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Beerx Cold Sore Treatment

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Active ingredient
Glycerin 0.2 g/1 g
Other brand names
Drug class
Non-Standardized Chemical Allergen
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2023
Label revision date
January 21, 2025
Active ingredient
Glycerin 0.2 g/1 g
Other brand names
Drug class
Non-Standardized Chemical Allergen
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2023
Label revision date
January 21, 2025
Manufacturer
Taro Pharmaceuticals U. S. A. , Inc.
Registration number
M017
NDC root
51672-5309

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Drug Overview

beeRX™ is an all-natural gel treatment specifically designed to relieve the symptoms of cold sores and fever blisters. It contains 20% plant-based glycerin and is made from 100% natural ingredients, making it a gentle option for soothing discomfort. This gel works by softening cold sores, reducing dryness, and promoting healing while providing a protective barrier to the affected area.

Clinically shown to alleviate symptoms, beeRX™ helps to soften crusts (scabs) associated with cold sores and supports the natural healing process. By moisturizing and soothing the skin, it aims to make you feel more comfortable during an outbreak.

Uses

If you're dealing with cold sores or fever blisters, this treatment can help you find relief. It works by softening and moisturizing the affected areas, which can ease dryness and discomfort. The gel is made from all-natural ingredients and has been clinically shown to alleviate symptoms associated with cold sores.

In addition to providing relief, this treatment also helps to soften any crusts (scabs) that may form, promoting natural healing. It creates a protective barrier over the cold sores, allowing them to heal more effectively while soothing the skin. With this gel, you can expect a more comfortable experience as you recover from cold sores and fever blisters.

Dosage and Administration

If you have a child under 1 year old, it's important to consult a doctor before using this medication. For older children and adults, you should apply the medication directly to the affected area, such as a cold sore or fever blister, at least five times a day. You can apply it more often if needed.

Once applied, the medication is safe to leave on the skin for extended periods. Be sure to discard the product once the cold sore or fever blister has completely healed to ensure proper hygiene and effectiveness.

What to Avoid

It's important to be cautious when using this medication. You should not use it on deep puncture wounds, animal bites, or serious burns, as these conditions require different medical attention.

Additionally, be aware that this medication is classified as a controlled substance, which means it has the potential for abuse or misuse. This can lead to dependence (a condition where your body becomes reliant on a substance). Always follow your healthcare provider's instructions and avoid using this medication inappropriately.

Side Effects

It's important to use this product only on the outside of your body. If you notice that your condition is getting worse, or if your symptoms last longer than seven days, you should stop using the product and consult your healthcare professional. Additionally, if your symptoms improve and then return within a few days, it's also a good idea to seek medical advice.

Warnings and Precautions

This product is for external use only, so please avoid applying it to any areas that are deep puncture wounds, animal bites, or serious burns. It's important to keep this product out of the reach of children to ensure their safety.

If your condition worsens, or if your symptoms last more than 7 days or improve and then return within a few days, stop using the product and contact your healthcare professional for further advice. While there are no specific emergency instructions provided, always seek immediate medical help if you experience any severe reactions or concerns.

Overdose

If you suspect an overdose of this medication, it's important to stay calm and take immediate action. While the drug insert does not provide specific information about overdose, you should be aware of general signs that may indicate an overdose, such as unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms, seek medical help right away. It's always better to err on the side of caution when it comes to your health. If you are ever in doubt, contacting a healthcare professional or poison control can provide you with the guidance you need.

Pregnancy Use

The safety of this product during pregnancy has not been evaluated, meaning there is limited information on its effects. However, there are no specific contraindications (reasons not to use it) mentioned for pregnant individuals, and the insert does not highlight any particular safety concerns or risks to the fetus. Additionally, no dosage adjustments are recommended for those who are pregnant, and no special precautions are noted.

