Symptom checker
Select audience type

Switch between content for healthcare professionals (PRO) and general audience (GEN).

ADD CONDITION

items per page

Pain Relieving Plaster

Last content change checked dailysee data sync status

This product has been discontinued

Active ingredients
  • Camphor (synthetic) 3.1 g/100 g
  • Menthol 2.6 g/100 g
  • Methyl Salicylate 2 g/100 g
Other brand names
Dosage form
Plaster
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
July 3, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Camphor (synthetic) 3.1 g/100 g
  • Menthol 2.6 g/100 g
  • Methyl Salicylate 2 g/100 g
Other brand names
Dosage form
Plaster
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
July 3, 2024
Manufacturer
Health Body World Supply Inc.
Registration number
M014
NDC root
81980-727
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 product is a pain-relieving plaster designed to provide temporary relief from minor aches and pains in muscles and joints. You can use it for various conditions, including simple backache, arthritis, strains, bruises, and sprains. The plaster works by delivering soothing relief directly to the affected area, helping you feel more comfortable and active.

Uses

If you're dealing with minor aches and pains in your muscles and joints, this medication can help provide temporary relief. It's effective for various conditions, including simple backaches, arthritis, strains, bruises, and sprains.

You can rely on this treatment to ease discomfort and help you get back to your daily activities. Remember, it's designed for short-term use to alleviate those nagging pains that can disrupt your routine.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can apply one or two plasters to the affected area once a day. Make sure to remove the plasters after 12 hours. This method helps target the area that needs treatment effectively.

For children aged 2 to 12 years or adults with compromised health, it's important to use this treatment only under the guidance of a doctor. If your child is under 2 years old, do not use this treatment without consulting a doctor first. Always prioritize safety and seek professional advice when needed.

What to Avoid

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

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence (a condition where your body becomes reliant on a substance). However, always follow the guidance provided to ensure safe use.

Side Effects

This product is intended for external use only and contains natural rubber latex, which may cause allergic reactions in some individuals. You should avoid using it on wounds or irritated skin, especially if the product's appearance has changed. If you have known sensitivities to this product or are pregnant, consult your doctor or pharmacist before use.

While using this product, be careful to avoid contact with your eyes and mucous membranes. Do not apply it tightly or use heat sources like heating pads, as this can lead to serious burns. If your condition worsens, symptoms last more than 7 days, or if you experience excessive skin irritation, stop using the product and seek medical advice. Additionally, if you are using it for arthritis pain and it persists for more than 10 days or if redness appears, consult a healthcare professional.

Warnings and Precautions

This product is for external use only and contains natural rubber latex, which can cause allergic reactions. Please avoid using it on wounds or irritated skin, especially if the product's appearance has changed. If you have known allergies to this product or if you are pregnant or taking other medications, consult your doctor or pharmacist before use. While using the product, keep it away from your eyes and mucous membranes, do not apply heat to the area, and avoid tight bandaging.

You should stop using the product and contact your doctor if your condition worsens, if symptoms last longer than 7 days, or if they clear up and then return within a few days. Additionally, if you experience excessive skin irritation, or if you are using it for arthritis pain that persists for more than 10 days or is accompanied by redness, seek medical advice. For children under 12, consult a doctor before use. If the product is swallowed, seek emergency medical help or contact a Poison Control Center immediately.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general 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 always better to be safe and get checked by a healthcare professional if you have any concerns about your health. Remember, timely intervention can make a significant difference.

Pregnancy Use

If you are pregnant or planning to become pregnant, it’s important to consult with your doctor or pharmacist 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 professional advice.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks it may pose to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If your child is under 2 years old, it's important not to use this medication without consulting a doctor first. For children aged 2 to 12 years, you should only use it under a doctor's guidance, especially if they have any health issues.

For children 12 years and older, you can apply one or two plasters to the affected area once a day, and they should be removed after 12 hours. If your child under 12 is experiencing arthritis pain, seek medical advice if the pain lasts more than 10 days, if there is any redness, or if they have other concerning symptoms. Always prioritize your child's health and consult a healthcare professional when in doubt.

Geriatric Use

If you are an older adult or a caregiver, it's important to follow specific guidelines when using this medication. For adults and children aged 12 and older, you should apply one or two plasters to the affected area once a day and remove them after 12 hours.

