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Pasmol Pain Relieving

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This product has been discontinued

Active ingredients
  • Menthol 5 g/100 g
  • Methyl Salicylate 14 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2015
Label revision date
April 8, 2015
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol 5 g/100 g
  • Methyl Salicylate 14 g/100 g
Other brand names
Dosage form
Cream
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 2015
Label revision date
April 8, 2015
Manufacturer
Grafor, Inc.
Registration number
part348
NDC root
61361-820
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

PASMOL is a pain-relieving ointment designed to provide temporary relief from minor aches and pains in the muscles and joints. It is particularly effective for conditions such as arthritis, simple backache, bruises, and sprains. This ointment is formulated to help soothe discomfort and support your mobility, making it a helpful option for managing everyday pain.

Uses

You can use this medication for the temporary relief of minor aches and pains in your muscles and joints. It is effective for conditions such as arthritis, simple backache, bruises, and sprains. This means if you're dealing with discomfort from these issues, this medication may help alleviate your pain and improve your comfort.

It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) associated with this medication, so it is considered safe in that regard.

Dosage and Administration

If you are an adult or a child aged three years and older, you can apply the medication to the affected area up to three to four times a day. Make sure to follow this guideline to ensure the best results.

If your child is under three years old, it’s important to consult a doctor before using this medication. They can provide specific advice tailored to your child's needs. Always remember to use the medication as directed for safe and effective treatment.

What to Avoid

It's important to use this product safely. You should never apply it to your eyes, mucous membranes (the moist tissue lining certain body parts), or on any wounds or damaged skin. Following these guidelines will help ensure your safety and the effectiveness of the product. If you have any questions or concerns about its use, please consult a healthcare professional.

Side Effects

When using this product, it's important to apply it only to the skin and avoid contact with your eyes, mucous membranes, or any wounds and damaged skin. You should not bandage the area tightly. If your condition worsens, symptoms last more than 7 days, or if you notice redness or excessive skin irritation, stop using the product and consult a doctor.

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

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to your eyes, mucous membranes, or any wounds and damaged skin. When using the product, make sure not to bandage the area too tightly.

If your condition worsens, symptoms last longer than 7 days, or if they clear up and then return within a few days, stop using the product and consult your doctor. Additionally, if you notice any redness or excessive skin irritation, it's important to seek medical advice.

In case of accidental ingestion, seek emergency medical help immediately or contact a Poison Control Center. Your safety is a priority, so please take these precautions seriously.

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. Acting quickly can make a significant difference in the outcome.

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, it’s always better to be safe and get checked by a medical professional.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be aware that there is no specific information available regarding the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions have not been established.

Before taking this medication, you should consult with your healthcare provider to discuss any potential risks and to ensure that you are making informed decisions for your health and the health of your baby. Always prioritize open communication with your doctor about any medications you are considering during pregnancy.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the effects of this medication on nursing mothers or lactation (the process of producing breast milk). Since there are no guidelines or data provided, it’s advisable to consult your healthcare provider for personalized advice and to discuss any potential risks or concerns related to your situation. Your healthcare provider can help you make informed decisions that prioritize both your health and your baby's well-being.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For children aged three years and older, you can apply it to the affected area up to 3-4 times a day. However, if your child is under three years old, you should consult a doctor before using it. This ensures that the treatment is safe and appropriate for their age. Always prioritize your child's health by seeking professional advice when needed.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. Since older adults may have different health needs and may be taking multiple medications, it’s always a good idea to consult with a healthcare provider before starting any new medication. They can help ensure that the treatment is safe and appropriate for your individual health situation.

If you or a loved one is an older adult, be sure to discuss any concerns or questions with your doctor, especially regarding potential interactions with other medications or existing health conditions.

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 or tests you may be taking. In this case, there are no known drug interactions or laboratory test interactions associated with the medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective for you. Always feel free to ask questions and share your complete list of medications and any tests you may be undergoing.

Storage and Handling

To ensure the best quality and safety of your product, store it at room temperature and keep the container tightly closed. It's important to protect the product from light to maintain its effectiveness. Once you open the container, please remember to discard it after use to avoid any potential contamination or degradation. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should apply this medication topically to the affected area, using it no more than 3 to 4 times a day if you are an adult or a child aged three years and older. If the patient is under three years old, it's important to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is PASMOL?

PASMOL is a pain-relieving ointment used for the temporary relief of minor aches and pains of the muscles and joints.

What conditions can PASMOL help relieve?

PASMOL is indicated for minor aches and pains associated with arthritis, simple backache, bruises, and sprains.

How should I use PASMOL?

Apply PASMOL to the affected area not more than 3-4 times daily for adults and children three years of age and older. Consult a doctor for children under 3 years.

Are there any contraindications for using PASMOL?

