Good Sense Pain Relief Roll on

Description

The product is a topical analgesic formulated for external use only. It contains active ingredients that provide pain relief, specifically targeting minor aches and pains associated with muscle and joint discomfort. The formulation is packaged in a roll-on applicator, facilitating easy application. Inactive ingredients include water, alcohol, and various botanical extracts.

Uses and Indications

This drug is indicated for the temporary relief of pain. There are no teratogenic or nonteratogenic effects mentioned associated with its use.

Dosage and Administration

For adults and children aged 12 years and older, the affected area should be cleaned prior to application. The product should be applied to the affected area no more than 3 to 4 times daily.

For children under 12 years of age, it is advised to consult a physician before use.

Contraindications

There are no specific contraindications associated with this product. However, it is essential to keep the product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, immediate medical assistance should be sought, or contact a Poison Control Center for guidance.

Warnings and Precautions

For external use only, this product is flammable and should be kept away from excessive heat or open flame. It is imperative to avoid using large quantities, particularly on raw surfaces or blistered areas, to prevent adverse effects.

When applying this product, care must be taken to avoid contact with the eyes. In the event of contact, the affected area should be rinsed with water immediately. This product should not be applied to wounds or damaged skin, and it is advised not to bandage the area tightly.

Healthcare professionals should instruct patients to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, if redness or irritation develops, medical consultation is recommended.

It is essential to keep this product out of reach of children. In cases where the product is ingested, immediate medical assistance should be sought, or contact with a Poison Control Center should be made without delay.

Side Effects

Patients should be aware that this product is intended for external use only. It is flammable; therefore, it must be kept away from excessive heat or open flame. Caution is advised to avoid using the product in large quantities, especially over raw surfaces or blistered areas.

During use, patients should take care to avoid contact with the eyes. In the event of contact, it is recommended to rinse the eyes with water. The product should not be applied to wounds or damaged skin, and it is advised not to bandage the area tightly.

Patients are instructed to discontinue use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, if redness or irritation develops, medical advice should be sought.

Drug Interactions

There are no specific drug interactions or laboratory test interactions identified in the available data. Therefore, no dosage adjustments or monitoring recommendations are necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Good Sense Pain Relief Roll on (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients aged 12 years and older may use the product by cleaning the affected area before application and applying it to the affected area no more than 3 to 4 times daily. For children under 12 years of age, it is advised to consult a doctor prior to use.

It is important to keep the product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

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

Pregnant patients should consult a healthcare professional prior to using this medication. The safety of this drug during pregnancy has not been established, and potential risks to fetal outcomes are not fully understood. Therefore, it is essential for women of childbearing potential to seek medical advice to weigh the benefits and risks before initiating treatment.

Lactation

Lactating mothers should consult a health professional before using this product. There is a potential for excretion in breast milk, and the effects on a nursing infant are not known.

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 and consider individual patient factors when prescribing to patients with reduced kidney function, as the absence of specific guidance necessitates careful clinical judgment.

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

If available, specific antidotes or treatments should be administered as indicated based on the clinical scenario and the substance involved. Continuous assessment and supportive care are critical in managing the patient's condition effectively.

Healthcare professionals are encouraged to report any cases of overdose to the appropriate regulatory authorities and to consult relevant toxicology resources for guidance on management protocols.

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.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the product out of reach of children to prevent accidental ingestion. It is important to emphasize that if the product is swallowed, patients should seek medical help or contact a Poison Control Center immediately. This information is crucial for ensuring patient safety and prompt action in case of an emergency.

Storage and Handling

The product is classified as flammable and should be kept away from excessive heat or open flame. It is recommended to store the product at room temperature. Additionally, it is important to keep the product out of reach of children. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The product is administered topically, with specific instructions for different age groups. Adults and children aged 12 years and older should clean the affected area before application and may apply the product no more than 3 to 4 times daily. For children under 12 years, it is advised to consult a doctor prior to use.

Clinicians should counsel patients on safety precautions, including the flammability of the product and the need to keep it away from excessive heat or open flames. Patients should avoid using large quantities, especially on raw surfaces or blistered areas, and should refrain from contact with eyes, rinsing with water if contact occurs. The product should not be applied to wounds or damaged skin, and tight bandaging is discouraged. Patients are advised to discontinue use and consult a doctor if the condition worsens, symptoms persist beyond 7 days, or if redness or irritation develops. It is crucial to keep the product out of reach of children, and immediate medical assistance should be sought if ingested. A health professional should be consulted before use.

Drug Information (PDF)

This file contains official product information for Good Sense Pain Relief Roll on, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)