ADD CONDITION

items per page

Coralite Pain Relief Stick

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredients
  • Menthol 4 g/100 g
  • Methyl Salicylate 1 g/100 g
Other brand names
Dosage form
Stick
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2016
Label revision date
February 10, 2016
Active ingredients
  • Menthol 4 g/100 g
  • Methyl Salicylate 1 g/100 g
Other brand names
Dosage form
Stick
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2016
Label revision date
February 10, 2016
Manufacturer
United Exchange Corp.
Registration number
part348
NDC root
65923-120

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

It seems that the provided information does not include specific details about the drug's name, general description, or its mechanism of action. Therefore, I am unable to create a summary that addresses what the drug is or what it is used for. If you have more information or specific details about the drug, please share them, and I would be happy to help you craft a consumer-friendly summary.

Uses

You can use this product to help with specific skin issues by applying it generously to the affected area. Make sure to massage it into your skin until it is fully absorbed. You can repeat this process as needed, but do not apply it more than four times a day.

If you are considering using this product for a child under 10 years old, it's important to consult a doctor first to ensure it's safe for them. Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) associated with this product.

Dosage and Administration

It seems that there are no specific dosage or administration details available for this medication. This means that you should consult your healthcare provider for personalized instructions on how to take or use it. They will provide you with the necessary information regarding the correct amount, how to administer it, and how often you should do so. Always follow their guidance to ensure safe and effective use of the medication.

What to Avoid

It's important to use this medication safely to avoid any potential issues. You should not bandage the area tightly or use a heating pad while using this product. Additionally, make sure to avoid contact with your eyes and mucous membranes, as well as applying it to any wounds or damaged skin.

By following these guidelines, you can help ensure that you use the medication effectively and safely. If you have any questions or concerns, don't hesitate to reach out to your healthcare provider for more information.

Side Effects

If you are allergic to salicylates, such as aspirin, it’s important to consult your doctor before using this medication. Be aware of potential adverse reactions; if your condition worsens, symptoms last longer than 7 days, or if they improve and then return shortly after, you should stop using the medication and seek medical advice. Additionally, if you notice any redness or irritation, it’s best to contact your healthcare provider.

Warnings and Precautions

This product is for external use only. If you are pregnant or breastfeeding, please consult a healthcare professional before using it. Additionally, if you have an allergy to salicylates (which includes aspirin), do not use this product without first talking to your doctor.

If you accidentally swallow the product, seek medical help immediately or contact a Poison Control Center. You should also stop using the product and call your doctor if your condition worsens, if symptoms last longer than 7 days, if they improve and then come back within a few days, or if you notice any redness or irritation.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and 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 you have a child under 10 years old, it's important to consult a doctor before using this medication. This ensures that the treatment is safe and appropriate for their age and health needs. Always prioritize professional guidance when it comes to your child's health.

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 should be used if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help determine the best course of action based on your individual situation.

Drug Interactions

It's important to be cautious when taking any medication, especially if you have allergies. If you are allergic to salicylates, which include aspirin, you should consult your healthcare provider before using this medication. They can help determine if it's safe for you.

Additionally, while there are no specific interactions with other drugs or laboratory tests noted, it's always a good practice to discuss all medications and tests with your healthcare provider. This ensures that you receive the best care and minimizes any potential risks.

Storage and Handling

To ensure the best performance of your product, store it at a temperature between 20° to 25°C (68° to 77°F). This temperature range helps maintain the integrity and effectiveness of the device.

When handling the product, always do so with clean hands and in a clean environment to avoid contamination. If you have any specific disposal instructions, please follow them carefully to ensure safety and compliance.

Additional Information

You should apply this medication topically to the affected area. For adults and children aged 10 years and older, apply it generously and massage it into the skin until fully absorbed. You can repeat this process as needed, but do not exceed four applications in a day. If the patient is under 10 years old, it's important to consult a doctor before use.

FAQ

How should I use this medication?

Apply generously to the affected area and massage it into the skin until thoroughly absorbed. You can repeat this process as necessary, but do not exceed 4 times daily.

What should I do if I am using this medication on a child under 10 years old?

Consult a doctor before using this medication on children under 10 years of age.

Are there any specific warnings I should be aware of?

This medication is for external use only. Avoid contact with eyes and mucous membranes, and do not apply it to wounds or damaged skin.

What should I do if I experience worsening symptoms?

Stop using the medication and consult a doctor if your condition worsens, symptoms persist for more than 7 days, or if redness or irritation develops.

