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Green Compass Reduce Pain Relief with Menthol

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Active ingredient
Menthol, Unspecified Form 5 g/100 mL
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2023
Label revision date
January 1, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Menthol, Unspecified Form 5 g/100 mL
Other brand names
Dosage form
Gel
Route
Topical
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 2023
Label revision date
January 1, 2025
Manufacturer
Green Compass, Inc.
Registration number
M017
NDC root
73132-005
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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

REDUCE is a pain relief gel that contains menthol, designed to provide temporary relief from minor aches and pains in your muscles and joints. This product is formulated with 300 mg of CBG (cannabigerol), a compound derived from the cannabis plant, which may contribute to its soothing effects. Packaged conveniently as a roll-on, REDUCE is easy to apply and comes in a 2 fluid ounce (60 mL) bottle, making it a practical option for on-the-go relief.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It’s designed to help you feel more comfortable when dealing with these everyday discomforts.

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 who may be concerned about such risks.

Dosage and Administration

When using this medication, it's important to follow the directions provided. For adults and children aged 12 years and older, you should apply it to the affected area no more than 3 to 4 times a day. If the person using the medication is under 12 years old, it's best to consult a doctor for guidance on the appropriate use. Always ensure you are using the medication as directed for the best results.

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 could lead to irritation or other complications. Additionally, avoid using it in conjunction with a heating pad, as this may increase the risk of adverse effects.

By following these guidelines, you can help ensure a safe and effective experience with the product. If you have any questions or concerns, please consult with a healthcare professional.

Side Effects

When using this product, it's important to be aware of some key safety information. This product is for external use only, so avoid applying it to wounds or damaged skin, and do not use it with a heating pad. Be careful to keep it away from your eyes and avoid wrapping the area tightly with a bandage.

If your condition worsens, lasts more than seven days, or clears up only to return within a few days, stop using the product and consult a doctor. Additionally, keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only, so please avoid applying it to wounds or damaged skin, and do not use it with a heating pad. While using the product, be careful to keep it away from your eyes and avoid wrapping the area tightly with a bandage.

If your condition worsens, if symptoms persist for more than 7 days, or if the issue clears up and then returns within a few days, stop using the product and consult your doctor. Additionally, keep this product out of reach of children. If swallowed, seek 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 contact a Poison Control Center for guidance on what to do next.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to get help right away. Remember, acting quickly can make a significant difference in the outcome.

Pregnancy Use

When it comes to using this product during pregnancy, there is no specific information available in the drug insert. This means that there are no clear guidelines about whether the product is safe or poses any risks to you or your developing baby. Additionally, there are no recommendations for adjusting the dosage or taking special precautions while pregnant.

If you are pregnant or planning to become pregnant, it’s always best to consult with your healthcare provider before using any medication. They can help you weigh the potential benefits and risks based on your individual situation.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult with your healthcare professional before using this product. There is a possibility that the ingredients may be passed into your breast milk, so exercising caution is advised. Your healthcare provider can help you weigh the benefits and risks to ensure the safety of both you and your baby.

Pediatric Use

If your child is under 12 years old, it's important to consult with a doctor before using this medication. For those aged 12 and older, you can apply it to the affected area, but be sure not to exceed 3 to 4 applications in a day. Always follow these guidelines to ensure safe and effective use for your child.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it’s important to discuss any potential risks or concerns with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances. Always prioritize open communication with your doctor to ensure safe and effective treatment.

Renal Impairment

There are no specific guidelines, dosage adjustments, or monitoring requirements mentioned for patients with kidney problems in the provided information. If you have renal impairment (kidney issues), it's important to consult your healthcare provider for personalized advice regarding your treatment and any necessary precautions. Always keep them informed about your kidney health to ensure safe and effective medication management.

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 (liver issues).

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 have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This way, you can work together to ensure your treatment is safe and effective.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. This helps maintain its quality and performance. Before using the product, always check that the tamper evident seal is intact; do not use it if the seal is broken or missing, as this could indicate that the product has been compromised. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times daily if you are an adult or a child aged 12 years and older. If the patient is under 12 years old, it's important to consult a doctor before use. Always follow the guidance provided by your healthcare professional for the best results.

FAQ

What is REDUCE?

REDUCE is a pain relief gel that contains menthol and is designed for temporary relief of minor aches and pains of muscles and joints.

How should I use REDUCE?

You should apply REDUCE to the affected area not more than 3 to 4 times daily if you are an adult or a child 12 years of age and older. For children under 12, consult a doctor.

Are there any contraindications for using REDUCE?

There are no specific contraindications mentioned for REDUCE, but you should not use it on wounds or damaged skin or with a heating pad.

What should I do if my condition worsens while using REDUCE?

If your condition worsens, symptoms last more than 7 days, or if the condition clears up and occurs again within a few days, stop use and ask a doctor.

Is REDUCE safe to use during pregnancy?

