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Pain Relief

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This product has been discontinued

Active ingredients
  • Menthol, Unspecified Form 78 mg
  • Camphor (synthetic) 78 mg
  • Methyl Salicylate 78 mg
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2019
Label revision date
January 12, 2021
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol, Unspecified Form 78 mg
  • Camphor (synthetic) 78 mg
  • Methyl Salicylate 78 mg
Other brand names
Dosage form
Patch
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 2019
Label revision date
January 12, 2021
Manufacturer
Unexo Life Sciences, Private Limited
Registration number
part348
NDC root
71391-135
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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

unexo® is a medicated pain relief patch designed to provide fast-acting relief for minor aches and pains in muscles and joints. It is particularly useful for conditions such as simple backache, arthritis, sprains, strains, and bruises. You can apply the patch to areas like your lower back, joints, upper back, shoulder, or elbow for a duration of 8 to 12 hours, helping to alleviate discomfort effectively.

This product comes in a package of three large patches, making it convenient for ongoing use as needed.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is effective for conditions such as simple backache, arthritis, sprains, strains, and bruises. If you're experiencing discomfort from any of these issues, this medication may help alleviate your pain and improve your mobility.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can use this medication by applying it directly to the affected area of your skin. Make sure to dry the skin completely before applying the patch. You should only apply the patch up to two times a day.

To use the patch, first open the pouch and carefully remove the patch. Peel off the protective film and place the sticky side onto the affected area. If you need to apply it on hairy skin, gently remove the patch using mild warm water. Remember, once you have used a patch, it cannot be reapplied or reused, so be sure to dispose of it properly after use. If you are considering this treatment for a child under 12 years old, please consult a doctor first.

What to Avoid

It's important to use this product safely. You should avoid applying it to open wounds, cuts, your eyes, or your face, as these areas can be sensitive and may react negatively. Additionally, do not use it in combination with a heating pad, as this could lead to unwanted effects.

While there are no specific contraindications or concerns about abuse, misuse, or dependence mentioned, always prioritize your safety and follow these guidelines to ensure the best experience with the product.

Side Effects

When using this product, it's important to be aware of potential side effects and safety precautions. You should avoid applying it to open wounds, cuts, or sensitive areas like your eyes and face. If you experience any redness over the affected area, have sensitive skin, or are pregnant or breastfeeding, consult your doctor before use.

If your condition worsens, symptoms persist for more than 7 days, or if you notice abnormal skin irritation after using the product, stop using it and seek medical advice. Always keep the product out of reach of children, and if swallowed, contact a Poison Control Center or seek medical help immediately.

Warnings and Precautions

This product is for external use only, so please use it exactly as directed. Avoid applying it to open wounds, cuts, your eyes, or face, and do not use it with a heating pad. While using this product, be careful to keep it away from your eyes and mucous membranes, and avoid wrapping the area tightly with bandages.

Before using this product, consult your doctor if you notice redness in the affected area, have sensitive skin, or are pregnant or breastfeeding. If your condition worsens, symptoms last more than 7 days, or if you experience abnormal skin irritation, stop using the product and contact your doctor.

If you accidentally swallow the product, seek emergency 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 act quickly. Seek medical help immediately or contact a Poison Control Center for guidance.

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. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult your doctor before using this medication. Your healthcare provider can help you understand any potential risks and ensure that you make the safest choices for you and your baby. Always prioritize open communication with your doctor regarding your health during this time.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult your doctor before using any medication. This is to ensure that it is safe for you and your baby. Your healthcare provider can help you understand any potential risks and make informed decisions about your health and your baby's well-being. Always prioritize open communication with your doctor regarding your breastfeeding status when considering new treatments.

Pediatric Use

This medication is approved for use in adults and children who are 12 years old and older. If your child is younger than 12, it’s important to consult a doctor before giving them this medication. Always ensure you follow your healthcare provider's guidance regarding dosage and safety for your child.

