Natural Relief 1222

Description

The provided data does not specify the chemical name, physical characteristics, or inactive ingredients of the drug. Therefore, a detailed description cannot be formulated based on the available information. Further details are required to create a comprehensive description.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with various conditions, including arthritis, simple backache, muscle strains, sprains, and bruises.

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

Dosage and Administration

Adults and children 12 years of age and older should apply the product liberally to the affected area. The application should be followed by gentle massage into the painful area until the formulation is thoroughly absorbed into the skin. This process may be repeated as necessary to achieve the desired effect.

The product is intended for topical application. It is important to ensure that the method of administration involves massaging the formulation into the skin, allowing for optimal absorption and efficacy.

Contraindications

The product is contraindicated in the following situations:

Tight bandaging should be avoided to prevent compromised circulation. Contact with the eyes must be avoided to prevent irritation or injury. Application to wounds or damaged skin is contraindicated due to the risk of exacerbating the condition. The use of heating pads or other heating devices is not recommended, as it may lead to adverse effects.

If symptoms persist for more than 3 days or worsen, discontinue use and consult a healthcare professional.

Warnings and Precautions

For external use only. It is imperative to avoid contact with the eyes and sensitive areas. In the event that the condition worsens or if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days, the patient should discontinue use and consult a healthcare professional.

If the condition persists for more than 3 days or worsens, it is also advised to stop use and seek medical advice.

Additionally, this product should be kept out of reach of children to prevent accidental ingestion or misuse.

Side Effects

Patients should be aware that the product is for external use only. It is important to avoid contact with the eyes and sensitive areas. If the condition worsens or if symptoms persist for more than 7 days, patients are advised to stop use and consult a doctor.

In the context of over-the-counter (OTC) use, patients should also stop use and seek medical advice if the condition persists for more than 3 days or worsens. Additionally, it is crucial to keep the product out of reach of children to prevent accidental ingestion or misuse.

Drug Interactions

There are no specific drug interactions identified for this medication. Additionally, no laboratory test interactions have been reported. 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 Natural Relief 1222 (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients should be kept out of reach of children to prevent accidental ingestion. For children aged 12 years and older, the recommended application is to apply liberally to the affected area. In the event of accidental swallowing, it is crucial to seek medical help or contact a poison control center immediately.

Geriatric Use

There is no specific information available 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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

The product has not been evaluated for use during pregnancy. Currently, there are no specific safety concerns or contraindications associated with the use of this product in pregnant patients. Additionally, no dosage modifications are recommended for individuals who are pregnant. There are also no special precautions indicated regarding the use of this product during pregnancy. Healthcare professionals should consider the lack of data when prescribing this product to pregnant patients and weigh the potential benefits against any unknown risks.

Lactation

The safety of this product during lactation has not been established. Caution should be exercised when using this product in nursing mothers. There is a potential for excretion in breast milk. It is recommended that lactating mothers consult a healthcare provider before using this product while breastfeeding.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

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 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, the use of activated charcoal may be considered if the patient presents within a suitable timeframe and if the ingestion of the substance is confirmed.

For specific management protocols, healthcare professionals should refer to established guidelines and consult poison control centers as necessary. Continuous assessment and supportive care remain paramount in the management of any overdose situation.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion or misuse. Patients should be instructed to stop using the product and consult a doctor if their condition persists for more than three days or worsens, as this may indicate a need for further medical evaluation.

When using this product, it is important for patients to avoid bandaging tightly, as this could lead to complications. They should also be cautioned against contact with the eyes, as this may cause irritation or injury. Additionally, patients should not apply the product to wounds or damaged skin to prevent adverse reactions. Finally, healthcare providers should inform patients to refrain from using heating pads or other heating devices in conjunction with this product, as this may exacerbate side effects or lead to further complications.

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 at a temperature range of 68 °F to 77 °F to maintain its efficacy and stability. Proper storage conditions should be observed to ensure the integrity of the product throughout its shelf life.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Natural Relief 1222, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)