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Walgreens Cold Sore Treatment

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This product has been discontinued

Active ingredient
Benzocaine 5.00 mg/1 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2015
Label revision date
April 1, 2015
Active ingredient
Benzocaine 5.00 mg/1 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2015
Label revision date
April 1, 2015
Manufacturer
Walgreens
Registration number
part348
NDC root
0363-3191

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Drug Overview

Well at Walgreens Cold Sore Treatment is a medication specifically designed to help treat cold sores and fever blisters that appear on the face and lips. Cold sores are caused by the herpes simplex virus, and this treatment aims to alleviate the symptoms associated with these outbreaks.

By using this product, you can find relief from the discomfort of cold sores, helping to speed up the healing process and reduce the duration of the outbreak. It's a supportive option for managing the effects of this common viral condition.

Uses

If you're dealing with cold sores or fever blisters on your face and lips, this medication can help treat those uncomfortable outbreaks. Cold sores are caused by the herpes simplex virus, and they often appear as painful, fluid-filled blisters. Using this treatment can speed up healing and reduce the duration of your symptoms, helping you feel more comfortable and confident.

Dosage and Administration

When using this cream, you should apply it to the affected area no more than four times a day. If you are applying it for a child who is under 2 years old, it's important to consult a physician (doctor) first. To use the cream, gently rub it into the skin; it will go on clear, so it won’t leave a noticeable residue.

Before and after you apply the cream, make sure to wash your hands thoroughly. This helps prevent the spread of germs and ensures that the cream works effectively. Remember, this product is for your use only, so do not share it with anyone else.

What to Avoid

There are no specific contraindications, controlled substance classifications, or risks of abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular situations or conditions under which you should avoid using it. Always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

If you have a history of allergies to local anesthetics, such as procaine, butocaine, benzocaine, or any other “caine” anesthetics, it is important not to use this product. Allergic reactions can be serious, and avoiding these medications can help prevent potential complications. Always consult with your healthcare provider if you have concerns about allergies or side effects related to your treatment.

Warnings and Precautions

This product is for external use only, so please avoid using it on your eyes or over large areas of your body. If you have a history of allergies to local anesthetics like procaine, butocaine, or benzocaine, do not use this product. If you have deep or puncture wounds, animal bites, or serious burns, it's important to consult a physician before use.

While using this product, be careful to avoid contact with your eyes and follow the directions provided. If your condition worsens or does not improve after one week, stop using the product and contact your doctor. If you accidentally swallow it, seek medical help immediately or call the Poison Control Center at 1-800-222-1222.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs or symptoms of an overdose for this medication, general signs can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or have concerns about a possible overdose, seek medical help right away. It's always better to err on the side of caution when it comes to your health. Remember, if you are ever in doubt, contacting a healthcare professional is the best course of action.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the drug insert does not provide specific information about the use of this product during pregnancy. There are no warnings indicating that the product is unsafe for use while pregnant, nor are there any known risks to the fetus mentioned. Additionally, there are no dosage adjustments or special precautions outlined for pregnant individuals.

As always, it's best to consult with your healthcare provider before using any medication during pregnancy to ensure it is safe for you and your baby.

Lactation Use

If you are breastfeeding and considering using Walgreens Cold Sore Treatment, which contains benzocaine ointment, it's important to note that there is no specific information available about its effects on nursing mothers or lactation. This means that the potential impact on your breast milk or your nursing infant is not clearly understood.

As a precaution, you may want to consult with your healthcare provider before using this product while breastfeeding. They can help you weigh the benefits and risks based on your individual situation.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 2 years and older, you can apply it to the affected area up to four times a day. However, if your child is under 2 years old, you should consult a physician (doctor) before using it. This ensures that the treatment is safe and appropriate for their age. Always prioritize your child's health by seeking professional advice when needed.

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 for personalized advice. 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 may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

Drug Interactions

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

While there are no specific laboratory test interactions noted, it's always a good practice to inform your healthcare provider about all the medications and supplements you are using. This ensures that they can provide you with the safest and most effective care tailored to your needs.

Storage and Handling

To ensure the best use of your product, store it at room temperature, away from direct sunlight and moisture. It's important to keep it out of reach of children to prevent accidental use. Always wash your hands before and after applying the cream to maintain hygiene and safety. Remember, this product is for your personal use only, so do not share it with anyone else. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply this topical medication to the affected area no more than four 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. Always wash your hands before and after applying the cream to ensure cleanliness.

If the cream is accidentally swallowed, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222. Remember, do not share this product with anyone to avoid potential misuse.

FAQ

What is Well at Walgreens Cold Sore Treatment used for?

It is used for the treatment of cold sores and fever blisters on the face and lips.

How should I apply Well at Walgreens Cold Sore Treatment?

Apply to the affected area not more than 4 times daily for adults and children 2 years of age and older. For children under 2 years, consult a physician.

What should I do before and after applying the cream?

You should wash your hands before and after applying the cream.

Are there any allergy alerts for this product?

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

What should I do if I accidentally swallow the cream?

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Can I use this product if I am pregnant?