There are no specified contraindications, but do not use PASMOL in the eyes, on mucous membranes, or on wounds or damaged skin.

What should I do if I experience side effects?

Stop using PASMOL and consult a doctor if your condition worsens, symptoms persist for more than 7 days, or if excessive skin irritation occurs.

Is PASMOL safe to use during pregnancy or while nursing?

No specific information is provided regarding the use of PASMOL during pregnancy or nursing. Consult your doctor for advice.

What should I do if PASMOL is swallowed?

If PASMOL is swallowed, seek medical help or contact a Poison Control Center immediately.

How should I store PASMOL?

Store PASMOL at room temperature, keep the container tightly closed, and protect it from light. Discard after opening.

Packaging Info

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

Packaging configurations for Pasmol Pain Relieving.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

PASMOL is a pain-relieving ointment formulated specifically for the management of arthritis symptoms. It is marketed under the name "Arthritis Formula" and is also known as "Formula Artritis." The product is available in a net weight of 3 oz (85 g).

Uses and Indications

This drug is indicated for the temporary relief of minor aches and pains of the muscles and joints associated with various conditions, including arthritis, simple backache, bruises, and sprains.

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

Dosage and Administration

For adults and children aged three years and older, the recommended application is to the affected area not more than three to four times daily. It is essential to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

For children under three years of age, it is advised to consult a healthcare professional prior to use to determine the appropriate course of action.

Contraindications

Use of this product is contraindicated in the following situations:

The product should not be applied to the eyes, as it may cause irritation or damage. Additionally, it is contraindicated for use on mucous membranes due to the potential for adverse reactions. Application on wounds or damaged skin is also prohibited, as this may lead to further complications or hinder the healing process.

Warnings and Precautions

This product is intended for external use only. It is imperative that it not be applied in or around the eyes, on mucous membranes, or on wounds or damaged skin to prevent adverse reactions.

When utilizing this product, it is crucial to avoid tightly bandaging the area of application, as this may exacerbate potential side effects or hinder the product's effectiveness.

Healthcare professionals should advise patients to discontinue use and seek medical attention if any of the following occur: the condition worsens, symptoms persist for more than 7 days, symptoms resolve and then recur within a few days, redness appears, or if excessive skin irritation develops. These signs may indicate a need for further evaluation and management.

In the event of accidental ingestion, immediate medical assistance should be sought, or the individual should contact a Poison Control Center without delay to ensure appropriate care is provided.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is contraindicated for application in the eyes, on mucous membranes, or on wounds or damaged skin. When using this product, patients are advised not to bandage the area tightly.

In the event that the condition worsens, symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days, patients should discontinue use and consult a doctor. Additionally, if redness or excessive irritation of the skin develops, it is recommended to stop use and seek medical advice.

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

Drug Interactions

No drug interactions or drug and laboratory test interactions have been identified in the available data. Therefore, no specific recommendations for dosage adjustments or monitoring are necessary at this time.

Packaging & NDC

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

Packaging configurations for Pasmol Pain Relieving.
Details

Pediatric Use

Pediatric patients aged three years and older may apply the medication to the affected area no more than 3-4 times daily. For children under three years of age, it is advised to consult a doctor prior to 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 potential adverse effects or changes in therapeutic response, given the lack of targeted data for this population.

Pregnancy

There is no specific information regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. It is advisable to weigh the potential benefits against any unknown risks to fetal outcomes. Women of childbearing potential should be counseled on the importance of effective contraception during treatment and the need to inform their healthcare provider if they become pregnant or plan to become pregnant while on this medication.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established.

Renal Impairment

Patients with renal impairment may not have specific information regarding dosage adjustments, special monitoring, or safety considerations outlined in the prescribing information. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment and individualized patient assessment. Regular monitoring of renal function is advisable to ensure patient safety and therapeutic efficacy.

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 use of the compound in question. Further studies may be necessary to elucidate these aspects of nonclinical toxicology.

Postmarketing Experience

Adverse events have been reported voluntarily to Grafor Inc. through various channels, including surveillance programs. These reports contribute to the ongoing assessment of the product's safety profile in the postmarketing setting.

Patient Counseling

Healthcare providers should advise patients to seek immediate medical assistance or contact a Poison Control Center if the product is swallowed. It is important to instruct patients not to use the product in or around the eyes, on mucous membranes, or on wounds or damaged skin.

Patients should be informed to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, they should be cautioned to stop use and seek medical advice if they notice any redness or if excessive skin irritation develops.

While using this product, patients should be reminded not to apply a tight bandage over the area of application.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature, away from direct light to protect its quality. Once opened, the product should be discarded to ensure safety and efficacy.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3-4 times daily for adults and children aged three years and older. For children under three years of age, it is advised to consult a doctor prior to use. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Pasmol Pain Relieving, 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 Pasmol Pain Relieving, 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

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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.