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Coralite Pain Relief

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Active ingredients
  • Camphor (synthetic) 1.2 g/100 g
  • Menthol 5.7 g/100 g
  • Methyl Salicylate 6.3 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 2016
Label revision date
October 21, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 1.2 g/100 g
  • Menthol 5.7 g/100 g
  • Methyl Salicylate 6.3 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 2016
Label revision date
October 21, 2025
Manufacturer
United Exchange Corp.
Registration number
M017
NDC root
65923-564
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

This medication is designed for use in adults and children aged 12 years and older. It is typically applied to specific areas of the skin that require treatment. The patch can be used up to 3 to 4 times a day, but it should not be worn for more than 4 hours at a time. If you have a child under 12, it's important to consult a doctor before use.

Uses

It seems that there are no specific uses or indications provided for this medication. This means that the information about what this drug is intended to treat or how it can be used is not available. If you have any questions or need further clarification about this medication, it's best to consult with a healthcare professional who can provide you with the most accurate and relevant information.

Dosage and Administration

It seems that there is no specific dosage or administration information available for the medication you are inquiring about. This means that details such as how much to take, how often to take it, or how to apply it are not provided.

If you have any questions about how to use this medication or need guidance on its administration, it's best to consult with your healthcare provider or pharmacist. They can give you the most accurate and personalized information based on your health needs.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should never apply it to wounds or damaged skin, and avoid using it with a heating pad. If you are allergic to any of the ingredients, do not use the product. Additionally, it is not suitable for children under 12 years of age who have arthritis-like conditions.

Make sure to follow these guidelines: do not use the product other than as directed, and keep it away from your eyes, mucous membranes, or any rashes. Avoid wrapping the area tightly, and stop using it at least one hour before taking a bath or shower. Lastly, do not apply it right after bathing or showering. Following these instructions will help ensure your safety and the effectiveness of the product.

Side Effects

If you are considering using this medication, it's important to be aware of potential side effects. You should consult a doctor if you have a history of allergic reactions to aspirin or salicylates, as this could increase your risk of an adverse reaction.

You should also stop using the medication and seek medical advice if you notice any redness, irritation, or rash developing, if your condition worsens, or if symptoms persist for more than 7 days. Additionally, if your symptoms improve but then return within a few days, it's advisable to consult a doctor.

Warnings and Precautions

This product is for external use only, so please avoid applying it to wounds or damaged skin. If you have a history of allergic reactions to aspirin or salicylates, it's important to consult your doctor before using this product. Additionally, do not use it with a heating pad or on children under 12 years of age who have arthritis-like conditions.

You should stop using this product and call your doctor if you notice any redness, irritation, or rash, if your condition worsens, or if symptoms persist for more than 7 days. If your symptoms improve and then return within a few days, reach out to your doctor as well. Keep this product out of reach of children, and if it is swallowed, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the potential risks associated with taking more than the recommended dose. If you suspect an overdose, look for signs such as unusual drowsiness, confusion, or difficulty breathing.

In the event of an overdose, you should seek immediate medical help. Contact your local emergency services or go to the nearest hospital. It's crucial to act quickly, as timely intervention can make a significant difference in your recovery. Always remember to keep medications out of reach and follow the prescribed dosage to ensure your safety.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using this medication. They can provide guidance on whether it’s safe for you and your baby. Always prioritize your health and the health of your child by seeking expert advice.

Lactation Use

If you are pregnant or breastfeeding, it’s important to consult with a healthcare professional before using any medication. This ensures that you understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

If your child is under 12 years old and has arthritis-like conditions, it's important not to use this medication. For any child under 12, you should consult a doctor before starting treatment. This ensures that the medication is safe and appropriate for their specific health needs. Always prioritize your child's well-being by seeking professional guidance.

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 be adjusted 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 condition. They can provide guidance based on your individual health needs.

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 if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place away from direct sunlight. Exposure to sunlight can damage the product, while excessive moisture can compromise its integrity.

When handling the product, be mindful of these storage conditions to maintain its effectiveness. Always check for any signs of damage or changes before use, and follow any specific disposal instructions provided to ensure safe and responsible handling.

Additional Information

You should apply this medication topically to the affected area no more than 3 to 4 times a day. Remember not to wear the patch for more than 4 hours at a time. If you are pregnant or breastfeeding, it's important to consult a health professional before using this product.

Keep the medication out of reach of children. If a child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

FAQ

Who can use this drug?

The drug is indicated for adults and children 12 years of age and over. For children under 12 years, consult a doctor.

What are the directions for using the patch?

Clean and dry the affected area, remove the patch from the film, and apply it not more than 3 to 4 times daily. Do not wear the patch for more than 4 hours.

Are there any contraindications for using this drug?

Do not use on wounds or damaged skin, with a heating pad, or if you are allergic to any ingredients. Also, do not use on a child under 12 years of age with arthritis-like conditions.

What should I do if I experience redness or irritation?

Stop use and ask a doctor if redness is present, irritation or rash develops, or if the condition worsens or symptoms persist for more than 7 days.

What precautions should I take if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before use.

What should I do if the patch is swallowed?

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Can I use this patch if I have a history of allergies?

If you are prone to allergic reactions from aspirin or salicylates, consult a doctor before use.

What should I avoid while using this patch?

