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Foot Rehab Pain Relief and Moisturizer

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This product has been discontinued

Active ingredients
  • Menthol 8.5 g/85 g
  • Methyl Salicylate 12.75 g/85 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2012
Label revision date
February 12, 2013
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol 8.5 g/85 g
  • Methyl Salicylate 12.75 g/85 g
Other brand names
Dosage form
Cream
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 2012
Label revision date
February 12, 2013
Manufacturer
Mission Product Holdings
Registration number
part348
NDC root
76347-120
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

Foor Rehab™ is a topical product designed to provide pain relief and moisturization for your feet. It offers fast temporary relief from minor foot pain, making it a helpful option if you're experiencing discomfort. The non-greasy formula contains 10% menthol, which contributes to its soothing effects while also helping to keep your skin hydrated.

This dual-action product not only alleviates pain but also moisturizes, ensuring your feet feel comfortable and cared for. With a convenient size of 3 oz (85 g), it's easy to use whenever you need a little extra support for your feet.

Uses

If you're dealing with minor foot pain, this product can provide you with fast temporary relief. It works effectively to ease discomfort while also moisturizing your skin, making it a great choice for keeping your feet feeling good.

You can enjoy the benefits of both pain relief and hydration in one application, helping you stay comfortable throughout your day.

Dosage and Administration

It's important to use this medication only as directed by your healthcare provider. If you are an adult or a child aged 12 years or older, you can apply it to the affected area up to 3 to 4 times a day. Make sure to follow the recommended frequency to ensure safety and effectiveness.

If the patient is a child under 12 years old, it's best to consult a doctor before use. They can provide guidance on the appropriate dosage and application for younger patients. Always prioritize safety and follow the instructions provided by your healthcare professional.

What to Avoid

You should avoid using this product on wounds or damaged skin, as it may cause irritation or complications. Additionally, do not use it with a heating pad, as this can increase the risk of burns or other adverse effects. If you are considering using this product for a child under 12 years of age who has arthritis-like conditions, please refrain from doing so, as it is not recommended for that age group. Always prioritize safety and consult a healthcare professional if you have any questions or concerns.

Side Effects

It's important to be aware of some warnings associated with this product. It is meant for external use only, so you should avoid applying it to wounds or damaged skin. Additionally, do not use it in combination with a heating pad, and if you are considering using it on a child under 12 years old who has arthritis-like conditions, please consult a doctor first.

If you notice any redness over the area where you plan to apply the product, it's advisable to speak with a healthcare professional before proceeding. Your safety and well-being are paramount, so always take these precautions seriously.

Warnings and Precautions

This product is for external use only, so please avoid applying it to wounds or damaged skin. It should not be used with a heating pad or on children under 12 years old who have arthritis-like conditions. If you notice any redness in the area you plan to treat, consult your doctor before using the product.

If you accidentally swallow the product, seek medical help or contact a Poison Control Center right away. You should also stop using the product and call your doctor if your condition worsens, if symptoms last longer than 7 days, if symptoms improve and then return within a few days, or if you experience excessive skin irritation.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs or symptoms of an overdose for this medication, general signs can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or have concerns about a possible overdose, seek medical help right away. It's always better to err on the side of caution when it comes to your health. Remember, if you are ever in doubt, contacting a healthcare professional is the best course of action.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that the potential risks and benefits are not clearly defined.

If you are pregnant or planning to become pregnant, it’s important to discuss any medications you are considering with your healthcare provider. They can help you understand the best options for your health and the health of your baby. Always prioritize open communication with your doctor about any concerns you may have.

Lactation Use

If you are breastfeeding or planning to breastfeed, 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 about any medications you are taking to ensure they are safe for you and your baby. Your healthcare provider can give you personalized advice based on your unique situation.

Pediatric Use

It's important to keep this medication out of the reach of children to prevent accidental ingestion. If your child accidentally swallows it, seek medical help or contact a Poison Control Center right away.

For children under 12 years old, especially those with arthritis-like conditions, you should not use this medication without consulting a doctor first. Always check with a healthcare professional if you have any questions about using this medication for children under 12.

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 considering this medication, it’s important to consult with a healthcare provider. 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 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 should be used if you have hepatic impairment (issues with liver function).

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 you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always keep your healthcare team informed about all the medications and supplements you use, as well as any lab tests you may undergo. This way, they can provide the best care tailored to 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, please remember 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. This means you can put it directly on the skin where you need relief, but be careful not to exceed the recommended frequency. If you have any questions about how to use it or its effects, consult your healthcare provider for guidance.

FAQ

What is Foor Rehab™ used for?

Foor Rehab™ is used for fast temporary relief from minor foot pain and also acts as a moisturizer.

How should I use Foor Rehab™?