The product insert does not provide specific information regarding the use of REDUCE during pregnancy, so consult a healthcare professional for advice.

Can nursing mothers use REDUCE?

Nursing mothers should consult a healthcare professional before using REDUCE, as there is a potential for excretion in breast milk.

What precautions should I take when using REDUCE?

When using REDUCE, avoid contact with the eyes and do not bandage tightly. Keep it out of reach of children, and if swallowed, seek medical help.

How should I store REDUCE?

Store REDUCE at room temperature and do not use it if the tamper evident seal is broken or missing.

Packaging Info

Below are the non-prescription pack sizes of Green Compass Reduce Pain Relief with Menthol (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Green Compass Reduce Pain Relief with Menthol.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

GREEN COMPASS REDUCE is a pain relief gel formulated with menthol, designed for topical application. Each 2 fluid ounce (60 mL) roll-on container contains 300 mg of cannabigerol (CBG). The product is intended for localized relief of discomfort.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles and joints.

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

Dosage and Administration

The medication should be used as directed. For adults and children aged 12 years and older, it is recommended to apply the product to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a physician before use.

Contraindications

Use of this product is contraindicated in the following situations:

Application on wounds or damaged skin is prohibited due to the potential for irritation and adverse effects. Additionally, the use of this product in conjunction with a heating pad is contraindicated, as it may lead to increased risk of skin irritation or burns.

Warnings and Precautions

For external use only. This product is contraindicated for application on wounds or damaged skin and should not be used in conjunction with a heating pad.

When utilizing this product, it is imperative to avoid contact with the eyes. Additionally, users should refrain from applying tight bandages over the treated area to prevent complications.

In the event that the condition worsens, symptoms persist beyond 7 days, or if the condition resolves and recurs within a few days, it is essential to discontinue use and consult a healthcare professional for further evaluation.

This product must be kept out of reach of children. In the case of accidental ingestion, immediate medical assistance should be sought, or contact should be made with a Poison Control Center.

Side Effects

Patients should be aware that this product is for external use only. It is contraindicated for use on wounds or damaged skin and should not be used in conjunction with a heating pad. While using this product, patients are advised to avoid contact with the eyes and to refrain from applying tight bandages.

In the event that the condition worsens, symptoms persist for more than 7 days, or if the condition clears up and recurs within a few days, patients should discontinue use and consult a healthcare professional. Additionally, this product should be kept out of reach of children. If swallowed, it is imperative to seek medical assistance or contact a Poison Control Center immediately.

Drug Interactions

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

Packaging & NDC

Below are the non-prescription pack sizes of Green Compass Reduce Pain Relief with Menthol (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Green Compass Reduce Pain Relief with Menthol.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a healthcare professional before use. For adolescents and children aged 12 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. Therefore, healthcare providers should exercise caution when prescribing this medication to geriatric patients. It is advisable to monitor these patients closely for any potential 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 this product during pregnancy provided in the drug insert. Additionally, there are no statements indicating whether the product is contraindicated in pregnancy or any associated risks to the fetus. As such, no dosage modifications or special precautions regarding use during pregnancy are mentioned. 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

Lactating mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk; therefore, caution is advised when administering to nursing mothers.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this drug. 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 overdosage, immediate medical assistance is essential. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help promptly or contact a Poison Control Center for guidance.

Symptoms of overdosage may vary depending on the specific substance involved. It is crucial for healthcare providers to assess the patient's condition and monitor for any adverse effects that may arise from the overdose.

Management of overdosage should be tailored to the individual case, taking into account the substance involved and the severity of symptoms. Healthcare professionals are encouraged to follow established protocols for the management of overdoses, which may include supportive care and symptomatic treatment as necessary.

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. Further studies may be necessary to elucidate these aspects of nonclinical toxicology.

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. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately.

Patients should be informed not to use the product on wounds or damaged skin, and they should avoid using it in conjunction with a heating pad. It is important to counsel patients to stop using the product and consult a doctor if their condition worsens or if symptoms persist for more than 7 days. Additionally, patients should be advised to seek medical advice if their condition improves and then recurs within a few days.

While using this product, patients must be cautioned to avoid contact with the eyes. Furthermore, they should be instructed not to bandage the area tightly when applying the product.

Storage and Handling

The product is supplied in a configuration that includes a tamper-evident seal. It is essential to store the product at room temperature to maintain its integrity and effectiveness. Healthcare professionals should ensure that the product is not used if the tamper-evident seal is broken or missing, as this may indicate potential contamination or compromise of the product.

Additional Clinical Information

The medication is administered topically, with the recommended frequency for adults and children aged 12 years and older being 3 to 4 applications to the affected area daily. For children under 12 years of age, it is advised to consult a doctor regarding the appropriate use. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Green Compass Reduce Pain Relief with Menthol, 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 Green Compass Reduce Pain Relief with Menthol, 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.