Wormwood Patch

Description

No specific description details are available for SPL code 34089-3.

Uses and Indications

This drug is indicated for the application of a plaster to the neck or other specified areas of the body. The plaster should be applied every 8 hours, following the removal of the backing paper from the adhesive side.

There are no teratogenic or nonteratogenic effects associated with this drug as per the available data.

Dosage and Administration

The plaster should be applied to the neck or other designated areas of the skin. Prior to application, the backing paper must be removed from the plaster. The plaster is to be administered every 8 hours. Care should be taken to ensure that the skin is clean and dry before application to promote optimal adhesion and effectiveness.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

Healthcare professionals are advised to exercise caution when administering this product to pregnant women and children. The safety profile in these populations has not been fully established, and careful consideration should be given to the potential risks versus benefits.

This product is contraindicated for use in patients with skin ulcers and those presenting with high fever. The application in these conditions may exacerbate the underlying issues and lead to further complications.

Additionally, the use of this product is strictly prohibited in individuals with known allergies. Healthcare providers should ensure that patients are screened for any history of allergic reactions prior to administration.

Special care should be taken to avoid application on sensitive skin, particularly in the vicinity of the eye area. The delicate nature of this skin can lead to adverse reactions, and healthcare professionals should instruct patients accordingly to prevent potential irritation or injury.

Side Effects

Patients should be aware of several important warnings associated with the use of this medication. It is advised that pregnant women and children use this product with caution due to potential risks. The medication is not suitable for individuals with skin ulcers or those experiencing high fever. Additionally, it is strictly forbidden to use this product for allergies. Care should also be taken to avoid application on sensitive skin, particularly in the area near the eyes.

These precautions are essential to ensure the safety and well-being of patients using this medication.

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 Wormwood Patch (menthol). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients should be advised to keep the medication out of reach to prevent accidental ingestion. Caution is advised when administering this medication to pregnant women and children, as safety and efficacy in these populations may not be fully established.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Pregnant women and children should use this medication with caution. The potential risks associated with the use of this drug during pregnancy have not been fully established. Healthcare professionals are advised to carefully consider the benefits and risks before prescribing this medication to pregnant patients. It is essential to monitor for any adverse effects and to counsel women of childbearing potential regarding the importance of effective contraception during treatment.

Lactation

Lactating mothers should use this medication with caution. There is limited data available regarding the excretion of this drug in human breast milk and its effects on breastfed infants. Healthcare professionals are advised to consider the potential risks and benefits when prescribing this medication to lactating mothers. Close monitoring of breastfed infants may be warranted to assess any potential adverse effects.

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 initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, the use of specific antidotes or treatments should be considered based on the substance involved and the clinical presentation. Consultation with a poison control center or a medical toxicologist may provide additional guidance on the management of overdose cases.

Documentation of the incident, including the substance, amount ingested, and time of ingestion, is crucial for effective management and treatment planning.

Nonclinical Toxicology

Pregnant women and children should use this product with caution due to potential teratogenic effects. It is not suitable for individuals with skin ulcers or high fever, and its use is contraindicated in patients with allergies. Additionally, the product should not be applied to sensitive skin near the eye area.

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 to ensure the safety of young individuals.

Storage and Handling

The product is supplied in a configuration that ensures optimal preservation of its integrity. It should be stored in a dry place, away from light, to maintain its efficacy. The shelf life of the product is 24 months from the date of manufacture. Proper storage conditions are essential to ensure the product remains effective throughout its intended use period.

Additional Clinical Information

Patients should apply the plaster to the neck or other areas by removing the backing paper and adhering it every 8 hours. Caution is advised for pregnant women and children, as the plaster is not suitable for individuals with skin ulcers or high fever. It is contraindicated for use in patients with allergies and should not be applied to sensitive skin, particularly near the eye area.

Drug Information (PDF)

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

View product document (PDF)