However, if you are caring for a child aged 2 to 12 or an adult with health issues, it's crucial to consult a doctor before use. This ensures that the treatment is safe and appropriate for their specific health needs. Always prioritize safety and seek professional advice when necessary.

Renal Impairment

If you have kidney 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 for the medication do not change based on renal impairment. However, it’s always best to consult with your healthcare provider about your kidney health and any medications you are taking. They can provide personalized advice and ensure that your treatment is safe and effective for you.

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 tests to ensure your safety while using any medication. Your well-being is a priority, so don't hesitate to ask questions or express any concerns you may have.

Drug Interactions

It's important to talk to your doctor or pharmacist before using this medication, especially if you are taking other medications. This is to ensure that there are no potential interactions that could affect how well your treatments work or increase the risk of side effects. Always keep your healthcare provider informed about all the medications you are currently using to help them provide you with the safest and most effective care.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Once you open the product, be sure to discard it after use to maintain safety and quality. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

For adults and children aged 12 and older, you should apply one or two plasters to the affected area once a day and remove them after 12 hours. If you are using this treatment for children aged 2 to 12 or for adults with compromised health, it's important to do so under the guidance of a doctor. Additionally, do not use this treatment for children under 2 years of age without consulting a doctor first.

FAQ

What is this drug used for?

This drug is a pain relieving plaster used for the temporary relief of minor aches and pains of muscles and joints due to conditions like simple backache, arthritis, strains, bruises, and sprains.

Who can use this plaster?

Adults and children 12 years of age and older can use it. Children aged 2 to 12 and adults with compromised health should use it only under a doctor's guidance, while it is not recommended for children under 2 years of age.

How should I apply the plaster?

You should apply one or two plasters to the affected area once a day and remove them after 12 hours.

Are there any warnings I should be aware of?

Yes, this product is for external use only and contains natural rubber latex, which may cause allergic reactions. Avoid using it on wounds or irritated skin, and do not apply heat to the area.

What should I do if I experience irritation or if my condition worsens?

You should stop using the plaster and consult a doctor if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation develops.

What should I do if I accidentally swallow the plaster?

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

Can I use this plaster if I am pregnant?

You should ask a doctor or pharmacist before using this product if you are pregnant.

How should I store this plaster?

Store the plaster at room temperature, protect it from light, and do not freeze it. Discard it after opening.

Packaging Info

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

Packaging configurations for Pain Relieving Plaster.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is a pain-relieving plaster designed for topical application. It provides localized relief from pain through its active ingredients, which are delivered directly to the affected area. The plaster is formulated to adhere securely to the skin, ensuring prolonged contact and effectiveness. Its design allows for ease of use and convenience in managing pain symptoms.

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains associated with muscles and joints. Specifically, it is effective for conditions such as simple backache, arthritis, strains, bruises, and sprains.

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

Dosage and Administration

Adults and children 12 years of age and older are instructed to apply one or two plasters to the affected area once daily. The plasters should be removed after 12 hours of application.

For children aged 2 to 12 years and adults with compromised health, the use of plasters should only occur under the guidance of a healthcare professional.

The product is contraindicated for use in children under 2 years of age; consultation with a doctor is recommended in such cases.

Contraindications

There are no specific contraindications listed for this product. However, it is imperative to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed.

Warnings and Precautions

For external use only. This product contains natural rubber latex, which may cause allergic reactions. It is imperative that the product not be used on wounds or on irritated or damaged skin, particularly if there has been a change in the appearance of the product. Individuals with known hypersensitivities to this product should refrain from use, as should those who do not follow the directions provided.

Healthcare professionals should advise patients to consult a doctor or pharmacist prior to use if they are currently taking other medications or if they are pregnant. During application, it is crucial to avoid contact with the eyes or mucous membranes. Bandaging should not be done tightly, and the application of heat in the form of heating pads, hot water bottles, or lamps should be strictly avoided due to the risk of serious burns. Additionally, care should be taken to avoid placing the product on extremely hairy areas of skin to prevent irritation upon removal.