Is there an allergy alert for this medication?

Yes, do not use this medication if you are allergic to salicylates, including aspirin, without consulting a physician.

What should I do if I accidentally swallow this medication?

Get medical help or contact a Poison Control Center immediately if swallowed.

Can I use this medication if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, consult a health professional before using this medication.

What is the recommended storage condition for this medication?

Store the medication at 20° to 25°C (68° to 77°F).

Packaging Info

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

Packaging configurations for Coralite Pain Relief Stick.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

No relevant information is available for SPL code 34089-3.

Uses and Indications

This drug is indicated for topical application to affected areas of the skin. It should be applied generously and massaged into the skin until thoroughly absorbed. The application may be repeated as necessary, but should not exceed four times daily.

For pediatric patients, specifically those under 10 years of age, it is recommended to consult a healthcare professional prior to use.

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

Dosage and Administration

There is currently no specific dosage or administration information available for this medication. Healthcare professionals are advised to refer to the prescribing information or clinical guidelines for detailed instructions regarding the appropriate dosage, route, method, and frequency of administration. It is essential to consider individual patient factors and clinical judgment when determining the appropriate treatment regimen.

Contraindications

The product should not be used in the following situations:

Tight bandaging or the use of a heating pad is contraindicated, as this may lead to adverse effects. Contact with eyes and mucous membranes must be avoided to prevent irritation or injury. Additionally, application to wounds or damaged skin is contraindicated due to the risk of exacerbating the condition or causing further harm.

Warnings and Precautions

For external use only. It is imperative that healthcare professionals advise patients who are pregnant or breastfeeding to consult a health professional prior to use.

An allergy alert is warranted; patients should be cautioned against using this product if they have a known allergy to salicylates, including aspirin, without prior consultation with a physician.

In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted without delay.

Patients should be instructed to discontinue use and consult a healthcare provider if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. Additionally, if redness or irritation develops, it is essential to seek medical advice promptly.

Side Effects

Patients should be aware of the potential for serious allergic reactions, particularly those who have a known allergy to salicylates, including aspirin. It is advised that individuals consult a physician before using the product if they have such allergies.

In addition to the allergy alert, patients are instructed to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. The presence of redness or the development of irritation also warrants immediate consultation with a healthcare professional.

Drug Interactions

Patients with a known allergy to salicylates, including aspirin, should avoid the use of this medication unless they have consulted with a physician. This precaution is essential to prevent potential allergic reactions.

No specific drug or laboratory test interactions have been identified in the available data. Therefore, routine monitoring or dosage adjustments related to drug interactions are not necessary. However, healthcare providers should remain vigilant and consider individual patient circumstances when prescribing this medication.

Packaging & NDC

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

Packaging configurations for Coralite Pain Relief Stick.
Details

Pediatric Use

Pediatric patients under 10 years of age should consult a healthcare professional prior to use. It is important to assess the appropriateness of treatment and dosage for this age group, as specific recommendations may vary based on individual health needs and conditions.

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

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 considered in these populations to ensure the safety of both the mother and the fetus or infant.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is no specific data available regarding the excretion of this medication in 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 information regarding overdosage, healthcare professionals are advised to exercise caution and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the amount and timing of the substance taken, is crucial for effective treatment and follow-up care.

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 in these areas limits the understanding of the compound's potential effects in nonclinical settings.

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. In the event of accidental ingestion, patients should seek medical assistance or contact a Poison Control Center immediately.

Patients should be instructed to discontinue use and consult a healthcare professional if their condition worsens, if symptoms persist for more than 7 days, if symptoms resolve and then recur within a few days, if redness is observed, or if any irritation develops.

When using this product, patients must be reminded to follow the directions carefully. They should avoid bandaging the area tightly or using a heating pad in conjunction with the product. Additionally, patients should be cautioned against contact with the eyes and mucous membranes, and they should not apply the product to wounds or damaged skin.

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 at a controlled temperature range of 20° to 25°C (68° to 77°F) to maintain its integrity and efficacy. Proper storage conditions must be adhered to, ensuring that the product is kept within the specified temperature limits to prevent degradation.

Additional Clinical Information

The product is administered topically. For adults and children aged 10 years and older, it is recommended to apply the medication generously to the affected area, massaging it into the skin until fully absorbed. This application may be repeated as necessary, but should not exceed four times daily. For children under 10 years of age, consultation with a doctor is advised prior to use.

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 Coralite Pain Relief Stick, 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 Stick, 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.