ADD CONDITION

items per page

Cannarelief 1000mg

Last content change checked dailysee data sync status

Active ingredient
Menthol 7.9 g/71.9 g
Other brand names
Dosage form
Salve
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2023
Label revision date
January 15, 2025
Active ingredient
Menthol 7.9 g/71.9 g
Other brand names
Dosage form
Salve
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 15, 2025
Manufacturer
Carolina Cannabis Creations LLC
Registration number
M017
NDC root
82876-010

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

CannaRelief 1000mg CBD is a product designed to provide temporary relief from various types of discomfort, including aches and pains related to arthritis, backache, joint pain, and muscle strains or sprains. It is formulated to help ease these common issues, making it a supportive option for those seeking comfort from everyday physical discomfort.

While the specific mechanism of action is not detailed, CannaRelief is part of a growing category of products that utilize CBD (cannabidiol), a compound derived from the cannabis plant, known for its potential therapeutic properties. If you're looking for a natural approach to managing pain, CannaRelief may be worth considering.

Uses

If you're dealing with temporary aches and pains, this medication can help provide relief. It's effective for discomfort related to arthritis, backaches, joint pain, muscle strains, and sprains. Whether you're recovering from an injury or managing chronic pain, this option may ease your symptoms and improve your comfort.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer choice for those concerned about such risks.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can apply the medication to the affected area one to four times a day, depending on your needs. Make sure to follow the instructions carefully to ensure the best results.

For children under 12 years old, it’s important to consult a doctor before using this medication. They can provide guidance on the appropriate use and dosage for younger patients. Always prioritize safety and follow professional advice when it comes to medication for children.

What to Avoid

It's important to use this medication safely. You should not apply it to wounds or irritated skin, as this can lead to complications. Additionally, make sure to avoid contact with your eyes to prevent irritation or injury.

While there are no specific contraindications or concerns about abuse, misuse, or dependence associated with this medication, following these guidelines will help ensure your safety and the effectiveness of the treatment. Always consult with your healthcare provider if you have any questions or concerns.

Side Effects

You should be aware that this product is for external use only and is designed to provide penetrating pain relief. If your condition worsens, if symptoms last more than 7 days, or if the condition clears but then returns within a few days, it’s important to stop using the product and consult a doctor. Additionally, if you experience any rash or irritation, you should also seek medical advice.

Keep an eye on your symptoms and don’t hesitate to reach out for help if you notice any of these issues. Your health and safety are important.

Warnings and Precautions

This medication is for external use only and is designed to provide penetrating pain relief. It's important to avoid applying it to any wounds or irritated skin, and you should keep it away from your eyes to prevent irritation.

If your condition worsens, if symptoms last more than 7 days, or if the condition seems to clear up but then comes back within a few days, you should stop using the medication and call your doctor. Additionally, if you experience any rash or irritation, discontinue use and consult your healthcare provider.

Overdose

If you suspect an overdose, it’s crucial to seek medical help immediately or contact a poison control center. Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing.

Don’t wait for symptoms to worsen; getting prompt assistance can be vital. Always prioritize your safety and the safety of others by acting quickly in these situations.

Pregnancy Use

If you are pregnant or breastfeeding, it is important to consult a health professional before using this medication. They can provide guidance tailored to your specific situation and help ensure the safety of both you and your baby. Always prioritize open communication with your healthcare provider regarding any medications you may be considering during this time.

Lactation Use

If you are pregnant or breastfeeding, it’s important to talk to your healthcare provider before using any medication. They can help you understand the potential risks and benefits, ensuring the safety of both you and your baby. Always prioritize open communication with your doctor to make informed decisions about your health while nursing.

Pediatric Use

If your child is 12 years old or younger, it's important to consult a doctor before using this medication. For those aged 12 and older, you can apply it to the affected area one to four times a day as needed. Always remember to keep this medication out of reach of children to ensure their safety.

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 before starting the medication. 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, especially if you have concerns about your kidney health. They can provide guidance based on your individual situation.

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).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help you understand how to manage your treatment effectively.

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 interactions with other drugs or laboratory tests. However, your healthcare provider can help ensure that your treatment plan is safe and effective, taking into account your unique health needs.

Always feel free to ask questions and share any concerns you have about your medications or tests. This way, you can work together to make informed decisions about your health.

Storage and Handling

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

When handling the product, make sure to maintain a clean environment to prevent contamination. Following these simple storage and handling guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is CannaRelief 1000mg CBD used for?

CannaRelief 1000mg CBD is used for temporary relief of aches and pains associated with arthritis, backache, joint pain, muscle strains, and sprains.

How should I use CannaRelief 1000mg CBD?

Adults and children 12 years and over should apply it to the affected area one to four times daily. For children 12 years and younger, consult a doctor.

Are there any warnings for using CannaRelief 1000mg CBD?