Patients should be instructed to discontinue use and seek medical advice if any of the following occur: the condition worsens, symptoms persist for more than 7 days, symptoms resolve only to recur within a few days, excessive skin irritation develops, or if the product is being used for arthritis pain and any of the following occur: pain persists for more than 10 days, redness is present, or if the patient is under 12 years of age.

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

Side Effects

Patients using this product should be aware of several important warnings and precautions. This product is for external use only and contains natural rubber latex, which may cause allergic reactions in some individuals. It is contraindicated for use on wounds or on irritated or damaged skin, particularly if the appearance of the product has changed. Additionally, patients with known hypersensitivities to this product should not use it, and it should only be used as directed.

Before using this product, patients are advised to consult a doctor or pharmacist if they are taking other medications or if they are pregnant. While using the product, it is crucial to avoid contact with the eyes or mucous membranes, not to bandage tightly, and to refrain from applying heat to the area, as this may increase the risk of serious burns. Patients should also avoid placing the product on extremely hairy areas of skin to minimize irritation during removal.

Patients should discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than 7 days, if symptoms resolve and then recur within a few days, or if excessive skin irritation develops. Specifically, when using the product for arthritis pain, patients should stop use if pain persists for more than 10 days, if redness is present, or if the product is being used for conditions affecting children under 12 years of age.

Drug Interactions

Patients are advised to consult a healthcare professional, such as a doctor or pharmacist, prior to using this medication if they are currently taking other medications. This precaution is essential to identify potential drug interactions that may affect the efficacy or safety of treatment.

It is important to monitor for any adverse effects or changes in therapeutic outcomes when combining this medication with others. Adjustments to dosage or additional monitoring may be necessary based on the specific interactions identified during consultation.

Packaging & NDC

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

Packaging configurations for Pain Relieving Plaster.
Details

Pediatric Use

Pediatric patients under 2 years of age should not use this product and must consult a doctor for guidance. For children aged 2 to 12 years and adults with compromised health, use is recommended only under the supervision of a healthcare professional.

In patients aged 12 years and older, the recommended application is one or two plasters to the affected area once daily, with removal after 12 hours. For children under 12 years of age experiencing pain from arthritis, it is advised to seek medical attention if pain persists for more than 10 days, if redness is present, or in any other concerning conditions affecting this age group.

Geriatric Use

Elderly patients, defined as those aged 65 years and older, should be monitored closely when using this medication. For adults and children aged 12 years and older, the recommended application is one or two plasters to the affected area once daily, with removal after 12 hours.

In geriatric patients, particularly those with compromised health, it is advised that the use of this medication occurs only under the guidance of a healthcare provider. This precaution is essential to ensure safety and efficacy, as elderly patients may have altered pharmacokinetics and increased sensitivity to medications. Therefore, careful consideration and monitoring are recommended when prescribing this treatment to the elderly population.

Pregnancy

Pregnant patients should consult a healthcare professional, such as a doctor or pharmacist, before using this medication. The safety of this drug during pregnancy has not been established, and potential risks to fetal outcomes are not fully understood. Therefore, it is essential for women of childbearing potential to seek medical advice prior to use to ensure appropriate risk assessment and management.

Lactation

There are no specific warnings or recommendations regarding the use of this product by lactating mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in 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 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 monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, consultation with a poison control center or a medical toxicologist is recommended to guide further management and intervention strategies.

Documentation of the incident, including the substance involved, the amount taken, and the time of ingestion, 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 limits the assessment of potential risks associated with the use of the compound in these contexts.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Healthcare providers should advise patients that in the event of accidental ingestion, it is crucial to seek medical assistance immediately or contact a Poison Control Center. This prompt action is essential to ensure the safety and well-being of the patient.

Storage and Handling

The product is supplied in packaging that includes specific NDC numbers. It should be stored at room temperature, ensuring that it is protected from light exposure. Freezing the product is not permitted, as it may compromise its integrity. Additionally, once opened, the product must be discarded to maintain safety and efficacy.

Additional Clinical Information

For patients aged 12 years and older, the recommended administration involves applying one or two plasters to the affected area once daily, with removal after 12 hours. For children aged 2 to 12 years and adults with compromised health, usage should occur only under a physician's guidance. The product is contraindicated for children under 2 years of age, and consultation with a doctor is advised for this age group.

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 Pain Relieving Plaster, 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 Pain Relieving Plaster, 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.