As always, it's important to discuss any medications or products you are considering with your healthcare provider, especially if you are pregnant or planning to become pregnant. They can provide personalized advice based on your health and circumstances.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the effects of this medication on nursing mothers or lactation (the process of producing breast milk). Since there are no guidelines or data provided, it’s advisable to consult with your healthcare provider to discuss any potential risks or concerns related to your situation. They can help you make informed decisions that prioritize both your health and your baby's well-being.

Pediatric Use

If your child is under 1 year old, it's important to consult a doctor before using this product. For older children, you can apply it to the affected area at least five times a day, or as often as needed. It's safe to leave the product on the skin for extended periods, but remember not to share it with anyone else. Once the cold sore or fever blister has healed, be sure to discard the 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 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 your medication dosage may need to be adjusted. Regular monitoring of your kidney function is essential, and your healthcare provider will likely assess your creatinine clearance (a test that measures how well your kidneys are filtering waste) to determine the right dosing for you.

If your renal function is decreased, you may require a lower dose of your medication to ensure safety and effectiveness. Always discuss any concerns with your healthcare provider, as they will consider these factors to provide the best care for your situation.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help monitor your liver function and determine the best approach for your treatment.

Make sure to keep your doctor informed about your liver health, as they may need to conduct regular liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and tests during your appointments.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool, dry place at a temperature between 20 to 25°C (68-77°F). It's important to check the packaging before use; do not use the product if the outer seals are broken or missing, as this could compromise its safety.

Make sure to keep the original carton, as it contains important warnings and information that you may need later. Following these guidelines will help you handle the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is beeRX™?

beeRX™ is an all-natural cold sore gel treatment that is clinically shown to relieve cold sore symptoms.

How does beeRX™ work?

It relieves dryness, softens cold sores and fever blisters, reduces discomfort, and promotes natural healing.

What are the key ingredients in beeRX™?

beeRX™ contains 20% plant-based glycerin and 100% natural ingredients.

How should I use beeRX™?

Apply it to the affected area at least 5 times a day, and as often as required. It is safe to leave on the skin for long periods.

Are there any warnings for using beeRX™?

Yes, it is for external use only. Do not use on deep puncture wounds, animal bites, or serious burns.

What should I do if my condition worsens?

Stop using beeRX™ and see your healthcare professional if your condition worsens or if symptoms last more than 7 days.

Is beeRX™ safe for children?

Consult a doctor before using beeRX™ on children under 1 year.

Can I use beeRX™ during pregnancy?

The product has not been evaluated for safety during pregnancy, and no specific contraindications are mentioned.

How should I store beeRX™?

Store beeRX™ at 20 to 25°C (68-77°F) and do not use if the outer seals are broken or missing.

Packaging Info

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

Packaging configurations for Beerx Cold Sore Treatment.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

beeRX™ is a non-toxic, cold sore treatment formulated with 20% plant-based glycerin and New Zealand kanuka honey. This 100% natural gel, weighing 0.35 oz (10 g), is clinically shown to relieve cold sore symptoms, reduce discomfort, and promote healing. It provides a protective barrier to cold sores while soothing and moisturizing the affected area. The product is free from colorants and fragrances, and it has not been tested on animals. Manufactured in Australia, beeRX™ is naturally sourced and should be stored at a temperature of 20-25°C (68-77°F).

Uses and Indications

This drug is indicated for the relief of dryness and softening of cold sores and fever blisters. It is formulated as an all-natural gel treatment that has been clinically shown to alleviate symptoms associated with cold sores. The product softens crusts (scabs) related to cold sores and fever blisters, reduces discomfort, and promotes natural healing.

Additionally, this drug provides a protective barrier to cold sores, while soothing and moisturizing the affected area to enhance the healing process. There are no known teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

For children under 1 year of age, it is recommended to consult a healthcare professional prior to use. The product should be applied to the affected area(s) at least five times a day, or as often as necessary, to achieve optimal results. It is safe to leave the product on the skin for extended periods. Once the cold sore or fever blister has healed, the product should be discarded.

Contraindications

Use is contraindicated in patients with deep puncture wounds, animal bites, or serious burns. These conditions may increase the risk of complications or adverse effects associated with the product.

