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Bio-Scriptives Extreme Pr

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This product has been discontinued

Active ingredient
Menthol 5.11 g/113 g
Other brand names
Dosage form
Lotion
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2011
Label revision date
July 22, 2011
Active ingredient
Menthol 5.11 g/113 g
Other brand names
Dosage form
Lotion
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2011
Label revision date
July 22, 2011
Manufacturer
BioChemics, Inc.
Registration number
part348
NDC root
60608-015

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Drug Overview

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is particularly helpful for discomfort associated with conditions like arthritis, sprains, strains, and back pain. This means that if you're experiencing these types of pain, this drug may provide you with some much-needed relief.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is particularly effective for discomfort associated with conditions like arthritis, sprains, strains, and back pain. If you're experiencing any of these issues, this medication may help alleviate your symptoms and improve your comfort.

Dosage and Administration

Before you start using Extreme PR™, make sure the safety seal is intact; do not use it if the seal is broken. To ensure the product works effectively, shake the bottle well before each application.

You can apply Extreme PR™ to the area that needs treatment, and it’s recommended to do this up to four times a day. Gently massage the product into the skin for the best results.

What to Avoid

It's important to be aware of certain guidelines when using this medication. While there are no specific contraindications or concerns about abuse, misuse, or dependence, you should stop using the medication and consult your doctor if your condition worsens or lasts longer than 7 days. This ensures that you receive the appropriate care and support for your health needs. Always prioritize your well-being and communicate openly with your healthcare provider.

Side Effects

It's important to be aware of some precautions when using this product. You should avoid contact with your eyes and refrain from using it on wounds or damaged skin, as it is intended for external use only.

If your condition worsens or does not improve after 7 days of use, please stop using the product and consult your doctor for further advice.

Warnings and Precautions

It’s important to use this product safely. Avoid getting it in your eyes, and do not apply it to wounds or damaged skin. Remember, this product is for external use only.

If your condition worsens or does not improve after 7 days, stop using the product and contact your doctor for further advice. Always prioritize your health and seek professional guidance when needed.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there are no specific details provided about the signs of an overdose, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your safety and health.

Pregnancy Use

There is currently no specific information available about the use of Bio-Scriptives Extreme PR - menthol lotion during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product to ensure it is safe for you and your baby. Always prioritize open communication with your doctor regarding any medications or topical treatments you may consider during this time.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding nursing mothers in the information provided. Additionally, there are no particular considerations or precautions mentioned for lactation. This suggests that the use of the medication may not pose significant risks to you or your nursing infant. However, it's always a good idea to consult with your healthcare provider about any medications you are taking while breastfeeding to ensure the best care for you and your baby.

Pediatric Use

It's important to keep this medication out of the reach of children. This precaution helps prevent accidental ingestion, which can be dangerous. Always store it in a safe place where children cannot access it, ensuring their safety at home. If you have any concerns or questions about the medication, don't hesitate to reach out to your healthcare provider for guidance.

Geriatric Use

While there is no specific information about how this medication should be used by older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions that may be present.

Remember, even if there are no specific dosage adjustments or safety concerns mentioned, your healthcare provider may still recommend monitoring for any potential side effects or interactions with other medications you may be taking. Always prioritize open communication with your healthcare team to ensure the best care.

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 information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you or how it should be managed in the context of liver impairment.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific health needs. They can help you understand how to manage your condition while considering any medications you may be taking.

Drug Interactions

It's great to know that there are no reported interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective.

Always keep your healthcare provider informed about any changes in your health or new medications you may start. Open communication helps prevent any potential issues and supports your overall well-being.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Always make sure the container is tightly closed when not in use to maintain its integrity. Once opened, please remember to discard the product to ensure safety and effectiveness. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply and massage Extreme PR™ onto the treatment area up to four times a day for optimal results. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling information.

FAQ

What is the primary use of this drug?

