Feel Good Labs Natural Pain

Description

FEEL GOOD LABS NATURAL PAIN CREAM is presented in a dosage form of a topical cream, contained in a 100 ml tube. The product is designed for external application to provide relief from pain. The formulation includes a blend of natural ingredients, although specific inactive ingredients are not detailed in the provided information. The product is identified by the National Drug Code (NDC) 65121-260-00.

Uses and Indications

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

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

Dosage and Administration

For adults and children aged two years and older, the recommended application frequency is three to four times daily to the affected area. It is important to ensure that the application does not exceed this frequency to avoid potential adverse effects.

For children under two years of age, it is advised to consult a physician prior to use to determine the appropriate course of action and ensure safety.

Contraindications

The product is contraindicated for application to wounds or damaged skin due to the potential for irritation or adverse reactions. Additionally, it should not be used with tight bandaging, as this may compromise circulation and lead to further complications.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes to prevent irritation or injury. In the event that symptoms persist for more than seven days, the product should be discontinued, and a physician should be consulted for further evaluation and management.

In cases of accidental ingestion, it is essential to seek medical advice immediately. The product should not be applied to wounds or damaged skin, as this may exacerbate irritation or lead to complications. Additionally, care should be taken to avoid tight bandaging of the area where the product is applied, as this may hinder proper healing and increase the risk of adverse effects.

Healthcare professionals should advise patients who are pregnant or breastfeeding to consult with their physician prior to using this product to ensure safety for both the mother and child.

Side Effects

Patients using this product should be aware of several important warnings and precautions. The product is intended for external use only and should not come into contact with the eyes. In the event that symptoms persist for more than seven days, patients are advised to discontinue use and consult a physician.

It is crucial to keep the product out of reach of children. If swallowed, immediate consultation with a physician is recommended. Additionally, the product should not be applied to wounds or damaged skin, and it is advised not to bandage the area tightly after application.

For pregnant or breastfeeding individuals, it is essential to contact a physician prior to use to ensure safety and appropriateness of the product.

Drug Interactions

No specific drug interactions have been identified for this medication. Additionally, there are no reported interactions with laboratory tests. 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 Feel Good Labs Natural Pain (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients aged two years and older may apply the medication to the affected area no more than three to four times daily. For children under two years of age, it is recommended to consult a physician prior to use.

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

Pregnant patients and those who are breastfeeding should contact their physician prior to using this medication. It is essential to evaluate the potential risks and benefits in these populations to ensure the safety of both the mother and the fetus or infant.

Lactation

Lactating mothers are advised to contact their physician prior to using this medication. There is no available data regarding the excretion of this drug in human breast milk or its effects on breastfed infants. Therefore, healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating patients.

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. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this medication. 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 event of an overdosage, it is imperative that healthcare professionals take immediate action. If the product is ingested, the individual should be advised to consult a physician without delay.

Potential symptoms of overdosage may vary depending on the specific circumstances and the amount ingested. Therefore, a thorough assessment of the patient's condition is essential to determine the appropriate course of action.

Management of overdosage should be guided by clinical judgment and may include supportive care and symptomatic treatment as necessary. Continuous monitoring of the patient's vital signs and overall health status is recommended to ensure prompt intervention if complications arise.

Healthcare professionals are encouraged to report any cases of overdosage to the appropriate regulatory authorities to contribute to ongoing safety evaluations and risk management strategies.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients that if the medication is swallowed, it is important to consult a physician immediately. This guidance is crucial to ensure patient safety and to address any potential complications that may arise from improper use.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers assigned for identification. It is essential to store the product at room temperature to maintain its integrity and efficacy. No special handling requirements are noted; however, standard precautions should be observed to ensure optimal storage conditions.

Additional Clinical Information

Patients aged two years and older are advised to apply the medication to the affected area no more than three to four times daily. For children under two years of age, it is recommended that a physician be consulted prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Feel Good Labs Natural Pain, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)