Avoid contact with eyes, mucous membranes, or rashes, and do not bandage tightly. Discontinue use at least 1 hour before a bath or shower.

Packaging Info

Below are the non-prescription pack sizes of Coralite Pain Relief (camphor, menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Coralite Pain Relief.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No description information is available for the specified drug.

Uses and Indications

This drug is indicated for use in specific patient populations as determined by clinical guidelines. The precise indications and usage have not been detailed in the provided information.

Healthcare professionals are advised to consult relevant clinical resources and guidelines to determine appropriate applications of this drug in practice. Further information regarding teratogenic and nonteratogenic effects is not available in the current data set.

Dosage and Administration

No dosage and administration information is available for this product. Healthcare professionals are advised to consult the prescribing information or relevant clinical guidelines for specific dosing recommendations and administration techniques.

Contraindications

Use of this product is contraindicated in the following situations:

  • Application on wounds or damaged skin is prohibited due to the risk of exacerbating the condition.

  • Concurrent use with a heating pad is not recommended, as it may lead to increased irritation or adverse effects.

  • Individuals with known allergies to any ingredients in this product should avoid its use to prevent allergic reactions.

  • The product should not be used in children under 12 years of age with arthritis-like conditions, as safety and efficacy have not been established in this population.

  • The product should not be used other than as directed to ensure safety and effectiveness.

  • Contact with the eyes, mucous membranes, or rashes should be avoided to prevent irritation.

  • Tight bandaging is contraindicated to allow for proper circulation and prevent skin damage.

  • Discontinue use at least 1 hour prior to bathing or showering to minimize the risk of adverse reactions.

  • Avoid application immediately after bathing or showering to ensure skin integrity and product efficacy.

Warnings and Precautions

For external use only. Individuals with a known allergy to aspirin or salicylates should consult a healthcare professional prior to use to assess potential risks.

General precautions must be observed to ensure safe application. The product should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad. Additionally, it is contraindicated for use in children under 12 years of age who present with arthritis-like conditions. Users should also refrain from using the product if they are allergic to any of its ingredients.

Patients are advised to discontinue use and seek medical advice if any of the following occur: the presence of redness, irritation, or rash; worsening of the condition; or if symptoms persist beyond 7 days. Furthermore, if symptoms resolve and then recur within a few days, medical consultation is recommended.

It is imperative 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 advised.

Side Effects

Patients should be aware of the potential for adverse reactions associated with the use of this product. Individuals who are prone to allergic reactions from aspirin or salicylates are advised to consult a healthcare professional prior to use.

In clinical practice, it is recommended that patients discontinue use and seek medical advice if they experience any of the following: the presence of redness, the development of irritation or rash, worsening of the condition, or if symptoms persist for more than 7 days. Additionally, if symptoms resolve and then recur within a few days, patients should also stop use and consult a doctor.

Before using this product, patients should ask a healthcare provider if they have redness over the affected area, as this may indicate a need for further evaluation.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Coralite Pain Relief (camphor, menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Coralite Pain Relief.
Details

Pediatric Use

Pediatric patients with arthritis-like conditions should not be treated with this medication if they are under 12 years of age. For children in this age group, it is essential to consult a healthcare professional before use.

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

Pregnancy

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data regarding the excretion of this medication in human breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating individuals.

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 overdosage information, it is essential for healthcare professionals to remain vigilant and prepared for potential scenarios involving overdose.

Healthcare providers should be aware that the clinical presentation of an overdose may vary significantly depending on the substance involved and the individual patient’s characteristics. Symptoms of overdose can range from mild to severe and may include altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of suspected overdosage, immediate medical evaluation is recommended. Healthcare professionals should assess the patient's vital signs and conduct a thorough clinical examination. Supportive care should be initiated as necessary, which may include airway management, intravenous fluids, and monitoring of vital parameters.

If specific antidotes or treatments are available for the substance involved, they should be administered according to established protocols. Consultation with a poison control center or toxicology expert may also be beneficial in managing the case effectively.

It is crucial to document all findings and interventions thoroughly, as this information may be vital for ongoing patient management and for reporting purposes.

Nonclinical Toxicology

If pregnant or breastfeeding, it is advised to consult a health professional prior to use. No non-teratogenic effects have been provided in the insert. Additionally, there is no information available regarding nonclinical toxicology or animal pharmacology and toxicology in the insert.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children. It is important to emphasize that if the medication is swallowed, patients should seek medical help immediately or contact a Poison Control Center without delay. This precaution is crucial to ensure the safety and well-being of children who may inadvertently access the medication.

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 in a cool, dry place, avoiding direct sunlight to maintain its integrity. Additionally, the product should be protected from excessive moisture to ensure optimal quality and efficacy. Proper handling and storage conditions are crucial for preserving the product's effectiveness.

Additional Clinical Information

The medication is administered topically, with a recommended application to the affected area not exceeding 3 to 4 times daily. Patients should not wear the patch for more than 4 hours at a time.

Clinicians should advise patients who are pregnant or breastfeeding to consult a health professional prior to use. It is also important to keep the medication out of reach of children; if ingested, immediate medical assistance or contact with a Poison Control Center is necessary.

Drug Information (PDF)

This file contains official product information for Coralite Pain Relief, 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 Coralite Pain Relief, 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.