Natures Sunshine Products

Description

Everflex Topical Analgesic Pain Relief Cream is formulated with Methylsulfonylmethane (MSM) as an active ingredient. This topical analgesic is presented in a cream dosage form, packaged in a 2-ounce (57 grams) container. The product is designed for localized pain relief.

Uses and Indications

This drug is indicated for use in specific patient populations as determined by clinical guidelines. Currently, there are no detailed indications or usage specifications provided. Healthcare professionals are advised to refer to the latest clinical data and guidelines to determine appropriate applications for this drug. There are no known teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

Healthcare professionals are advised to instruct patients to massage Everflex into the affected areas. The recommended frequency of application is three to four times per day. It is important to ensure that the product is applied gently and thoroughly to maximize its efficacy in alleviating discomfort.

Contraindications

Use of this product is contraindicated in children due to the risk of accidental ingestion. It should be kept out of reach of children to prevent potential harm. No other contraindications have been identified.

Warnings and Precautions

The product is intended for external use only. It is imperative that healthcare professionals advise patients to avoid contact with the eyes to prevent potential irritation or adverse effects.

In addition, it is recommended that healthcare providers monitor patients for any signs of local reactions or sensitivities following application. Regular assessment of the treatment area may be necessary to ensure safety and efficacy.

Side Effects

Patients should be advised that the product is for external use only and must be kept away from the eyes to prevent irritation or injury. There are no additional specific adverse reactions reported in clinical trials or postmarketing experiences beyond these warnings. It is essential for participants to adhere to these guidelines to ensure safe usage of the product.

Drug Interactions

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

Packaging & NDC

Below are the non-prescription pack sizes of Natures Sunshine Products (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients should be advised to keep the product out of reach of children. In cases where the condition worsens, or if symptoms persist for more than 7 days or resolve and then recur within a few days, the product should be discontinued, and a physician should be consulted.

The product is intended for external use only and should not be applied to wounds or damaged skin. Additionally, it is important to avoid tight bandaging of the area where the product is applied. Care should be taken to prevent contact with the eyes.

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.

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 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 implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the substance involved, estimated dose, and time of exposure, is crucial for effective management and follow-up care.

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. Further studies may be necessary to elucidate these aspects of nonclinical toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage and handling to ensure the safety of young individuals.

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 in a cool, dry place to maintain its integrity and effectiveness. Proper storage conditions are crucial to ensure the product remains within its specified temperature range and is protected from moisture.

Additional Clinical Information

The product is administered topically, with directions for use indicating that it should be massaged into painful areas 3 to 4 times per day. Clinicians should advise patients to keep the product out of reach of children and to discontinue use if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. It is important to instruct patients not to apply the product to wounds or damaged skin, to avoid tight bandaging, and to use it for external purposes only. Additionally, patients should be cautioned to avoid contact with the eyes.

Drug Information (PDF)

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

View product document (PDF)