Maximum Strength Medicated Foot Powder

Description

Maximum Strength Medicated Foot Powder is formulated to provide effective relief for foot-related conditions. This powder is designed for topical application and is intended to alleviate discomfort associated with excessive moisture and odor. The product is characterized by its fine, powdery texture, which facilitates easy application and adherence to the skin.

Uses and Indications

This drug is indicated for the temporary relief of pain and itching associated with minor cuts, scrapes, sunburn, insect bites, prickly heat, rashes, minor burns, and minor skin irritation. Additionally, it is effective in drying the oozing of poison ivy, oak, and sumac.

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

Dosage and Administration

Adults and children aged 2 years and older are instructed to apply the medication freely up to 3 or 4 times daily. For children under 2 years of age, it is recommended to consult a physician prior to use.

For optimal results, it is essential to ensure that the skin is thoroughly dried before application.

Contraindications

Use of this product is contraindicated in patients with a known hypersensitivity to any of its components.

Additionally, the product should not be applied to the eyes or used in the genital area due to the potential for irritation and adverse effects.

Warnings and Precautions

External use only is mandated for this product. It is imperative to avoid contact with the eyes and to refrain from applying it to the genital area.

Healthcare professionals should advise patients to discontinue use and seek medical consultation if any of the following occur: worsening of conditions, persistence or increase in redness, irritation, swelling, or pain, or if symptoms do not improve within 7 days. Additionally, if symptoms resolve and then recur within a few days, medical advice should be sought.

In the event of accidental ingestion, immediate medical assistance is crucial. Patients should be instructed to contact a Poison Control Center at 1-800-222-1222 or seek emergency medical help without delay.

Side Effects

Patients using this product should be aware that it is for external use only and should avoid contact with the eyes. It is not intended for use in the genital area.

In clinical practice, patients are advised to stop using the product and consult a healthcare professional if any of the following occur: worsening of conditions, persistence or increase of redness, irritation, swelling, or pain, or if symptoms do not improve within 7 days. Additionally, if symptoms clear up and then recur within a few days, medical consultation is recommended.

This product should be kept out of reach of children. In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center immediately at 1-800-222-1222.

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 Maximum Strength Medicated Foot Powder (medicated foot powder). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients under 2 years of age should consult a physician prior to use. For children aged 2 years and older, the product may be applied freely up to 3 or 4 times daily.

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 potential adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

There is no information available regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or any special precautions that should be taken. Healthcare professionals are advised to consider the lack of data when prescribing this medication to pregnant patients and to weigh the potential risks and benefits. Women of childbearing potential should be counseled accordingly.

Lactation

There are no specific warnings or precautions regarding the use of this medication in nursing mothers. Additionally, there are no specific considerations or information related to lactation provided in the available data. Therefore, healthcare professionals may consider the absence of contraindications when advising lactating mothers.

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 clinical trials for this medication. Consequently, there is no available information regarding 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 warranted based on clinical judgment.

Overdosage

In the event of accidental ingestion, it is imperative to seek immediate medical assistance or contact a Poison Control Center at 1-800-222-1222. Prompt action is crucial to ensure the safety and well-being of the patient.

Healthcare professionals should be aware that symptoms of overdosage may vary depending on the substance involved. Therefore, a thorough assessment of the patient's condition is essential.

Management of overdosage should be guided by the clinical presentation and may include supportive care and symptomatic treatment. Continuous monitoring of the patient's vital signs and overall status is recommended to address any complications that may arise.

In all cases of suspected overdosage, it is vital to gather as much information as possible regarding the substance, the amount ingested, and the time of ingestion to facilitate appropriate medical intervention.

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 these contexts.

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. In the event of accidental ingestion, patients should seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

Patients should be instructed to avoid contact with the eyes while using this product and to refrain from applying it to the genital area. They should be informed to stop using the product and consult a doctor if their condition worsens or if they experience persistent or increasing redness, irritation, swelling, or pain.

Additionally, patients should be counseled to seek medical advice if their symptoms do not improve within 7 days, or if symptoms clear up and then recur within a few days. This guidance is essential for ensuring patient safety and effective use of the product.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored in a cool, dry place, away from excessive heat. Freezing is not permitted, as it may compromise the product's quality. After opening, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The product is administered topically, with a recommended application frequency of up to three or four times daily for adults and children aged 2 years and older. For children under 2 years, consultation with a physician is advised prior to use.

Clinicians should counsel patients that the product is for external use only and must be kept away from the eyes and genital area. Patients are instructed to discontinue use and seek medical advice if symptoms worsen, or if redness, irritation, swelling, or pain persists or increases. If symptoms do not improve within 7 days or recur shortly after resolution, medical consultation is also recommended. Additionally, the product should be kept out of reach of children, and in the event of accidental ingestion, immediate medical assistance or contact with a Poison Control Center (1-800-222-1222) is necessary.

Drug Information (PDF)

This file contains official product information for Maximum Strength Medicated Foot Powder, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)