ADD CONDITION

items per page

Kanjo Pain Relief Gel

Last content change checked dailysee data sync status

Active ingredient
Menthol 6 g/120 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2020
Label revision date
July 2, 2025
Active ingredient
Menthol 6 g/120 g
Other brand names
Dosage form
Gel
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2020
Label revision date
July 2, 2025
Manufacturer
CA-BOTANA INTERNATIONAL
Registration number
M017
NDC root
35192-039

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

Kanjo Pain Relief Gel is a topical treatment designed to help relieve pain in specific areas of your body. You apply a generous amount of the gel directly to the affected area and massage it into your skin until it is fully absorbed. This product is intended to provide localized pain relief, making it a convenient option for managing discomfort.

Uses

You can use this gel to help relieve pain in specific areas of your body. Simply apply a generous amount directly to the affected area and massage it into your skin until it is fully absorbed. This method allows the gel to work effectively where you need it most.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects associated with this gel. This makes it a safe option for pain relief without concerns about these specific risks.

Dosage and Administration

When using this topical massage gel, you can apply it directly to the skin where you feel discomfort. It’s important to use the gel no more than four times a day. This means you can spread out the applications throughout your day, but be sure not to exceed the recommended limit to ensure safety and effectiveness.

Simply massage a small amount of the gel into the affected area, and you should start to feel relief from pain or discomfort. Always remember to wash your hands after applying the gel to avoid getting it in your eyes or on other sensitive areas.

What to Avoid

It's important to be aware of certain guidelines when using this medication. If you notice any redness, irritation, or if your condition worsens, you should stop using the product and consult your doctor. Additionally, if your symptoms persist for more than 7 days or if they clear up and then return within a few days, it's crucial to seek medical advice.

Currently, there are no specific contraindications, controlled substance classifications, or noted risks of abuse or dependence associated with this medication. However, always prioritize your health and safety by following these instructions closely.

Side Effects

If you notice any redness or irritation while using this product, it's important to stop using it and consult your doctor. Additionally, if your symptoms worsen or do not improve after seven days, or if your symptoms seem to clear up only to return within a few days, seek medical advice.

Always keep this product out of reach of children. If it is swallowed, get medical help or contact a Poison Control Center immediately.

Warnings and Precautions

It's important to keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

You should stop using the product and consult your doctor if you notice any redness, irritation, or if your condition worsens. Additionally, if your symptoms last more than 7 days or clear up only to return within a few days, it's essential to reach out to your healthcare provider for further guidance.

Overdose

It's important to keep this medication out of reach of children. If a child accidentally swallows it, you should seek medical help or contact a Poison Control Center immediately.

In case of an overdose, you may notice signs such as unusual drowsiness, confusion, or difficulty breathing. If you or someone else experiences these symptoms, it's crucial to get medical assistance right away. Always prioritize safety and act quickly in these situations.

Pregnancy Use

The safety of this product during pregnancy has not been established, which means that it may not be safe for you or your developing baby. It is not recommended for use in pregnant women due to potential risks to the fetus (the unborn baby).

If you are pregnant or planning to become pregnant, it is important to consult your healthcare provider before using this product. They can help you understand the risks and make informed decisions about your health and the health of your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into breast milk, so caution is recommended.

The effects on your nursing infant have not been thoroughly studied, which means you should carefully weigh the potential risks against the benefits before making a decision. Your healthcare provider can help you navigate these considerations to ensure the best outcome for both you and your baby.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If your child accidentally swallows the product, seek medical help immediately or contact a Poison Control Center for guidance. Taking these precautions can help ensure your child's safety.

Geriatric Use

While there is no specific information available about the use of this medication in 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 wise to discuss any medications with a healthcare provider, especially since older adults may have different health needs and may be taking other medications.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health conditions and overall treatment goals. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

Renal Impairment

If you have kidney 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 usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect your treatment plan.

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 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 monitor your condition and make any necessary adjustments to your treatment plan.

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, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

To ensure the best performance of your product, it's important to store it in a cool, dry place. Protect it from excessive heat and direct sunlight, as these conditions can damage the product.

When handling the product, always do so with care to maintain its integrity. Following these simple guidelines will help ensure that your product remains safe and effective for use.

Additional Information

No further information is available.

FAQ

What is Kanjo Pain Relief Gel used for?

Kanjo Pain Relief Gel is used as an external topical analgesic. You should apply a generous amount directly to the affected area and massage it into the skin until thoroughly absorbed.

How often can I use Kanjo Pain Relief Gel?

