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Hemp Theory

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Menthol, Unspecified Form 2 mg/100 mL
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2019
Label revision date
December 9, 2019
Active ingredient
Menthol, Unspecified Form 2 mg/100 mL
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2019
Label revision date
December 9, 2019
Manufacturer
Clientele, Inc.
Registration number
part348
NDC root
64483-492

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Drug Overview

HEMP® THEORY is a fast-acting pain cream designed to provide temporary relief from minor aches and pains in muscles and joints. It contains 2400 mg of +NANO HEMP EXTRACT and nanobidiol®, which work together to help alleviate discomfort associated with conditions like arthritis, simple backache, strains, sprains, and bruises.

This cream comes in a 3 fl oz (89 ml) package, making it easy to apply when you need quick relief from everyday pain. Whether you're dealing with soreness from physical activity or chronic joint issues, HEMP® THEORY aims to support your comfort and mobility.

Uses

If you're dealing with minor aches and pains in your muscles and joints, this medication can help provide temporary relief. It's effective for discomfort associated with conditions like arthritis, simple backaches, strains, sprains, and bruises.

You can rely on this treatment to ease your pain and help you get back to your daily activities. Remember, it's designed for short-term use to manage these specific types of discomfort.

Dosage and Administration

If you are an adult or a child aged 2 years and older, you can apply this medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results.

For children under 2 years of age, it’s important to consult a physician (a medical doctor) before using this medication. This will help ensure safety and proper care for younger children.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. If you accidentally swallow it, seek medical help or contact a Poison Control Center immediately. This is crucial for your safety.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence (a condition where your body becomes reliant on a substance). However, always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

It's important to use this product only on the skin and avoid getting it in your eyes. If your condition worsens, or if symptoms last longer than 7 days or return after clearing up, you should stop using the product and consult a physician. Additionally, do not apply it to any wounds or damaged skin, and avoid wrapping the area tightly with a bandage.

Warnings and Precautions

This product is intended for external use only, so be sure to avoid getting it in your eyes. If your condition worsens, or if symptoms last longer than 7 days, or if they clear up and then return within a few days, stop using the product and consult your doctor. It's important not to apply it to wounds or damaged skin, and avoid wrapping the area tightly with a bandage.

Keep this product out of reach of children. If it is swallowed, seek medical help or contact a Poison Control Center immediately. Your safety is important, so please follow these guidelines carefully.

Overdose

If you or someone else has swallowed too much of this 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.

Signs of an overdose may include unusual symptoms, but specific details about these symptoms are not provided here. Always err on the side of caution and get help if you suspect an overdose has occurred. Your safety is the top priority, so don’t hesitate to reach out for assistance.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this product during pregnancy has not been evaluated. While there are no specific contraindications listed, caution is advised since the effects of topical menthol on pregnancy have not been established.

There is no detailed information available regarding potential risks to the fetus, and no dosage modifications are provided for pregnant individuals. It is highly recommended that you consult your physician before using this product to ensure it is safe for you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding nursing mothers or lactation in the information provided. This means that, based on the available data, there are no known risks associated with breastfeeding while using this medication. However, it's always a good idea to consult with your healthcare provider if you have any concerns or questions about your specific situation.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged 2 years and older, you can apply it to the affected area no more than 3 to 4 times a day. However, if your child is under 2 years old, you should consult a physician (a medical doctor) before using the product. This ensures that you are taking the right precautions for their safety and health.

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

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no guidelines, dosage adjustments, or monitoring instructions to share for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to discuss this with your healthcare provider for personalized advice and recommendations.

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, and there are no special monitoring or precautions outlined for patients with liver impairment.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe for your liver health. They can provide guidance tailored to your specific situation.

Drug Interactions

It's great to know that there are no identified interactions between this medication and other drugs or laboratory tests. This means that, in general, you can take this medication without worrying about it affecting other treatments or test results.

However, it's always important to discuss any medications you are taking or any upcoming lab tests with your healthcare provider. They can provide personalized advice and ensure that your treatment plan is safe and effective for you.

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. Once you open the product, be sure to discard it after use to maintain safety and quality. 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 a day if you are an adult or a child aged 2 years and older. If the patient is under 2 years old, it's important to consult a physician before use. There are no additional details available regarding laboratory tests, abuse potential, or postmarketing experiences related to this medication.

FAQ

What is HEMP® THEORY?

HEMP® THEORY is a fast-acting pain cream designed for the temporary relief of minor aches and pains in muscles and joints.