This drug is used for temporary relief of minor aches and pains of muscles and joints associated with arthritis, sprains, strains, and back pain.

How should I apply this drug?

You should apply and massage Extreme PR™ onto the treatment area up to 4 times daily.

Are there any contraindications for this drug?

No contraindications are listed for this drug.

What should I do if my condition worsens?

You should stop use and ask your doctor if your condition worsens or lasts more than 7 days.

What precautions should I take while using this drug?

Avoid contact with eyes, do not use on wounds or damaged skin, and remember that this product is for external use only.

How should I store this drug?

Store at room temperature, protect from light, do not freeze, and keep the container tightly closed. Discard after opening.

Is this drug safe to use during pregnancy or while nursing?

No specific information regarding safety during pregnancy or nursing is provided in the drug insert.

What should I do if the safety seal is broken?

Do not use the drug if the safety seal is broken.

What are the potential side effects of this drug?

No specific side effects are mentioned in the provided text.

Is there any information about drug interactions?

No drug interactions are mentioned in the provided text.

Packaging Info

Below are the non-prescription pack sizes of Bio-Scriptives Extreme Pr (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bio-Scriptives Extreme Pr.
Details

Drug Information (PDF)

This file contains official product information for Bio-Scriptives Extreme Pr, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of muscles and joints associated with arthritis, sprains, strains, and back pain.

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

Dosage and Administration

Healthcare professionals should ensure that the safety seal is intact before use. Prior to application, the product must be shaken well to ensure proper mixing of the formulation. Extreme PR™ should be applied to the treatment area and gently massaged into the skin. The recommended frequency of application is up to four times daily.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that patients discontinue use and consult a healthcare professional if their condition worsens or persists for more than 7 days.

Warnings and Precautions

Contact with the eyes should be strictly avoided, as it may lead to irritation or injury. The product is intended for external use only and must not be applied to wounds or damaged skin to prevent adverse reactions.

Patients are advised to discontinue use and consult a healthcare professional if their condition worsens or persists for more than 7 days. This precaution is essential to ensure appropriate management and to rule out any underlying issues that may require further medical attention.

Side Effects

Patients should be advised to avoid contact with the eyes and to refrain from using the product on wounds or damaged skin, as it is intended for external use only.

In clinical practice, patients are instructed to stop using the product and consult a healthcare professional if their condition worsens or persists for more than 7 days. These precautions are essential to ensure the safe and effective use of 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 Bio-Scriptives Extreme Pr (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bio-Scriptives Extreme Pr.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of the reach of children. It is essential to ensure that the product is stored safely to prevent accidental ingestion or misuse.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

There is no specific information regarding the use of Bio-Scriptives Extreme PR - menthol lotion during pregnancy. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in women who are pregnant or may become pregnant. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes in the absence of established data.

Lactation

There are no specific warnings or recommendations regarding nursing mothers. Additionally, there are no specific considerations or precautions mentioned related to lactation. Therefore, healthcare professionals may consider the use of this medication in lactating mothers without specific concerns based on the available data.

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 maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

If available, specific antidotes or treatments should be administered as indicated based on the clinical scenario and the substance involved. Consultation with a poison control center or a medical toxicologist may also be beneficial in guiding the management of the overdose.

Documentation of the incident, including the substance involved, the amount ingested, and the time of ingestion, is crucial for effective 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 question.

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 the reach of children to prevent accidental ingestion or misuse.

Patients should be instructed to discontinue use and consult their healthcare provider if their condition worsens or persists for more than 7 days. This ensures that any potential complications are addressed promptly and appropriately.

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 ensure optimal stability. Freezing the product is not permitted, as it may compromise its effectiveness. Once opened, the product should be discarded after use to prevent any potential degradation or contamination.

Additional Clinical Information

Patients should apply and massage Extreme PR™ onto the treatment area up to four times daily. 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 Bio-Scriptives Extreme Pr, 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 Bio-Scriptives Extreme Pr, 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

Last AI update:

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.