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Biofreeze Professional

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Active ingredient
Menthol, Unspecified Form 105 mg/1 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2016
Label revision date
December 27, 2024
Active ingredient
Menthol, Unspecified Form 105 mg/1 mL
Other brand names
Dosage form
Spray
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2016
Label revision date
December 27, 2024
Manufacturer
RB Health (US) LLC
Registration number
M017
NDC root
59316-120

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Drug Overview

BiOFREEZE® is a professional menthol pain-relieving spray designed to provide temporary relief from minor aches and pains in muscles and joints. It can be particularly helpful for conditions such as simple backache, arthritis, strains, bruises, and sprains. The spray works by delivering menthol, which creates a cooling sensation that helps alleviate discomfort.

With its convenient 360° spray design, you can easily apply it to the affected areas for quick relief. Whether you're dealing with everyday muscle soreness or recovering from an injury, BiOFREEZE® offers a supportive option to help you feel more comfortable.

Uses

You can use this medication to temporarily relieve minor aches and pains in your muscles and joints. It is effective for various conditions, including simple backaches, arthritis, strains, bruises, and sprains. If you're dealing with any of these issues, this medication may help ease your discomfort and improve your mobility.

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, if you are an adult or a child aged 12 years or older, you should spray it onto the affected area of your skin. You can do this up to 3 to 4 times a day, and there's no need to massage it into your skin. If the user is a child under 12 years old, it's important to consult a physician (doctor) before use to ensure safety and proper guidance.

After applying the spray, make sure to wash your hands with cool water to avoid any unwanted contact with your eyes or other sensitive areas. Following these steps will help you use the medication effectively and safely.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should not apply it to wounds or damaged skin, as this can lead to further complications. Additionally, avoid using it on irritated skin or if you notice excessive irritation developing. Be cautious not to bandage the area tightly, and refrain from using it in conjunction with heating pads or devices, as this can increase the risk of adverse effects. Following these guidelines will help ensure your safety while using the product.

Side Effects

When using this product, it's important to be aware of potential side effects. You should avoid contact with your eyes and mucous membranes, and do not apply it to wounds, damaged, or irritated skin. If you experience pain, swelling, or blistering of the skin, or if your condition worsens or does not improve after 7 days, stop using the product and consult a doctor. Additionally, if you have arthritic pain that lasts more than 10 days or notice any redness, seek medical advice.

If you are pregnant or breastfeeding, please consult a healthcare professional before using this product. Keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately. Remember, this product is for external use only and is flammable, so keep it away from heat and open flames.

Warnings and Precautions

This product is for external use only, so please avoid applying it to your eyes or ingesting it. It is flammable, so keep it away from heat sources and open flames. The container is under pressure, which means you should not puncture or incinerate it, and be sure to store it at temperatures below 120°F.

If you notice any pain, swelling, or blistering of the skin, or if your condition worsens or does not improve after 7 days, stop using the product and consult your doctor. Additionally, if you have arthritic pain that lasts more than 10 days or if you see redness, it's important to seek medical advice. Always keep this product out of reach of children, and if it is swallowed, get medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose has occurred.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

When using this medication, it's important to follow specific guidelines for children. For adults and children aged 12 and older, you can apply the spray to the affected area up to 3 to 4 times a day, and there's no need to massage it in. However, if your child is under 12 years old, you should consult a physician (doctor) before using this product to ensure it's safe and appropriate for them. 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 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 is safe and effective for your specific health needs. They can help determine the best approach for managing your condition while considering your kidney health.

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 differently due to your liver health.

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

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, always ensure that your healthcare provider is aware of all the medications you are using, as this helps them provide the best care tailored to your needs.

By discussing your full medical history and any other treatments, you can help prevent potential issues and ensure your safety.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 20-25°C (68-77°F). It's important to keep it away from direct sunlight, as exposure can affect its quality.

When handling the product, always do so with clean hands and in a clean environment to maintain its integrity. If you have any specific disposal instructions, please follow them carefully to ensure safety.

Additional Information

You should apply this medication topically, spraying it onto the affected area no more than 3 to 4 times a day. For children under 12 years old, it's important to consult a physician before use. If you are pregnant or breastfeeding, be sure to ask a healthcare professional for advice before using this product.

Keep the medication out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately.

FAQ

What is BiOFREEZE®?

BiOFREEZE® is a professional menthol-pain relieving spray that temporarily relieves minor aches and pains of muscles and joints.

What conditions can BiOFREEZE® help relieve?

BiOFREEZE® can help relieve simple backache, arthritis, strains, bruises, and sprains.

How should I use BiOFREEZE®?

For adults and children 12 years and older, spray on the affected area 3 to 4 times daily. For children under 12, consult a physician.

Are there any contraindications for using BiOFREEZE®?

No specific contraindications are mentioned for BiOFREEZE®.

What should I avoid while using BiOFREEZE®?

Avoid contact with eyes, applying to wounds or damaged skin, and using with heating pads or tight bandages.

What should I do if I experience side effects?

Stop use and consult a doctor if you experience pain, swelling, blistering, or if symptoms persist for more than 7 days.

Is BiOFREEZE® safe to use during pregnancy or breastfeeding?

If you are pregnant or breastfeeding, consult a health professional before using BiOFREEZE®.

How should I store BiOFREEZE®?

Store BiOFREEZE® at 20-25°C (68-77°F) in a cool, dry place away from direct sunlight.

