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Bluedot Corn 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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2024
Label revision date
September 9, 2024
Drug Information (PDF)
Prescribing information, PDF file
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
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2024
Label revision date
September 9, 2024
Manufacturer
CREST MEDICAL LIMITED
Registration number
M030
NDC root
84713-102
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

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

Drug Overview

CRemover-1 is a medication designed specifically for the removal of corns and calluses, which are thickened areas of skin that can cause discomfort. By using CRemover-1, you can relieve pain associated with these skin conditions as it works to effectively remove the corns and calluses.

The product comes with an adhesive bandage that helps keep the medicated pad securely in place, ensuring that the treatment is applied correctly and remains effective. If you're dealing with corns or calluses, CRemover-1 may provide the relief you need.

Uses

If you're dealing with corns and calluses, this treatment can help you by effectively removing them. Not only does it assist in getting rid of these skin issues, but it also provides relief from the pain they can cause.

The product comes with an adhesive bandage that keeps the medicated pad securely in place, ensuring that the treatment works as intended. This way, you can go about your day while the medication does its job.

Dosage and Administration

To start treating your corn, first wash the affected area with soap and water, then dry it thoroughly. After 48 hours, you can apply a medicated bandage specifically designed for corn removal. Once you’ve applied the bandage, remember to remove it after the same 48-hour period.

You can repeat this process every 48 hours as needed, but do not continue for more than 14 days. If you find it helpful, you may soak the corn in warm water for about 5 minutes before applying the bandage, as this can assist in the removal process. Keep following these steps until the corn is completely gone.

What to Avoid

It's important to be aware of specific instructions regarding the use of this medication. If you accidentally swallow it, you should seek medical help immediately or contact a Poison Control Center. This is crucial for your safety, as prompt action can help address any potential issues.

Currently, there are no listed contraindications, risks of abuse or misuse, or concerns about dependence associated with this medication. Always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

This product is intended for external use only. You should not use it if you have diabetes, poor blood circulation, or if your skin is irritated, infected, or reddened. If you experience discomfort that lasts, it’s important to 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 are applying it to irritated, infected, or reddened skin.

If you experience discomfort that lasts, it’s important to stop using the product and consult your doctor. Additionally, keep this product out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, acting quickly can make a significant difference in the outcome.

Pregnancy Use

When it comes to using BLUEDOT Corn Removers, which contain salicylic acid, there is no specific information available about their safety or use during pregnancy. This means that the drug insert does not provide guidance on whether you should modify the dosage or take special precautions while pregnant.

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 weigh the potential risks and benefits based on your individual situation.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that salicylic acid, an ingredient in the product, may pass into your breast milk. Because of this, you should be cautious when using it, as there could be risks to your nursing infant. Always prioritize your baby's safety and seek guidance from a medical expert.

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 considering this medication, it’s important to consult with a healthcare provider. 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 the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver function and how it relates to your treatment. They can help ensure that your medication is safe and effective for you.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always feel free to ask questions and share your complete list of medications and any tests you may undergo. Your healthcare provider can help you understand how to manage your health effectively.

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, meaning you will place it directly on the skin. After 48 hours, you should remove the medicated bandage and repeat the application every 48 hours as needed, up to a maximum of 14 days, or until the corn is completely removed. Make sure to follow these instructions carefully for the best results.

FAQ

What is CRemover-1 used for?

CRemover-1 is used for the removal of corns and calluses.

How does CRemover-1 relieve pain?

It relieves pain by removing corns and calluses.

How should I apply CRemover-1?

Wash the affected area and dry it thoroughly, then apply the medicated bandage after 48 hours and remove it. Repeat every 48 hours as needed for up to 14 days.

Can I soak the corn before using CRemover-1?

Yes, you may soak the corn in warm water for 5 minutes to assist in removal.

Are there any contraindications for using CRemover-1?

There are no specific contraindications listed for CRemover-1.

What should I do if I swallow CRemover-1?

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

Who should not use CRemover-1?

Do not use CRemover-1 if you are diabetic, have poor blood circulation, or if the skin is irritated, infected, or reddened.

What should I do if discomfort lasts after using CRemover-1?

Stop use and ask a doctor if discomfort lasts.

Is CRemover-1 safe for nursing mothers?

Nursing mothers should consult a healthcare professional before using CRemover-1 due to the potential for salicylic acid to be excreted in breast milk.

What is the storage requirement for CRemover-1?

Store CRemover-1 between 0° to 40°C (32° to 104°F).

Packaging Info

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

Packaging configurations for Bluedot Corn Removers.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

CRemover-1 is a pharmaceutical compound identified by its unique chemical properties. The specific molecular weight and chemical formula are proprietary and not disclosed. It is formulated as a dosage form suitable for its intended therapeutic application. The appearance of CRemover-1 is consistent with standard pharmaceutical practices, ensuring quality and efficacy in its use. Inactive ingredients are included to support the stability and delivery of the active compound, although specific details regarding these components are not provided.

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 are advised to follow the outlined procedure for the application and administration of the treatment.

The affected area should be washed and dried thoroughly prior to application. After an initial period of 48 hours, a medicated bandage should be applied. Following this, the medicated bandage must be removed after 48 hours. This procedure may be repeated every 48 hours as necessary, for a maximum duration of 14 days, or until the corn is completely removed.

To facilitate the removal of the corn, it is recommended to soak the corn in warm water for 5 minutes prior to the application of the medicated bandage. This may enhance the effectiveness of the treatment.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that if the product is swallowed, immediate medical assistance should be sought or contact with a Poison Control Center should be made.

Warnings and Precautions

For external use only. This 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 the product is intended for external use only. It is contraindicated for individuals with diabetes or poor blood circulation, and it 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.

Additionally, if the product is ingested, immediate medical assistance should be sought, or the patient should contact a Poison Control Center without delay.

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

Packaging configurations for Bluedot Corn 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

There is no specific information regarding the use of BLUEDOT Corn Removers (salicylic acid patch) during pregnancy. The drug insert does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when recommending this product to women of childbearing potential. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Further studies may be necessary to establish the safety profile of salicylic acid patches in pregnant patients.

Lactation

Lactating mothers should consult a healthcare professional before using this product. There is a potential for excretion of salicylic acid in breast milk. Caution is advised when using this product while breastfeeding due to the potential risk to the infant.

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 prescribing information.

Overdosage

In the event of an overdosage, immediate medical assistance is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical help or contact a Poison Control Center without delay.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is recommended to determine the appropriate course of action.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. It is imperative that healthcare providers remain vigilant and prepared to address any complications that may arise from an overdosage scenario.

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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of 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 storage conditions must be adhered to, ensuring that the product is kept in a suitable container that protects it from environmental factors. Special handling requirements should 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 corn is removed.

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

Drug Information (PDF)

This file contains official product information for Bluedot Corn 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 Corn 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.

Learn more in our Editorial Policy

Last AI update:

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.