Geriatric Use

This medication is intended for use by adults and children aged 12 years and older. If you are caring for a child under 12, it’s important to consult a doctor before giving them this medication.

As you consider treatment options for older adults, remember that their needs may differ from those of younger individuals. Always discuss any concerns or questions with a healthcare provider to ensure safe and effective use.

Renal Impairment

If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help monitor your kidney function and make any necessary adjustments to 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).

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 best performance and safety of your product, store it at room temperature, keeping it below 80°F (27°C). This temperature range helps maintain the integrity of the device.

When handling the product, always do so with clean hands and in a clean environment to avoid contamination. If you have any specific disposal instructions, be sure to follow them carefully to ensure safe and responsible disposal.

Additional Information

You should apply this medication topically to the affected area, but no more than twice a day. Before using it, consult your doctor if you have redness in the area, sensitive skin, or if you are pregnant or breastfeeding.

If your condition worsens, symptoms last longer than 7 days, or if they clear up and then return within a few days, stop using the medication and contact your doctor. Additionally, if you experience any unusual skin irritation after using the product, seek medical advice.

FAQ

What is unexo®?

Unexo® is a medicated pain relief patch that provides fast-acting relief for minor aches and pains of muscles and joints.

What conditions can unexo® help with?

Unexo® is indicated for temporary relief of minor aches and pains associated with simple backache, arthritis, sprains, strains, and bruises.

How do I use unexo®?

Apply the patch to the affected area for 8-12 hours, no more than twice a day. Ensure the skin is dry before application.

Who can use unexo®?

Unexo® is for use by adults and children 12 years of age and older. Consult a doctor for children under 12.

Are there any warnings for using unexo®?

Yes, unexo® is for external use only. Do not use on open wounds, cuts, eyes, or face, and avoid using with a heating pad.

What should I do if I experience irritation?

Stop using unexo® and consult your doctor if the condition worsens, symptoms persist for more than 7 days, or if abnormal skin irritation occurs.

What should I do if unexo® is swallowed?

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

How should I store unexo®?

Store unexo® at room temperature below 80°F (27°C).

Can I use unexo® if I am pregnant or breastfeeding?

Consult your doctor before using unexo® if you are pregnant or breastfeeding.

Packaging Info

Below are the non-prescription pack sizes of Pain Relief (menthol, unspecified form, methyl salicylate, and camphor (synthetic)). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Pain Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

unexo® is a medicated pain relief patch developed by LIFE SCIENCES, designed for the management of pain in various areas including the lower back, joints, upper back, shoulder, and elbow. Each patch is formulated for fast-acting relief and is intended for application for a duration of 8 to 12 hours. The product is available in a large size and is packaged with three patches per unit. It is recommended to reseal the package after opening to maintain product integrity. The National Drug Code (NDC) for unexo® is 71391-135-03.

Uses and Indications

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

There are no teratogenic or nonteratogenic effects mentioned in the available data.

Dosage and Administration

For adults and children aged 12 years and older, the patch should be applied to the affected area no more than twice daily. Prior to application, ensure that the skin in the application area is completely dry.

To apply the patch, open the pouch and remove the patch. Peel off the protective film and apply the sticky side directly to the affected area. In cases where the patch is to be applied on hairy skin, it is recommended to remove the hair gently using mild warm water to facilitate adhesion.

Once the patch has been used, it cannot be re-pasted or reused. Proper disposal of the patch after use is essential. For children under 12 years of age, consultation with a healthcare professional is advised before use.

Contraindications

The product is contraindicated for use on open wounds, cuts, eyes, and the face due to the potential for irritation and adverse reactions. Additionally, the use of this product in conjunction with a heating pad is contraindicated, as it may increase the risk of skin irritation or burns.

Warnings and Precautions

For external use only, this product must be utilized strictly as directed. It is imperative to avoid application on open wounds, cuts, the eyes, and the face. Additionally, the use of a heating pad in conjunction with this product is contraindicated.

