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

Healthcare professionals are advised to apply the gel generously to the affected area, ensuring to gently massage until the gel is fully absorbed and disappears. This application should be repeated 3 to 4 times daily to achieve optimal relief, which can last for several hours. For best results, it is recommended to squeeze the tube from the bottom and flatten it as the product is used, ensuring efficient dispensing and minimizing waste.

Contraindications

Use is contraindicated in situations where there is a risk of accidental poisoning, particularly in children. It is essential to keep this product away from children to prevent potential harm. No other contraindications have been identified in the provided data.

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. It is imperative to avoid using the product in conjunction with a heating pad, as this may lead to adverse effects. Additionally, patients are advised not to bandage the area tightly after application, as this could exacerbate potential reactions.

In the event of accidental ingestion, it is crucial to induce vomiting and seek medical attention immediately. The product should be kept away from the eyes, mucous membranes, and any broken or irritated skin. Should any redness or irritation develop, or if pain persists for more than 10 days, particularly in cases involving arthritis-like conditions in children under 12 years of age, the product should be discontinued, and a physician should be consulted.

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 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 information available regarding the use of this drug during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential risks and benefits. Women of childbearing potential should be counseled on the absence of information related to pregnancy and the importance of discussing any plans for pregnancy or potential exposure during treatment.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. Further research may be necessary to fully understand the implications for breastfed infants.

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 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 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 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 container requirements should be adhered to, ensuring that the product is kept in a suitable environment. Special handling needs must be observed to prevent any compromise to the product's integrity during storage and transportation.

Additional Clinical Information

The medication is administered topically, with patients advised to apply the gel generously and gently massage until it disappears. This application should be repeated 3 to 4 times daily to ensure optimal efficacy.

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)