomfort.

You can apply the gel to the affected area up to four times a day, or as your dentist or physician advises. This product is suitable for adults and children aged 2 years and older. If you are using it for a child under 12, make sure they are supervised during application. For children under 2 years of age, it’s important to consult a doctor before use.

What to Avoid

It's important to use this medication responsibly. You should not take more than the directed amount, and avoid using it for longer than 7 days unless your dentist or doctor specifically advises you to do so. Following these guidelines helps ensure your safety and the effectiveness of the treatment. If you have any questions or concerns, don't hesitate to reach out to your healthcare provider for guidance.

Side Effects

If you have a history of allergies to local anesthetics like procaine, butacaine, or benzocaine, you should not use this product. It's important to follow the recommended dosage and not use it for more than 7 days unless directed by a dentist or doctor.

You should stop using the product and consult a doctor if you experience any swelling, rash, or fever. Additionally, if you notice irritation, pain, or redness that persists or worsens, seek medical advice.

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, benzocaine, or other "caine" anesthetics, do not use this product. Always follow the directions carefully and avoid using it for more than 7 days unless your dentist or doctor advises otherwise.

If you experience any swelling, rash, or fever, stop using the product and call your doctor. Additionally, if you notice irritation, pain, or redness that persists or worsens, it's important to seek medical advice. In the event 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.

Don’t wait to see if symptoms improve; prompt action can be vital. Always prioritize your health and safety by reaching out for professional assistance in these situations.

Pregnancy Use

When it comes to using benzocaine during pregnancy, there is currently no specific information available about its safety, recommended dosages, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before using benzocaine. They can help you weigh the potential risks and benefits based on your individual situation. Always prioritize your health and the health of your baby by seeking professional advice.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your doctor before using this product. There is a possibility that it may be excreted in breast milk, which means it could potentially affect your baby. Since the effects on nursing infants have not been thoroughly studied, it's best to approach this with caution. Always prioritize your health and your baby's well-being by discussing any concerns with your healthcare provider.

Pediatric Use

When using this product for children aged 2 years and older, you can apply it directly to the affected area. However, if your child is under 12 years old, it's important to supervise them during use to ensure safety. For children younger than 2 years, you should consult a doctor before using the product to get appropriate guidance. Always prioritize your child's safety and well-being when considering any medication.

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, it’s important to consult with a healthcare provider before starting the medication. 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 drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if your kidneys are not functioning properly.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your kidney health. They can help monitor your condition and make any necessary adjustments to 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 should be used if you have hepatic impairment (issues with liver function).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

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 your provider make the best decisions for your health.

Storage and Handling

To ensure the best performance of your product, store it at a controlled room temperature between 59°F and 86°F (15°C and 30°C). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, make sure to do so in a clean environment to avoid contamination. Always follow any specific instructions provided for use and disposal to ensure safety and compliance.

Additional Information

You can take this medication orally and apply it to the affected area up to four times a day, or as directed by your dentist or physician. Make sure to follow their instructions for the best results. If you have any questions or concerns about how to use this medication, don't hesitate to reach out to your healthcare provider for guidance.

FAQ

What is Walgreens Oral Pain Relief?

Walgreens Oral Pain Relief is a maximum strength gel containing 20% benzocaine, designed for fast relief of toothache pain.

What are the indications for using this product?

It provides temporary relief of occasional minor irritation, pain, and sore mouth.

How should I use Walgreens Oral Pain Relief?

Apply a small pea-size amount to the affected area using your fingertip or a cotton applicator, up to four times daily or as directed by a dentist or physician.

Who can use this product?

Adults and children 2 years of age and older can use it, but children under 12 should be supervised, and those under 2 should consult a doctor.

Are there any contraindications for this product?

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

What should I do if I experience side effects?

Stop use and ask a doctor if swelling, rash, or fever develops, or if irritation, pain, or redness persists or worsens.

Can I use this product during pregnancy?

The insert does not provide specific information regarding the use of benzocaine during pregnancy, so consult your doctor.

Is it safe to use while nursing?

Nursing mothers should consult a doctor before using this product, as there is potential for excretion in breast milk.

What should I do in case of overdose?

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

How should I store Walgreens Oral Pain Relief?

Store at a controlled room temperature between 59°-86°F (15°-30°C).

Packaging Info

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

Packaging configurations for Walgreens Pain Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

20% Benzocaine Topical Gel is a topical anesthetic formulation containing 20% benzocaine as the active ingredient. The product is packaged in a net weight of 0.33 ounces (9.35 grams). It is manufactured in the United States.

