Walgreens Corn Remover

Description

Salicylic Acid 40% is a topical formulation designed for the effective removal of corns. The product is presented in the form of a medicated pad that adheres securely to the skin, ensuring it remains in place during use. This formulation is water-resistant, allowing for continued efficacy even in moist conditions. Salicylic Acid serves as the active ingredient, comparable to that found in Dr. Scholl's® OneStep Corn Removers, and is capable of achieving corn removal in as few as two treatments.

Uses and Indications

This drug is indicated for the removal of corns. It provides relief from pain associated with corns through its effective removal properties.

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

Dosage and Administration

The affected area should be washed thoroughly. If desired, the area may be soaked in warm water for 5 minutes to facilitate cleansing. After washing, the area must be dried completely.

The medicated bandage should be removed from its backing and applied directly over the corn, ensuring that the medicated area is in direct contact with the affected skin.

The medicated bandage should remain in place for 48 hours. After this period, the bandage must be removed.

This procedure may be repeated every 48 hours as necessary, continuing until the corn is removed, for a maximum duration of 14 days.

Contraindications

Use of this product is contraindicated in the following situations:

Patients with diabetes should not use this product due to potential complications associated with glycemic control.

Application on irritated, broken, or infected skin is contraindicated to prevent exacerbation of the condition and to avoid further irritation or infection.

Individuals with poor blood circulation should refrain from using this product, as it may impair healing and exacerbate existing vascular issues.

Warnings and Precautions

For external use only. This product should be utilized strictly as directed to ensure safety and efficacy.

Contraindications This product must not be used in the following circumstances:

• In individuals with diabetes.

• On skin that is irritated, broken, or infected.

• In patients with poor blood circulation.

Monitoring and Consultation If discomfort persists after application, it is imperative to seek medical advice from a healthcare professional, such as a doctor or podiatrist.

Safety Precautions It is essential to keep this product out of the reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control center without delay.

Side Effects

Patients should be aware that the product is for external use only and should be used strictly as directed. It is contraindicated for individuals who are diabetic, have poor blood circulation, or have irritated, broken, or infected skin.

In clinical practice, if discomfort persists after application, patients are advised to consult their doctor or podiatrist for further evaluation. Additionally, it is crucial 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 with a Poison Control center is recommended.

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 Walgreens Corn Remover (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Pediatric Use

Pediatric patients should be advised to keep this medication 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.

Geriatric Use

Elderly patients may not have specific information regarding the use of this medication, including dosage adjustments, safety concerns, or special precautions. As such, 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 therapeutic response, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should be aware that the safety of this medication during pregnancy has not been established. There are no available data regarding the potential risks or fetal outcomes associated with the use of this medication in pregnant individuals. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to discuss the potential risks and benefits with their patients. It is recommended that healthcare providers remain vigilant and informed about any emerging data related to the use of this medication in pregnant patients.

Lactation

No information related to nursing mothers or lactation is provided in the drug insert for Walgreens Corn Remover. Therefore, the effects on breastfed infants and the excretion of the drug in breast milk are unknown. Healthcare professionals should exercise caution when considering the use of this product in 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 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 event of an overdosage, it is imperative to seek immediate medical assistance. Healthcare professionals should advise patients or caregivers to contact a Poison Control center without delay if the substance has been ingested.

Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment of the patient's condition is essential. Prompt recognition of symptoms can facilitate timely intervention and management.

Management of overdosage should be guided by the severity of symptoms and the specific circumstances surrounding the incident. Healthcare providers are encouraged to follow established protocols for the treatment of overdosage, which may include supportive care and symptomatic treatment as necessary.

In all cases, the priority is to ensure the safety and well-being of the patient through appropriate medical evaluation and 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 for SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is crucial to emphasize the importance of safety in the home environment, particularly for households with young children.

In the event that the medication is swallowed, patients should be instructed to seek medical help or contact a Poison Control center immediately. This prompt action is essential to ensure appropriate care and intervention if necessary.

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 within the temperature range of 59° to 86°F (15° to 30°C) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept in a suitable environment to prevent degradation.

Additional Clinical Information

The product is administered topically, with the procedure to be repeated every 48 hours as needed until the corn is removed, for a maximum duration of 14 days. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

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

View product document (PDF)