Yes, it is for external use only and provides penetrating pain relief. Avoid applying it to wounds or irritated skin and keep it away from your eyes.

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

Stop use and ask a doctor if your condition worsens, symptoms last more than 7 days, or if a rash or irritation occurs.

Can I use CannaRelief 1000mg CBD if I am pregnant or breastfeeding?

Consult a health professional before using CannaRelief if you are pregnant or breastfeeding.

What should I do if I accidentally apply CannaRelief to my eyes?

Avoid contact with eyes. If contact occurs, rinse thoroughly with water and seek medical advice if irritation persists.

How should I store CannaRelief 1000mg CBD?

Store it at 68-77 degrees Fahrenheit and avoid direct sunlight.

Packaging Info

Below are the non-prescription pack sizes of Cannarelief 1000mg (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cannarelief 1000mg.
Details

Drug Information (PDF)

This file contains official product information for Cannarelief 1000mg, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

CannaRelief 1000mg CBD is a liquid formulation containing cannabidiol (CBD) derived from hemp. Each 1 mL of the product delivers 33.33 mg of CBD. The inactive ingredients consist of medium-chain triglyceride (MCT) oil and natural flavoring. CannaRelief is packaged in a 30 mL bottle. The SPL code for this product is 34089-3.

Uses and Indications

This drug is indicated for the temporary relief of aches and pains associated with arthritis, backache, joint pain, muscle strains, and sprains.

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

Dosage and Administration

For adults and children aged 12 years and over, the recommended application is to the affected area one to four times daily, depending on the severity of the condition. For children under 12 years of age, it is advised to consult a physician prior to use to determine the appropriate course of action.

Contraindications

The product should not be applied to wounds or irritated skin, as this may exacerbate the condition or lead to adverse effects. Additionally, contact with the eyes must be avoided to prevent irritation or injury.

Warnings and Precautions

FOR EXTERNAL USE ONLY. This product is designed to provide penetrating pain relief.

Healthcare professionals should advise patients to discontinue use and consult a physician if any of the following occur: the condition worsens, symptoms persist for more than 7 days, the condition resolves but recurs within a few days, or if a rash or irritation develops.

It is crucial to emphasize general precautions to patients. The product should not be applied to open wounds or irritated skin, and care should be taken to avoid contact with the eyes to prevent adverse effects.

No specific laboratory tests are recommended for monitoring during the use of this product. However, ongoing assessment of the patient's condition is advised to ensure safety and efficacy.

Side Effects

Patients using this product should be aware that it is intended for external use only and is designed to provide penetrating pain relief.

In clinical practice, participants are advised to stop use and consult a healthcare professional if the condition worsens, if symptoms persist for more than 7 days, or if the condition appears to resolve but recurs within a few days. Additionally, the occurrence of a rash or irritation necessitates discontinuation of use and medical consultation.

It is important to note that worsening of the condition, prolonged symptoms, recurrence of the condition, and the development of rash or irritation are significant adverse reactions that may arise during treatment. These reactions should be monitored closely to ensure patient safety and effective management of symptoms.

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified for this product. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary.

Packaging & NDC

Below are the non-prescription pack sizes of Cannarelief 1000mg (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Cannarelief 1000mg.
Details

Pediatric Use

Pediatric patients 12 years and younger should consult a healthcare professional before use. For patients aged 12 years and older, the recommended application is to the affected area one to four times daily. It is important to keep this product out of reach of children to ensure safety.

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

Pregnant patients and those who are breastfeeding should consult a healthcare professional before 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 no available data regarding the excretion of this medication 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 the use of this medication. 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 available information.

Overdosage

In the event of an overdosage, it is imperative to seek immediate medical assistance or contact a poison control center. Prompt intervention is crucial to mitigate potential adverse effects associated with the overdosage.

Healthcare professionals should be aware that symptoms of overdosage may vary depending on the specific substance involved. Therefore, a thorough assessment of the patient's condition is essential.

Management of overdosage typically involves supportive care and symptomatic treatment. Continuous monitoring of the patient's vital signs and clinical status is recommended. In cases where specific antidotes are available, their administration should be considered based on the clinical scenario.

It is vital for healthcare providers to remain vigilant and act swiftly to ensure the safety and well-being of the patient experiencing an overdosage.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

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 reach of children to prevent accidental ingestion or misuse.

Patients should be instructed not to apply the medication to wounds or irritated skin and to avoid contact with the eyes, as this may lead to adverse effects.

Additionally, healthcare providers should counsel patients to monitor their condition closely. They should seek medical advice if the condition worsens, if symptoms persist for more than 7 days, if the condition appears to clear but recurs within a few days, or if any rash or irritation develops.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available upon request. It is essential to store the product at a temperature range of 68 to 77 degrees Fahrenheit. Care should be taken to avoid direct sunlight during storage to maintain product integrity.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Cannarelief 1000mg, 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 Cannarelief 1000mg, 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.