What should I do if BiOFREEZE® is swallowed?

Keep BiOFREEZE® out of reach of children. If swallowed, seek medical help or contact a Poison Control Center immediately.

Packaging Info

Below are the non-prescription pack sizes of Biofreeze Professional (menthol, unspecified form). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Biofreeze Professional.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

BiOFREEZE® PROFESSIONAL is a menthol pain-relieving spray formulated for topical application. Each 4 fluid ounce (118 mL) container features a 360° spray mechanism, allowing for versatile application angles. The product is identified by National Drug Code (NDC) 59316-120-20. For initial use, it is necessary to press down firmly to activate the sprayer.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles and joints. Specifically, it is effective for conditions such as simple backache, arthritis, strains, bruises, and sprains.

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

Dosage and Administration

For adults and children aged 12 years and older, the recommended dosage is to spray the product onto the affected area no more than 3 to 4 times daily. It is not necessary to massage the area after application.

For children under 12 years of age, it is advised to consult a physician prior to use.

After application, it is important to wash hands thoroughly with cool water to prevent any unintended contact with sensitive areas.

Contraindications

The product is contraindicated in the following situations:

Application to wounds or damaged skin is prohibited due to the potential for adverse effects. Additionally, the product should not be applied to irritated skin or in cases where excessive irritation develops, as this may exacerbate the condition. Furthermore, tight bandaging or the use of heating pads or devices in conjunction with the product is contraindicated, as this may lead to increased risk of irritation or other complications.

Warnings and Precautions

For external use only. This product is flammable; therefore, it must be kept away from excessive heat or open flame to prevent fire hazards. The contents are under pressure; puncturing or incinerating the container is strictly prohibited to avoid potential injury.

Storage conditions are critical; do not store the product at temperatures exceeding 120°F to maintain its integrity and safety.

Healthcare professionals should advise patients to discontinue use and seek medical attention if any of the following occur: pain, swelling, or blistering of the skin; worsening of the condition; symptoms that persist for more than 7 days; or if symptoms resolve and then recur within a few days. Additionally, if arthritic pain continues for more than 10 days or if redness is observed, medical consultation is recommended.

It is essential to keep this product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is advised.

Side Effects

Patients using this product should be aware of several important warnings and precautions. The product is intended for external use only and is flammable; therefore, it should be kept away from excessive heat or open flames. Additionally, the contents are under pressure, and users should not puncture or incinerate the container. It is crucial to store the product at temperatures not exceeding 120°F.

When using this product, patients should avoid contact with the eyes and mucous membranes. It should not be applied to wounds, damaged skin, or irritated skin, especially if excessive irritation develops. Users are advised against tightly bandaging the area or using the product in conjunction with heating pads or devices.

Patients are instructed to stop use and consult a healthcare professional if they experience pain, swelling, or blistering of the skin. If the condition worsens, or if symptoms persist for more than 7 days or recur within a few days after improvement, medical advice should be sought. Furthermore, if arthritic pain persists for more than 10 days or if redness is present, patients should also seek medical attention.

Additional considerations include consulting a healthcare professional if pregnant or breastfeeding before using the product. It is essential to keep the product out of reach of children; in the event of ingestion, immediate medical assistance or contact with a Poison Control Center is recommended.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Biofreeze Professional (menthol, unspecified form). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Biofreeze Professional.
Details

Pediatric Use

Pediatric patients aged 12 years and older may use the product by spraying it onto the affected area no more than 3 to 4 times daily; massage is not necessary. For children under 12 years of age, consultation with a physician is advised 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 and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully considered in these populations to ensure the safety of both the mother and the fetus or infant.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data on the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating individuals.

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 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 prescribing information.

Overdosage

In the event of an overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. It is imperative that healthcare providers remain vigilant and prepared to address any complications that may arise from an overdosage scenario.

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 this product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, patients should seek medical help or contact a Poison Control Center immediately.

Patients should be instructed to discontinue use and consult a doctor if they experience any pain, swelling, or blistering of the skin. Additionally, they should be informed to stop using the product and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. For those experiencing arthritic pain, it is important to advise them to stop use and consult a doctor if the pain persists for more than 10 days or if redness is present.

When using this product, patients must be reminded to follow the directions carefully. They should avoid contact with the eyes and mucous membranes, and should not apply the product to wounds, damaged skin, or irritated skin. If excessive irritation develops, patients should discontinue use and consult a healthcare professional. Furthermore, patients should be cautioned against tightly bandaging the area or using the product in conjunction with a heating pad or device.

Storage and Handling

The product is supplied in packaging that ensures its integrity during storage. It should be stored at a temperature range of 20-25°C (68-77°F) and kept in a cool, dry place, away from direct sunlight. Proper storage conditions are essential to maintain the product's efficacy and safety.

Additional Clinical Information

The product is administered topically, with a recommended frequency of application for adults and children aged 12 years and older being 3 to 4 times daily, without the need for massage. For children under 12 years of age, consultation with a physician is advised prior to use.

Clinicians should counsel patients to seek advice from a health professional if they are pregnant or breastfeeding. Additionally, it is important to keep the product out of reach of children, and in the event of ingestion, medical assistance or contact with a Poison Control Center should be sought immediately.

Drug Information (PDF)

This file contains official product information for Biofreeze Professional, 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 Biofreeze Professional, 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.