What conditions can HEMP® THEORY help relieve?

It can help relieve minor aches and pains associated with arthritis, simple backache, strains, sprains, and bruises.

How should I use HEMP® THEORY?

Apply to the affected area not more than 3 to 4 times daily for adults and children 2 years of age and older. Consult a physician for children under 2 years.

Are there any warnings for using HEMP® THEORY?

Yes, it is for external use only, should not contact the eyes, and should not be applied to wounds or damaged skin. If symptoms persist for more than 7 days, consult a physician.

Is HEMP® THEORY safe to use during pregnancy?

The product has not been evaluated for safety during pregnancy, so consult a physician if pregnant or planning to become pregnant before use.

What should I do if I swallow HEMP® THEORY?

If swallowed, get medical help or contact a Poison Control Center immediately.

How should I store HEMP® THEORY?

Store at room temperature, protect from light, and do not freeze. Discard after opening.

Are there any known drug interactions with HEMP® THEORY?

No drug interactions have been identified in the provided information.

Packaging Info

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

Packaging configurations for Hemp Theory.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

HEMP® THEORY Fast-Acting Pain Cream contains 2400 mg of nano hemp extract, specifically formulated with nanobidiol®. This topical dosage form is presented in a 3 fl oz (89 ml) container, designed for rapid absorption and effective relief. The product leverages advanced nanotechnology to enhance the bioavailability of its active ingredients.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of muscles and joints associated with various conditions, including arthritis, simple backache, strains, sprains, and bruises.

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

Dosage and Administration

For adults and children aged 2 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. It is important to ensure that the application is performed gently and that the area is clean prior to use.

For children under 2 years of age, it is advised to consult a physician before use to determine the appropriate course of action.

Contraindications

There are no contraindications listed for this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed.

Warnings and Precautions

For external use only; contact with the eyes should be avoided. In the event that the condition worsens, or if symptoms persist for more than 7 days or resolve and then recur within a few days, it is imperative to discontinue use of this product and consult a physician.

This product should not be applied to wounds or damaged skin. Additionally, it is important to avoid tight bandaging of the area where the product is applied.

To ensure safety, keep this product out of reach of children. In the case of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

Side Effects

Patients using this product should be aware that it is for external use only and must avoid contact with the eyes. In clinical practice, if the condition worsens, or if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days, it is advised to discontinue use and consult a physician.

Additionally, the product should not be applied to wounds or damaged skin, and it is important to avoid bandaging tightly over the area of application. These precautions are essential to ensure the safety and effectiveness of the treatment.

Drug Interactions

No drug interactions have been identified for the specified medication. Additionally, there are no interactions noted between the drug and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug interactions.

Packaging & NDC

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

Packaging configurations for Hemp Theory.
Details

Pediatric Use

Pediatric patients aged 2 years and older may apply the medication to the affected area no more than 3 to 4 times daily. For children under 2 years of age, it is recommended to consult a physician 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

The product has not been evaluated for safety during pregnancy. While specific contraindications are not mentioned, caution is advised as the safety of topical menthol during pregnancy has not been established. There is no specific information available regarding risks to the fetus. Additionally, no dosage modifications for pregnant individuals are provided. It is recommended that healthcare professionals advise patients to consult a physician if they are pregnant or planning to become pregnant before using this product.

Lactation

There are no specific warnings or recommendations regarding the use of this medication in nursing mothers. Additionally, there are no specific warnings or recommendations related to lactation. Healthcare professionals should consider the absence of data when advising lactating mothers about the use of this medication.

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

There is no information available regarding the use of this medication in patients with hepatic impairment. Consequently, there are no dosage adjustments, special monitoring requirements, or precautions specified for individuals with compromised liver function. Healthcare professionals should exercise clinical judgment when considering the use of this medication in patients with liver problems, as the absence of specific guidance necessitates careful evaluation of the patient's overall health status and liver function.

Overdosage

In the event of an overdosage, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment and monitoring of the patient are essential.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous evaluation and appropriate interventions should be implemented based on the clinical presentation and severity of symptoms.

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 the medication out of reach of children to prevent accidental ingestion. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact a Poison Control Center immediately. This guidance is crucial for ensuring patient safety and minimizing potential risks associated with accidental exposure.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Additionally, once opened, the product must be discarded to maintain safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3 to 4 times daily for adults and children aged 2 years and older. For children under 2 years of age, consultation with a physician is advised prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Hemp Theory, 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 Hemp Theory, 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.