Quality Choice Muscle and Joint

Description

QC Muscle and Joint Vanishing Scent Gel is a topical formulation designed for the relief of muscle and joint discomfort. The gel is characterized by its vanishing scent, which minimizes lingering odors associated with topical analgesics. It is formulated to provide targeted relief through a combination of active ingredients that penetrate the skin. The product is presented in a convenient gel dosage form, facilitating easy application and absorption.

Uses and Indications

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

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

Dosage and Administration

The product should be applied generously to the affected area, with gentle massage until the gel is fully absorbed. For optimal efficacy, this application should be repeated 3 to 4 times daily. The relief provided by the product is sustained for several hours.

To ensure maximum utilization of the product, it is recommended to squeeze the tube from the bottom and flatten it as the product is used. This technique aids in the effective dispensing of the gel.

Contraindications

There are no contraindications listed for this product. It is important to evaluate each patient's individual circumstances and medical history before prescribing.

Warnings and Precautions

For external use only. This product is contraindicated for use with heating pads, as the combination may lead to adverse effects. It is imperative that the product is not applied with tight bandaging, as this may exacerbate potential side effects or hinder proper absorption.

The product is not intended for ingestion. In the event of accidental swallowing, it is crucial to induce vomiting and seek immediate medical attention. Care should be taken to avoid contact with the eyes, mucous membranes, and any broken or irritated skin.

Should any redness or irritation occur, or if pain persists for more than 10 days, it is advised to discontinue use and consult a physician. Special caution is warranted for children under 12 years of age, particularly in the presence of arthritis-like conditions; in such cases, the product should not be used without medical guidance.

Side Effects

Patients should be aware that the product is for external use only and must not be used in conjunction with a heating pad. It is imperative to avoid tightly bandaging the area where the product is applied. The product is not intended for oral ingestion; if swallowed, patients should induce vomiting and seek medical attention immediately.

Care should be taken to keep the product away from the eyes, mucous membranes, and any broken or irritated skin. In the event that redness or irritation develops, or if pain persists for more than 10 days, particularly in cases involving arthritis-like conditions in children under 12 years of age, patients are advised to discontinue use and consult a physician.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding interactions between this medication and laboratory tests. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Quality Choice Muscle and Joint (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients should be monitored closely for any signs of redness or irritation. If such symptoms develop, or if pain persists for more than 10 days, or if arthritis-like conditions are observed in children under 12 years of age, the product should not be used, and a physician should be contacted immediately.

It is crucial to keep this product away from children to prevent accidental poisoning.

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

There is no specific information regarding the use of this drug 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 and the need to inform their healthcare provider if they become pregnant or plan to become pregnant while using this medication.

Lactation

There is no specific information regarding the use of this drug in lactating mothers or any lactation considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to nursing mothers, as the effects on breastfed infants are not established.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the lack of information necessitates careful clinical judgment and monitoring.

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 action is crucial. If the substance is ingested, it is recommended to induce vomiting as a first response. Following this, it is imperative to contact a physician for further evaluation and management.

Potential symptoms of overdosage may vary depending on the specific substance involved; therefore, healthcare professionals should remain vigilant for any signs of adverse reactions. Prompt medical intervention is essential to mitigate any potential complications associated with overdosage.

Healthcare providers are advised to follow established protocols for managing overdosage cases, which may include supportive care and symptomatic treatment as necessary. Continuous monitoring of the patient’s condition is recommended until they are stabilized.

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 poisoning. It is essential to emphasize the importance of proper storage and handling to ensure the safety of young children. Patients should be informed about the potential risks associated with accidental ingestion and encouraged to take necessary precautions.

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 within a temperature range of 15°C to 30°C (59°F to 86°F) to maintain its efficacy and stability. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable container that protects it from environmental factors. Special handling requirements should be observed to prevent any compromise to the product's integrity.

Additional Clinical Information

The product is administered topically, with a recommendation to apply the gel generously and massage gently until it disappears. This application should be repeated 3 to 4 times daily for optimal results.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Quality Choice Muscle and Joint, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)