Apply Foor Rehab™ to the affected area not more than 3 to 4 times daily for adults and children 12 years of age or older. For children under 12, consult a doctor.

Are there any contraindications for using Foor Rehab™?

Do not use Foor Rehab™ on wounds or damaged skin, with a heating pad, or on a child under 12 years of age with arthritis-like conditions.

What should I do if I accidentally swallow Foor Rehab™?

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

What are the storage instructions for Foor Rehab™?

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

What should I do if my condition worsens while using Foor Rehab™?

Stop use and ask a doctor if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation occurs.

Is Foor Rehab™ safe to use during pregnancy or while nursing?

The provided information does not specify any warnings or recommendations regarding the use of Foor Rehab™ during pregnancy or lactation.

Packaging Info

Below are the non-prescription pack sizes of Foot Rehab Pain Relief and Moisturizer (menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Foot Rehab Pain Relief and Moisturizer.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Foor Rehab™ is a topical formulation designed for pain relief and moisturizing of the feet. It provides fast temporary relief from minor foot pain through its dual-action mechanism, combining effective pain relief with moisturizing properties. The product features a non-greasy formula that enhances user comfort. Each 3 oz (85 g) tube contains 10% menthol, which contributes to its analgesic effects.

Uses and Indications

This drug is indicated for the fast temporary relief of minor foot pain. It provides dual action by offering both pain relief and moisturizing benefits to the affected area.

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

Dosage and Administration

The medication should be used only 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 is contraindicated in the following situations:

The product should not be applied to wounds or damaged skin due to the risk of exacerbating the condition or causing further injury. Additionally, the use of this product in conjunction with a heating pad is contraindicated, as it may lead to increased risk of burns or skin irritation. Furthermore, it is not recommended for use in children under 12 years of age who present with arthritis-like conditions, as safety and efficacy have not been established in this population.

Warnings and Precautions

For external use only. This product should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad. It is contraindicated for use on children under 12 years of age who present with arthritis-like conditions. Healthcare professionals are advised to recommend that patients consult a physician prior to use if there is any redness present over the affected area.

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

Patients should be instructed to discontinue use and consult a healthcare provider if any of the following occur: the condition worsens or symptoms persist beyond 7 days; symptoms resolve only to reappear within a few days; or if excessive skin irritation develops.

Side Effects

Patients should be aware that the product is for external use only and should not be applied to wounds or damaged skin. Additionally, it should not be used in conjunction with a heating pad. The product is contraindicated for use in children under 12 years of age who have arthritis-like conditions.

Before using the product, patients are advised to consult a healthcare professional if there is any redness present over the affected area. These precautions are essential to ensure the safe and effective use of the product.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Foot Rehab Pain Relief and Moisturizer (menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Foot Rehab Pain Relief and Moisturizer.
Details

Pediatric Use

Pediatric patients should be kept out of the reach of children to prevent accidental ingestion. In the event of swallowing, immediate medical assistance or contact with a Poison Control Center is advised.

For children under 12 years of age, the use of this medication is not recommended for those with arthritis-like conditions. Additionally, it is important for caregivers to consult a healthcare professional before administering this medication to children under 12 years of age.

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 adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is no specific information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of effective contraception during treatment.

Lactation

There are no specific warnings or recommendations regarding nursing mothers or lactation in the provided text. Therefore, healthcare professionals should consider the absence of data when advising lactating mothers about the use of this medication. It is advisable to monitor breastfed infants for any potential effects, although no specific information is available regarding excretion in breast milk or effects on nursing infants.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data necessitates careful clinical judgment.

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 absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

If the substance involved is known, specific antidotes or treatments may be indicated, and healthcare professionals should refer to established guidelines for the management of overdose related to that substance.

In all cases, contacting a poison control center or a medical toxicologist for guidance is recommended to ensure appropriate management and intervention.

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.

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 the reach of children to prevent accidental ingestion. In the event of swallowing the medication, patients should seek medical assistance or contact a Poison Control Center immediately.

Patients should be instructed to stop using the medication and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, if symptoms resolve and then recur within a few days, or if excessive skin irritation occurs. It is important to emphasize that the medication is for external use only and should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad. Additionally, patients should be cautioned against using the medication on children under 12 years of age who have arthritis-like conditions.

Patients should be encouraged to consult a doctor before use if there is redness over the affected area. It is essential to use the medication only as directed. For adults and children aged 12 years and older, the medication should be applied to the affected area no more than 3 to 4 times daily. For children under 12 years of age, patients should be advised to seek a doctor's guidance before use.

Storage and Handling

The product is supplied in configurations that include 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 application to the affected area recommended no more than 3 to 4 times daily. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Foot Rehab Pain Relief and Moisturizer, 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 Foot Rehab Pain Relief and Moisturizer, 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

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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.