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Bluedot Callus Removers

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This product has been discontinued

Active ingredient
Salicylic Acid 40 g/100 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
September 9, 2024
Active ingredient
Salicylic Acid 40 g/100 g
Other brand names
Dosage form
Patch
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
September 9, 2024
Manufacturer
CREST MEDICAL LIMITED
Registration number
M030
NDC root
84713-103

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If you are a consumer or patient please visit this version.

Drug Overview

This medication is designed to help you remove corns and calluses, which are thickened areas of skin that can cause discomfort. By using this product, you can relieve pain associated with these skin issues, making it easier for you to walk and move comfortably. The medicated pad is held in place by an adhesive bandage, ensuring that it stays where it needs to be for effective treatment.

Uses

If you're dealing with corns and calluses, this treatment can help you by effectively removing them. Not only does it target these tough skin areas, but it also provides relief from the pain they can cause.

The medicated pad is designed to stay in place thanks to an adhesive bandage, ensuring that the treatment works effectively while you go about your day. With consistent use, you can expect to see improvements in the condition of your skin and a reduction in discomfort.

Dosage and Administration

To start treating your callus, first wash the affected area with soap and water, then dry it thoroughly. After 48 hours, you can apply a medicated bandage to the area. Once the bandage has been on for 48 hours, remove it and repeat the process as needed. You can continue this every 48 hours for up to 14 days, or until the callus is completely removed.

For better results, you may soak the callus in warm water for about 5 minutes before applying the bandage. This can help soften the callus, making it easier to treat. Remember to follow these steps consistently for the best outcome!

What to Avoid

You can feel confident using this medication, as there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with it. This means that, based on the available information, there are no known reasons that would prevent you from taking this medication safely. Always remember to follow your healthcare provider's guidance and reach out if you have any questions or concerns about your treatment.

Side Effects

You should only use this product externally. It is important not to use it if you have diabetes, poor blood circulation, or if your skin is irritated, infected, or reddened. If you experience discomfort that lasts, please stop using the product and consult a doctor.

In case of accidental swallowing, seek medical help immediately or contact a Poison Control Center. Always prioritize your safety and well-being when using any medication.

Warnings and Precautions

This product is intended for external use only. You should not use it if you have diabetes, poor blood circulation, or if you have irritated, infected, or reddened skin. It's important to keep this product out of reach of children. If a child swallows it, seek medical help or contact a Poison Control Center immediately.

If you experience discomfort that lasts, stop using the product and consult your doctor for further advice. Always prioritize your health and safety when using any medication or treatment.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to act quickly. You should seek medical help immediately or contact a Poison Control Center. They can provide guidance on what to do next.

Signs of an overdose can vary, but it’s crucial to be aware of any unusual symptoms. If you notice anything concerning, don’t hesitate to reach out for help. Remember, getting prompt assistance can make a significant difference in managing the situation effectively.

Pregnancy Use

When it comes to using this medication during pregnancy, there is no specific information available about its safety, dosage adjustments, or any special precautions you should take. This means that if you are pregnant or planning to become pregnant, it’s important to consult with your healthcare provider before using this product. They can help you understand any potential risks and make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding any medications you may be considering during this time.

Lactation Use

If you are breastfeeding and considering using BLUEDOT CALLUS REMOVERS, it's important to note that the drug insert does not provide specific information about nursing mothers or any potential effects on lactation (the process of producing breast milk). Since there are no guidelines or warnings mentioned, it may be wise to consult with your healthcare provider before using this product to ensure it is safe for you and your baby. Always prioritize your health and your infant's well-being when making decisions about medications or treatments while breastfeeding.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If your child swallows any of it, seek medical help immediately or contact a Poison Control Center for guidance. Taking these precautions can help ensure your child's safety.

Geriatric Use

When it comes to using this medication in older adults, there is no specific information available about dosage adjustments, safety concerns, or special precautions. This means that if you or a loved one is an older adult, it’s important to consult with a healthcare provider before starting the medication. They can help determine the best approach based on individual health needs and any other medications being taken. Always prioritize open communication with your healthcare team to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

Hepatic Impairment

If you have liver problems, it's important to know that there are no specific guidelines or dosage adjustments mentioned for your condition in the available information. This means that the standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may want to conduct regular liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that this medication is generally considered safe to use alongside other treatments and tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you.

Always remember that discussing your full list of medications and any lab tests with your healthcare provider is crucial. This way, you can avoid any potential issues and receive the best care tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 0° to 40°C (32° to 104°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a sterile field (a clean area free from germs) to prevent contamination. Always follow any specific disposal instructions provided to ensure safe and responsible disposal of any components.

Additional Information

You will apply this medication topically, using a medicated bandage. After 48 hours, remove the bandage and repeat the application every 48 hours as needed, up to a maximum of 14 days, or until the callus is completely removed. Make sure to follow these instructions carefully for the best results.

FAQ

What is the purpose of this drug?

This drug is used for the removal of corns and calluses, relieving pain by removing these skin growths.

How should I apply the medicated bandage?

First, wash the affected area and dry it thoroughly. Then, apply the medicated bandage after 48 hours and remove it afterward.

How often can I repeat the procedure?

You can repeat the procedure every 48 hours as needed for up to 14 days, or until the callus is removed.

Are there any warnings I should be aware of?

Yes, this product is for external use only. Do not use it if you are diabetic, have poor blood circulation, or on irritated or infected skin.

What should I do if discomfort lasts?

If discomfort lasts, you should stop using the product and ask a doctor for advice.

What should I do if the product is swallowed?