Warnings and Precautions

External use only is strictly advised for this product. It is imperative that the product is kept out of reach of children to prevent accidental ingestion or misuse.

The product should not be applied to deep puncture wounds, animal bites, or serious burns, as these conditions may require different medical interventions and could lead to complications if treated improperly.

Healthcare professionals should instruct patients to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Monitoring for these signs is essential to ensure appropriate management and to prevent potential adverse effects.

Side Effects

Patients should be aware that the product is intended for external use only. In the event that the condition worsens, or if symptoms persist for more than 7 days or resolve only to recur within a few days, it is advised to discontinue use and consult a healthcare professional. These precautions are essential to ensure the safety and well-being of individuals using the product.

Drug Interactions

There are no reported drug interactions associated with the use of this medication. Additionally, no interactions with laboratory tests have been identified. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Beerx Cold Sore Treatment.
Details

Pediatric Use

Pediatric patients under 1 year of age should consult a healthcare professional before using this product. For children aged 1 year and older, the product should be applied to the affected area(s) at least 5 times a day, or as often as required. It is safe to leave the product on the skin for extended periods. Healthcare professionals should advise against sharing this product with others. Once the cold sore or fever blister has healed, the product should be discarded.

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

The product has not been evaluated for safety during pregnancy. There are no specific contraindications for use during this period, and the insert does not provide any specific safety concerns or risks to the fetus associated with the use of this product during pregnancy. Additionally, no dosage modifications for pregnant individuals are mentioned, and no special precautions regarding use during pregnancy are provided. Healthcare professionals should consider the lack of data when prescribing this product to pregnant patients and weigh the potential benefits against any unknown risks.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established.

Renal Impairment

Patients with renal impairment may necessitate dosage adjustments based on their level of kidney function. It is essential for healthcare professionals to regularly monitor the renal function of these patients to ensure safe and effective treatment.

Creatinine clearance should be assessed to determine the appropriate dosing regimen, as reduced doses may be required for patients with decreased renal function. Additionally, safety considerations must be taken into account for patients with kidney problems to mitigate potential risks associated with medication use.

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 in the available sections of the drug insert, healthcare professionals are advised to exercise caution and consider general principles of management for potential overdosage scenarios.

Recommended Actions

In the event of suspected overdosage, it is essential for healthcare providers to assess the patient's clinical status promptly. Monitoring vital signs and conducting a thorough evaluation of symptoms is crucial.

Potential Symptoms

While specific symptoms related to overdosage are not detailed, healthcare professionals should remain vigilant for any unusual or severe reactions that may arise, as these could indicate an adverse response to the medication.

Management Procedures

Management of overdosage should be tailored to the individual patient and may include supportive care and symptomatic treatment. In cases where the overdosage is confirmed or suspected, contacting a poison control center or seeking expert consultation is recommended to ensure appropriate management strategies are implemented.

Healthcare professionals are encouraged to report any cases of overdosage to the relevant authorities to contribute to the ongoing assessment of the drug's safety profile.

Nonclinical Toxicology

No teratogenic or non-teratogenic effects have been reported in the available nonclinical studies. Additionally, there is no information regarding animal pharmacology and toxicology. The absence of data limits the assessment of potential risks associated with the compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion or misuse.

Patients should be informed not to use the medication on deep puncture wounds, animal bites, or serious burns, as these conditions may require different treatment approaches.

Additionally, healthcare providers should instruct patients to discontinue use and seek medical attention if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. This guidance is essential to ensure appropriate management of their condition and to prevent potential complications.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers, which should be referenced for identification. It is essential to store the product at a controlled temperature range of 20 to 25°C (68 to 77°F) to maintain its integrity and efficacy.

Healthcare professionals are advised to inspect the outer seals of the packaging prior to use; the product should not be utilized if the seals are broken or missing. Additionally, it is recommended to retain the carton for access to full warnings and information regarding the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Beerx 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 Beerx 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.

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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.