There is no specific information regarding use during pregnancy, and no contraindications are mentioned.

Is this product safe for nursing mothers?

No specific information regarding nursing mothers or lactation is provided.

How should I store Well at Walgreens Cold Sore Treatment?

Store at room temperature and keep out of reach of children.

Can I share this product with others?

No, do not share this product with anyone.

What should I do if my condition worsens?

Stop use and ask a doctor if the condition gets worse. Do not use longer than 1 week unless directed by a doctor.

Packaging Info

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

Packaging configurations for Walgreens Cold Sore Treatment.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Well at Walgreens Cold Sore Treatment is a topical formulation designed for the management of cold sores. The product is presented in a convenient dosage form suitable for application to affected areas. It is specifically formulated to alleviate symptoms associated with cold sores, providing targeted relief. The appearance of the treatment is consistent with standard topical applications, ensuring ease of use for patients.

Uses and Indications

This drug is indicated for the treatment of cold sores and fever blisters located on the face and lips.

Dosage and Administration

Adults and children aged 2 years and older are instructed to apply the cream to the affected area up to four times daily. For children under 2 years of age, it is recommended to consult a physician prior to use.

The cream should be gently rubbed into the skin and will apply clear. It is essential to wash hands thoroughly before and after application to prevent unintended exposure. Additionally, this product should not be shared with others to ensure safety and efficacy.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence. Additionally, there are no specific instructions indicating that the product should not be taken or used under any circumstances.

Warnings and Precautions

For external use only, this product carries specific warnings and precautions that must be adhered to in order to ensure safe usage.

Allergy Alert Individuals with a known history of allergy to local anesthetics, including procaine, butocaine, benzocaine, or other “caine” anesthetics, should not use this product.

Application Guidelines This product is not intended for use in the eyes or for application over large areas of the body. In instances of deep or puncture wounds, animal bites, or serious burns, it is imperative to consult a physician prior to use. Care should be taken to avoid contact with the eyes during application. The product should only be used as directed.

Monitoring and Duration of Use Users are advised to discontinue use and seek medical advice if the condition worsens. The product should not be used for longer than one week unless specifically directed by a healthcare professional.

Emergency Information In the event of accidental ingestion, immediate medical assistance should be sought, or contact should be made with a Poison Control Center at 1-800-222-1222.

Side Effects

Patients should be advised not to use this product if they have a history of allergy to local anesthetics, including but not limited to procaine, butocaine, benzocaine, or other “caine” anesthetics. The potential for serious allergic reactions necessitates careful consideration of the patient's medical history prior to administration.

Drug Interactions

Patients with a known history of allergy to local anesthetics, including procaine, butocaine, benzocaine, or other "caine" anesthetics, should avoid the use of this product due to the potential for severe allergic reactions.

No specific interactions with laboratory tests have been identified in the available data. Therefore, routine monitoring of laboratory tests is not indicated in relation to this product.

Packaging & NDC

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

Packaging configurations for Walgreens Cold Sore Treatment.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area up to four times daily. For children under 2 years of age, it is recommended to consult a physician prior to use.

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

Pregnant patients should be aware that no specific information regarding the use of this product during pregnancy is provided in the drug insert. There are no statements indicating whether the product is contraindicated in pregnancy or any associated risks to the fetus. Additionally, no dosage modifications or special precautions regarding use during pregnancy are mentioned. Healthcare professionals are encouraged to consider the absence of data when advising women of childbearing potential and to weigh the potential benefits against any unknown risks when prescribing this product to pregnant patients.

Lactation

There is no specific information available regarding the use of Walgreens Cold Sore Treatment (benzocaine ointment) in lactating mothers or its effects on breastfed infants. Healthcare professionals should consider the lack of data when advising lactating mothers on the use of this product.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

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 an overdose. Symptoms 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 the management of the overdose effectively.

Documentation of the incident, including the substance involved, the amount taken, and the time of ingestion, is crucial for appropriate 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 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 in the event of accidental ingestion, it is crucial to seek medical assistance immediately. Patients should be informed to contact a Poison Control Center at 1-800-222-1222 for guidance. Emphasizing the importance of prompt action in such situations can help ensure patient safety and appropriate care.

Storage and Handling

This product is supplied in a configuration that ensures optimal use and safety. It should be stored at room temperature, away from direct sunlight and moisture. To maintain safety, it is imperative to keep the product out of reach of children.

Prior to application, users are advised to wash their hands thoroughly to prevent contamination. After application, hands should be washed again to ensure hygiene. It is important to note that this product is intended for individual use and should not be shared with others.

Additional Clinical Information

The product is administered topically, with a recommended application frequency of up to four times daily for adults and children aged 2 years and older. For children under 2 years of age, consultation with a physician is advised prior to use.

Clinicians should counsel patients on the importance of seeking immediate medical assistance or contacting a Poison Control Center at 1-800-222-1222 if the product is swallowed. Patients are also advised not to share the product with others and to wash their hands before and after applying the cream to ensure proper hygiene.

Drug Information (PDF)

This file contains official product information for Walgreens Cold Sore Treatment, 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 Cold Sore Treatment, 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.