You can use Kanjo Pain Relief Gel no more than four times daily.

Are there any contraindications for using this gel?

There are no contraindications listed for Kanjo Pain Relief Gel.

What should I do if I experience redness or irritation?

Stop using the gel and ask a doctor if redness is present, irritation develops, conditions worsen, or symptoms persist for more than 7 days.

Is Kanjo Pain Relief Gel safe to use during pregnancy?

The safety of Kanjo Pain Relief Gel during pregnancy has not been established, and it is not recommended for use in pregnant women due to potential risks to the fetus.

Can nursing mothers use Kanjo Pain Relief Gel?

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

What should I do if the product is swallowed?

Keep Kanjo Pain Relief Gel out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Are there any known drug interactions with Kanjo Pain Relief Gel?

No drug interactions have been mentioned for Kanjo Pain Relief Gel.

How should I store Kanjo Pain Relief Gel?

Protect Kanjo Pain Relief Gel from excessive heat and direct sunlight.

Packaging Info

Below are the non-prescription pack sizes of Kanjo Pain Relief Gel (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Kanjo Pain Relief Gel.
Details

Drug Information (PDF)

This file contains official product information for Kanjo Pain Relief Gel, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available data.

Uses and Indications

This drug is indicated for the topical treatment of localized pain. It is recommended to apply a generous amount of gel directly to the affected area and to massage it into the skin until thoroughly absorbed.

Limitations of Use: There are no known teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

The external topical analgesic should be applied as a massage gel to the affected area. The recommended dosing frequency is no more than four times daily. It is important to ensure that the gel is applied gently and evenly over the skin to maximize its analgesic effect. Healthcare professionals should advise patients to wash their hands after application, unless the hands are the area being treated.

Contraindications

There are no specific contraindications listed for this product. However, it is advised to discontinue use and consult a healthcare professional if any of the following occur: redness, irritation, worsening of conditions, or if symptoms persist for more than 7 days. Additionally, if symptoms resolve and then recur within a few days, medical advice should be sought.

Warnings and Precautions

It is imperative 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.

Healthcare professionals should instruct patients to discontinue use and consult a physician if any of the following occur: the presence of redness, the development of irritation, worsening of conditions, or if symptoms persist for more than 7 days. Additionally, if symptoms initially resolve and then recur within a few days, medical advice should be sought.

Side Effects

In clinical use, patients may experience a range of adverse reactions. Serious adverse reactions necessitate immediate medical attention. Patients should be advised to keep the product out of reach of children. In the event of accidental ingestion, it is crucial to seek medical help or contact a Poison Control Center without delay.

Common adverse reactions may include localized redness or irritation. Patients are instructed to discontinue use and consult a healthcare professional if redness is present, if irritation develops, or if conditions worsen or symptoms persist for more than seven days. Additionally, if symptoms resolve and then recur within a few days, patients should seek medical advice. These precautions are essential to ensure patient safety and effective management of any adverse effects.

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 Kanjo Pain Relief Gel (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Kanjo Pain Relief Gel.
Details

Pediatric Use

Pediatric patients should be advised to keep this product out of reach of children. In the event that the product is swallowed, it is crucial to seek medical assistance or contact a Poison Control Center immediately.

Geriatric Use

There is no specific information available 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

The safety of this product during pregnancy has not been established. It is not recommended for use in pregnant women due to potential risks to the fetus. Pregnant patients or those planning to become pregnant should consult a healthcare provider before using this product to discuss potential risks and benefits.

Lactation

Nursing 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. The effects on a nursing infant are not well studied; thus, the risks versus benefits should be considered.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in 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 event of an overdosage, it is imperative to keep the product out of reach of children. Should ingestion occur, immediate medical assistance is required. Healthcare professionals should advise caregivers to contact a Poison Control Center without delay.

Prompt action is crucial in managing potential overdosage situations to mitigate risks and ensure patient safety.

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 compound in these areas.

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.

Patients should be instructed to discontinue use and consult a doctor if they experience any redness, develop irritation, if their condition worsens, or if symptoms persist for more than 7 days. Additionally, patients should be made aware that if symptoms clear up and then recur within a few days, they should also seek medical advice.

Storage and Handling

This product is supplied in packaging that ensures its integrity during storage and handling. It is essential to protect the product from excessive heat and direct sunlight to maintain its efficacy and safety.

For optimal storage conditions, it is recommended to keep the product in a cool, dry place, away from sources of heat and light. Proper handling practices should be observed to prevent any degradation of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Kanjo Pain Relief Gel, 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 Kanjo Pain Relief Gel, 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.