If swallowed, get medical help or contact a Poison Control Center immediately.

Is there any specific information regarding use during pregnancy?

The drug insert does not provide specific information regarding the use of this product during pregnancy.

What is the storage requirement for this drug?

Store the drug between 0° to 40°C (32° to 104°F).

Packaging Info

Below are the non-prescription pack sizes of Bluedot Callus Removers (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bluedot Callus Removers.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

CallusRmvr-1 is identified by the SPL code 34089-3. It is a pharmaceutical product formulated for the removal of calluses. The specific characteristics, including its molecular weight and chemical formula, are not provided in the extracted data. Further details regarding its dosage form and appearance are also not included.

Uses and Indications

This drug is indicated for the removal of corns and calluses. It provides relief from pain associated with these conditions by effectively removing the corns and calluses. The formulation includes an adhesive bandage that secures the medicated pad in position, ensuring optimal contact with the affected area for enhanced efficacy.

Dosage and Administration

Healthcare professionals should instruct patients to wash the affected area thoroughly and ensure it is completely dry before application. Following this, a medicated bandage should be applied. After 48 hours, the medicated bandage must be removed.

This procedure may be repeated every 48 hours as necessary, for a maximum duration of 14 days, or until the callus is effectively removed. To facilitate the removal of the callus, soaking the affected area in warm water for 5 minutes prior to the application of the medicated bandage is recommended.

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

For external use only. The product is contraindicated in individuals with diabetes or those who exhibit poor blood circulation. It should not be applied to irritated skin or any area that is infected or reddened.

Healthcare professionals should advise patients to discontinue use and seek medical advice if discomfort persists. It is essential to keep this 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.

Side Effects

Patients should be aware that this product is for external use only. It is contraindicated for individuals who are diabetic or have poor blood circulation. Additionally, the product should not be applied to irritated skin or any area that is infected or reddened.

In the event that discomfort persists after application, patients are advised to discontinue use and consult a healthcare professional.

Furthermore, if the product is ingested, it is imperative to seek medical assistance or contact a Poison Control Center immediately.

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 Bluedot Callus Removers (salicylic acid). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Bluedot Callus Removers.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication 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

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

The available prescribing information does not provide specific data regarding the use of this product during pregnancy. Consequently, the safety concerns, dosage modifications, or special precautions for pregnant patients remain undefined. Healthcare professionals are advised to consider the lack of information when prescribing this medication to women of childbearing potential and to weigh the potential risks versus benefits in the context of individual patient circumstances. Further research may be necessary to elucidate the implications of this product on fetal outcomes.

Lactation

There is no specific information regarding the use of BLUEDOT CALLUS REMOVERS (salicylic acid patch) in lactating mothers or lactation considerations. The effects on breastfed infants and the excretion of salicylic acid in breast milk have not been established. Therefore, healthcare professionals should exercise caution when recommending this product to lactating mothers.

Renal Impairment

Patients with renal impairment may not have specific dosage adjustments, special monitoring, or safety considerations outlined in the prescribing information. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment and monitoring of these patients.

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, immediate medical intervention is crucial. If the substance is ingested, it is imperative to seek medical assistance or contact a Poison Control Center without delay.

Healthcare professionals should be aware that prompt action can significantly influence the outcome of an overdosage situation. Symptoms may vary depending on the specific substance involved, and monitoring for any adverse effects is essential.

Management of overdosage typically involves supportive care and symptomatic treatment. It is recommended that healthcare providers assess the patient's condition thoroughly and initiate appropriate interventions based on the clinical presentation.

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 provided in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of the reach of children to prevent accidental ingestion. It is important to emphasize that if the medication is swallowed, patients should seek medical help or contact a Poison Control Center immediately. This guidance is crucial for ensuring patient safety and minimizing potential risks associated with accidental exposure.

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 a temperature range of 0° to 40°C (32° to 104°F) to maintain its efficacy and safety. Proper container requirements should be adhered to, ensuring that the product is kept in an appropriate environment. Special handling needs must be observed to prevent any compromise to the product's integrity.

Additional Clinical Information

The medication is administered topically, with a specific application protocol. Clinicians should instruct patients to apply a medicated bandage after 48 hours and to remove it thereafter. This procedure may be repeated every 48 hours as necessary, up to a maximum of 14 days, or until the callus is fully removed.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

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

View product document (PDF)

Data Generation & Sources

This page was automatically generated and is maintained by the AllDrugs AI Data-Science Team. It was built from the FDA Structured Product Label (DailyMed) for Bluedot Callus Removers, retrieved by a validated AI data-extraction workflow.

All FDA-listed dosage forms and strengths are shown in the Packaging & NDC Codes section above. Regulatory status appears in the Summary Information panel above and was verified in the FDA National Drug Code directory and the NSDE NDC Directory daily file.

Note: an automated daemon monitors NSDE checksums; when the record for this NDC changes, the new file is pulled instantly and this page is refreshed.

No human clinician has reviewed this version.

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Primary FDA sources:

Orange Book data shown on this page are limited to Regulatory Status (Rx), Established Pharmacologic Class (EPC), and Mechanism of Action (MoA).

Regulatory data notice: Information on this page is reproduced verbatim from FDA public databases (NSDE, Orange Book, Purple Book, DailyMed SPL). NDA/ANDA drugs are FDA-approved, BLA biologics are FDA-licensed. Inclusion alone does not guarantee current market availability or imply FDA endorsement.

Medical disclaimer: This AI-generated content is provided for educational purposes only and does not constitute medical advice. Always consult a licensed healthcare professional for diagnosis or treatment decisions.