Uses and Indications

This drug is indicated for the temporary relief of occasional minor irritation, pain, and soreness in the mouth.

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

Dosage and Administration

The tube should not be used if it is cut prior to opening. To prepare the product for use, the tip of the tube must be cut open at the designated score mark. A small pea-sized amount of Oral Pain Relief Gel should be applied to the affected area using either a fingertip or a cotton applicator.

For adults and children aged 2 years and older, the gel may be applied to the affected area up to four times daily, or as directed by a dentist or physician. It is important that children under 12 years of age are supervised during the application of this product. For children under 2 years of age, consultation with a doctor is recommended prior to use.

Contraindications

There are no specific contraindications identified for this product. However, it is advised that the product should not be used in excess of the directed dosage. Additionally, use should not exceed 7 days unless directed by a dentist or physician.

Warnings and Precautions

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

It is imperative that the product is used strictly as directed. Prolonged use beyond 7 days is not recommended unless specifically advised by a dentist or physician. Adhering to these guidelines is essential to minimize the risk of adverse effects.

Healthcare professionals should instruct patients to discontinue use and seek medical attention if they experience any of the following symptoms: swelling, rash, or fever. Additionally, if irritation, pain, or redness persists or worsens, patients should be advised to contact their healthcare provider promptly.

In the event of an overdose, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay to ensure appropriate management of the situation.

Side Effects

Patients should be aware of the potential adverse reactions associated with this product. A significant warning includes 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.

It is crucial for patients to adhere to the recommended usage guidelines. The product should not be used more than directed or for a duration exceeding 7 days unless specifically instructed by a dentist or doctor.

Patients are advised to discontinue use and consult a healthcare professional if they experience any of the following symptoms: swelling, rash, or fever. Additionally, if irritation, pain, or redness persists or worsens, medical advice should be sought promptly.

Drug Interactions

The use of 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.

No specific drug or laboratory test interactions have been identified in the available data. Therefore, no additional monitoring or dosage adjustments are recommended based on drug interactions.

Packaging & NDC

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

Packaging configurations for Walgreens Pain Relief.
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, supervision is recommended during the use of this product to ensure safety and proper application. In infants and children under 2 years of age, it is advised to consult a 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population, given the lack of targeted data.

Pregnancy

The safety of benzocaine use during pregnancy has not been established, as the prescribing information does not provide specific data regarding its use in this population. Consequently, healthcare professionals should exercise caution when considering benzocaine for pregnant patients. There are no available studies detailing potential risks or fetal outcomes associated with benzocaine exposure during pregnancy. Given the lack of information, it is advisable to weigh the potential benefits against any unknown risks before prescribing benzocaine to women of childbearing potential.

Lactation

Nursing mothers should consult a doctor before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are not well studied; therefore, caution is advised.

Renal Impairment

There is no specific information regarding renal impairment, dosage adjustments, special monitoring, or safety considerations for patients with reduced kidney function provided in the drug insert. Healthcare professionals should exercise caution when prescribing this medication to patients with renal impairment, as the lack of data may necessitate individualized assessment and monitoring based on the patient's overall clinical status.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this medication. Consequently, there are no 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 prescribing information.

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 substance is known, specific antidotes or treatments may be indicated, and healthcare providers should refer to established guidelines for the management of the particular overdose scenario.

It is vital for healthcare professionals to remain vigilant and act swiftly in the event of an overdose to ensure the best possible outcomes for affected individuals.

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 to keep the medication out of reach of children to prevent accidental ingestion. In the event of an overdose, patients should be instructed to seek medical help or contact a Poison Control Center immediately.

Patients must be cautioned not to exceed the recommended dosage and to refrain from using the medication for more than 7 days unless directed by a dentist or doctor. It is important for patients to be aware of potential adverse reactions; they should stop using the medication and consult a doctor if they experience swelling, rash, or fever. Additionally, patients should be informed to discontinue use and seek medical advice if irritation, pain, or redness persists or worsens.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It should be stored at a controlled room temperature ranging from 59°F to 86°F (15°C to 30°C). Proper storage conditions are essential to maintain the integrity of the product.

Additional Clinical Information

The medication is administered orally and should be applied to the affected area up to four times daily, or as directed by a dentist or physician. 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 Walgreens Pain Relief, 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 Walgreens Pain Relief, 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.