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Relieveit Footspray

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredient
Menthol 1.2 mg/15 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2020
Label revision date
March 13, 2020
Active ingredient
Menthol 1.2 mg/15 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2020
Label revision date
March 13, 2020
Manufacturer
Cosmetic Specialty labs, Inc.
Registration number
part348
NDC root
58133-956

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

You can use this medication for the temporary relief of minor aches and pains in your muscles, joints, and feet. It is designed to help alleviate discomfort, making it easier for you to go about your daily activities. If you're experiencing these types of pain, this drug may provide the relief you need.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles, joints, and feet. It’s designed to help you feel more comfortable when dealing with these everyday discomforts.

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

Dosage and Administration

To use this medication effectively, start by spraying it on the bare skin of your feet, including the arches, heels, toes, and legs, before you begin your day or any activities. You should apply 6 to 8 sprays on each foot. If you plan to wear stockings, make sure to apply it generously with at least 8 sprays on each foot for better coverage.

After spraying, allow the product to dry completely before putting on any footwear. If you find that you need more relief throughout the day, feel free to apply the spray again as needed. If you are considering using this product for a child under the age of 2, it’s important to consult a doctor first to ensure it’s safe for them.

What to Avoid

It's important to keep this medication out of reach of children to prevent accidental ingestion. If you or someone else swallows it, seek medical help immediately or contact a Poison Control Center for assistance.

There are no specific contraindications, controlled substance classifications, or noted risks of abuse, misuse, or dependence associated with this medication. However, always use it responsibly and follow any additional guidance from your healthcare provider.

Side Effects

When using this product, it's important to follow the directions carefully. It is meant for external use only, so avoid contact with your eyes or any mucous membranes. Do not apply it to open wounds, damaged skin, or very sensitive areas. If you have a known allergy to any of the ingredients in this product, you should not use it.

If you experience any adverse reactions, such as irritation or an allergic reaction, discontinue use immediately and consult a healthcare professional. Always prioritize your safety by using the product as intended.

Warnings and Precautions

This product is for external use only, so be sure to follow the directions carefully. Avoid getting it in your eyes or on sensitive areas, and do not apply it to open wounds or damaged skin. If you have any allergies to the ingredients in this product, do not use it.

If you are pregnant or breastfeeding, it's important to consult with a healthcare professional before using this product. Keep it out of reach of children, and if a child accidentally swallows it, seek 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 seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and get checked by a medical professional.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

If you have a child under the age of 2, it's important to consult a doctor before using this medication. This ensures that the treatment is safe and appropriate for your little one. Always prioritize your child's health by seeking professional advice when it comes to their medical care.

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 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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help monitor your liver function and make any necessary adjustments to your care.

Drug Interactions

It's great to know that there are no known interactions between this medication and other drugs or laboratory tests. However, it's still very important to discuss all medications you are taking, including over-the-counter drugs and supplements, with your healthcare provider. This ensures that your treatment is safe and effective.

Always keep your healthcare provider informed about any changes in your health or new medications you start. Open communication helps prevent any potential issues and supports your overall well-being.

Storage and Handling

It's important to handle and store your product safely to ensure its effectiveness. First, make sure not to use the product if the package seal is broken, as this could compromise its safety. For optimal storage, keep the product in a cool, dry place at a temperature between 68-77°F (20-25°C). This temperature range helps maintain the product's quality and effectiveness.

When handling the product, always ensure that your hands are clean to avoid contamination. Following these guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is the primary use of this drug?

This drug is used for temporary relief of minor aches and pains of muscles, joints, and feet.

Are there any teratogenic effects associated with this drug?

No teratogenic effects are mentioned for this drug.

How should I apply the spray?

You should spray 6-8 times on each foot, and apply generously (8+ sprays) when wearing stockings. Let it dry completely and apply again as needed for extended relief.

What precautions should I take when using this product?

Use only as directed, avoid contact with eyes or mucous membranes, and do not apply to open wounds or sensitive skin. Consult a doctor before use if you are pregnant, breastfeeding, or if the user is a child under 2.

What should I do if the product is swallowed?

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

Is there any information on drug interactions?

No drug interactions information is found for this product.

What should I do if the package seal is broken?

Do not use the product if the package seal is broken.

What is the recommended storage temperature for this drug?

Store the product at 68-77°F (20-25°C).

Packaging Info

Below are the non-prescription pack sizes of Relieveit Footspray (menthol 8%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Relieveit Footspray.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles, joints, and feet.

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

Dosage and Administration

Healthcare professionals should instruct patients to apply the product by spraying it on the bare skin of the feet, including the arches, heels, toes, and legs, prior to commencing daily activities. The recommended dosage is 6 to 8 sprays per foot. For individuals wearing stockings, a more generous application of 8 or more sprays per foot is advised.

It is essential that the product is allowed to dry completely before putting on footwear or stockings. Patients may reapply the product as needed for extended relief throughout the day.

For children under the age of 2, it is imperative to consult a healthcare provider before use to ensure safety and appropriateness of the treatment.

Contraindications

Use is contraindicated in children due to the risk of accidental ingestion. In the event of swallowing, immediate medical assistance should be sought or contact with a Poison Control Center is advised.

Warnings and Precautions

This product is intended for external use only. It is imperative that healthcare professionals advise patients to use the product strictly as directed. Care should be taken to avoid contact with the eyes and mucous membranes. The product should not be applied to open wounds, damaged skin, or areas of very sensitive skin. Additionally, individuals with known allergies to any of the active or inactive ingredients in this formulation should refrain from using the product.

For patients who are pregnant or breastfeeding, it is essential to consult a healthcare professional prior to use to ensure safety for both the mother and child.

To prevent accidental ingestion, the product must be kept out of reach of children. In the event of accidental swallowing, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

Patients should be aware that this product is for external use only. It is imperative to use the product strictly as directed. Contact with the eyes or mucous membranes should be avoided, and the product should not be applied to open wounds, damaged skin, or very sensitive areas. Additionally, individuals who are allergic to any of the active or inactive ingredients in this product should refrain from using it.

Failure to adhere to these warnings may result in adverse reactions, which could include irritation or allergic responses. It is essential for patients to follow these guidelines to minimize the risk of complications.

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 at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Relieveit Footspray (menthol 8%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Relieveit Footspray.
Details

Pediatric Use

Pediatric patients under 2 years of age should consult a healthcare professional prior to use. It is important to assess the appropriateness of treatment in this age group to ensure safety and efficacy.

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 prior to 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 currently 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 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, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. It is imperative that healthcare providers remain vigilant and prepared to address any complications that may arise from an overdosage scenario.

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 provided in the insert.

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 the safety and well-being of patients and their families.

Storage and Handling

The product is supplied in a package that must not be used if the seal is broken. It should be stored at a temperature range of 68-77°F (20-25°C) to ensure optimal stability and efficacy. Proper handling and storage conditions are essential to maintain the integrity of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Relieveit Footspray, 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 Relieveit Footspray, 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.