When using this product, care should be taken to prevent contact with the eyes and mucous membranes. Bandaging should not be applied tightly to the treated area to avoid complications.

Healthcare professionals should advise patients to consult a physician prior to use if they experience redness over the affected area, have sensitive skin, or are pregnant or breastfeeding.

Patients are instructed to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Furthermore, if any abnormal skin irritation occurs following application, medical consultation is recommended.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

Patients using this product should be aware of several important warnings and precautions. This product is intended for external use only and should not be used otherwise than as directed. It is contraindicated for application on open wounds, cuts, the eyes, and the face, and should not be used in conjunction with a heating pad.

While using this product, patients should avoid contact with the eyes and mucous membranes and should not apply a tight bandage over the treated area. Individuals with redness over the affected area, sensitive skin, or those who are pregnant or breastfeeding should consult a healthcare professional before use.

Patients are advised to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, if abnormal skin irritation occurs after usage, medical consultation is recommended.

It is crucial to keep this product out of reach of children. In the event of accidental ingestion, patients should seek medical help 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 Pain Relief (menthol, unspecified form, methyl salicylate, and camphor (synthetic)). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Pain Relief.
Details

Pediatric Use

Pediatric patients aged 12 years and older may use this medication. For children under 12 years of age, it is advised to consult a healthcare professional before use.

Geriatric Use

Elderly patients, defined as those 65 years of age and older, may require careful consideration when prescribing this medication. While the medication is indicated for use in adults and children aged 12 years and older, specific dosage adjustments or safety considerations for geriatric patients have not been explicitly detailed in the prescribing information.

Healthcare providers should exercise caution when administering this medication to elderly patients, as they may have altered pharmacokinetics and pharmacodynamics. It is advisable to monitor these patients closely for any adverse effects or changes in therapeutic response. Additionally, given the lack of data regarding the safety and efficacy of this medication in patients under 12 years of age, consultation with a healthcare professional is recommended for this population.

In summary, while the medication is suitable for adults and children aged 12 and older, special attention should be given to elderly patients to ensure safe and effective use.

Pregnancy

Pregnant patients and those who are breastfeeding should consult their healthcare provider before using this medication. The potential risks and benefits must be carefully considered in these populations. There is limited data available regarding the safety of this medication during pregnancy and lactation, and therefore, healthcare professionals are advised to evaluate the individual circumstances of each patient.

Lactation

Lactating mothers are advised to consult their healthcare provider prior to using this medication if they are breastfeeding. There is no specific data available regarding the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, healthcare professionals should consider the potential risks and benefits when recommending this medication to lactating mothers.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the drug insert regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to 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 prescribing information.

Overdosage

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

Prompt action is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous monitoring and evaluation are recommended to ensure patient safety and effective resolution of any complications arising from the overdosage.

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 provided text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. 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 open wounds, cuts, or on the eyes and face. Additionally, it is important to caution against using the product in conjunction with a heating pad, as this may lead to adverse effects.

Healthcare providers should encourage patients to stop using the product and consult their doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Patients should also be advised to discontinue use and seek medical advice if they experience any abnormal skin irritation following application.

While using the product, patients must be reminded to avoid contact with their eyes and mucous membranes. They should also be instructed not to bandage the area tightly after application.

Before using the product, patients should be encouraged to consult their doctor if they have redness over the affected area, have sensitive skin, or are pregnant or breastfeeding. This ensures that any potential risks are adequately assessed prior to use.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product at room temperature, ensuring that the temperature does not exceed 80°F (27°C). Proper storage conditions are crucial to maintain the integrity and efficacy of the product.

Additional Clinical Information

The medication is administered topically, with a recommended application to the affected area no more than twice daily. Clinicians should counsel patients to consult their doctor prior to use if they experience redness over the affected area, have sensitive skin, or are pregnant or breastfeeding. Patients are advised to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than seven days, or if abnormal skin irritation occurs after application.

Drug Information (PDF)

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