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Artridon

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Active ingredients
  • Menthol, Unspecified Form 2 g/100 g
  • Methyl Salicylate 15 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
January 7, 2026
Active ingredients
  • Menthol, Unspecified Form 2 g/100 g
  • Methyl Salicylate 15 g/100 g
Other brand names
Dosage form
Ointment
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
January 7, 2026
Manufacturer
Pharmadel LLC
Registration number
M017
NDC root
55758-030

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Drug Overview

Artridone glucosamine PDP is a medication designed to provide temporary relief from minor aches and pains in your muscles and joints. It can be particularly helpful for conditions such as simple backaches, arthritis, strains, bruises, and sprains.

This product works by targeting discomfort in the affected areas, allowing you to feel more comfortable and maintain your daily activities. If you're experiencing any of these minor aches, Artridone glucosamine PDP may be a suitable option for you.

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 manage these specific types of pain.

Dosage and Administration

If you are 12 years old or older, you can apply this medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results. However, if you are under 12 years of age, it’s important not to use this medication without first consulting a doctor. Always prioritize safety and seek professional advice if you have any questions or concerns about using this treatment.

What to Avoid

It's important to use this medication safely to ensure your well-being. You should avoid applying it on wounds or damaged skin, as this can lead to complications. Additionally, do not bandage the area tightly after application, as this may interfere with the medication's effectiveness and could cause irritation.

By following these guidelines, you can help ensure that you use the medication properly and minimize any potential issues. If you have any questions or concerns about your treatment, don't hesitate to reach out to your healthcare provider for guidance.

Side Effects

When using this product, it's important to apply it only to intact skin and avoid contact with your eyes. You should not use it on wounds or damaged skin, and avoid tightly bandaging the area. If your condition worsens, if symptoms last more than 7 days, or if they clear up and then return within a few days, stop using the product and consult a doctor.

If you are pregnant or breastfeeding, please consult a healthcare professional before using this product. Keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center right away.

Warnings and Precautions

This product is for external use only, so be sure to avoid getting it in your eyes. Do not apply it to any wounds or damaged skin, and avoid wrapping the area tightly with a bandage. If your condition worsens or if symptoms last more than 7 days, or if they clear up and then return within a few days, stop using the product and consult your doctor.

If you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this product. Keep it out of reach of children, and if it is swallowed, seek medical help or contact a Poison Control Center right away.

Overdose

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

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for you. If you notice anything concerning, don’t hesitate to get help. Remember, acting quickly can make a significant difference in ensuring safety and health.

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, it's important not to use this medication without first consulting a doctor. For those aged 12 and older, you can apply the medication to the affected area, but be sure to do this no more than 3 to 4 times a day. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

While there is no specific information about how this medication should be used by 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 discuss any concerns with your healthcare provider. They can help determine the best approach for you, considering any potential risks or interactions with other treatments you may be using.

If you or a loved one is an older adult, make sure to keep your healthcare team informed about all medications and health conditions to ensure safe and effective care.

Renal Impairment

If you have kidney problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or safety considerations for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help monitor your kidney function and make any necessary adjustments to your treatment plan.

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 (issues with liver function).

Before starting any new medication, including this one, you should discuss your liver health with your healthcare provider. They can help determine the best approach for your treatment and ensure your safety.

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 share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance of your product, store it in a cool, dry place at a temperature between 68-77°F (20-25°C). This helps maintain its effectiveness and safety.

Before using the product, check the foil seal under the cap. If it is broken, torn, or missing, do not use the product, as this could compromise its safety and effectiveness. Always handle the product with care to ensure it remains in good condition.

Additional Information

No further information is available.

FAQ

What is Artridone glucosamine PDP used for?

Artridone glucosamine PDP is used for the temporary relief of minor aches and pains of muscles and joints associated with simple backaches, arthritis, strains, bruises, and sprains.

How should I apply Artridone glucosamine PDP?

Adults and children 12 years of age and older should apply it to the affected area not more than 3 to 4 times daily. Children under 12 years of age should not use it without consulting a doctor.

Are there any contraindications for using Artridone glucosamine PDP?

There are no contraindications listed for Artridone glucosamine PDP.

What should I avoid while using this product?

You should avoid applying it on wounds or damaged skin and do not bandage tightly. It is for external use only and should not come into contact with the eyes.

What should I do if my condition worsens?

You should stop using the product and ask a doctor if your condition worsens or if symptoms persist for more than 7 days or return after clearing up.

Is it safe to use Artridone glucosamine PDP during pregnancy or breastfeeding?

If you are pregnant or breastfeeding, you should ask a health professional before using Artridone glucosamine PDP.

How should I store Artridone glucosamine PDP?

Store Artridone glucosamine PDP between 68-77°F (20-25°C) and do not use it if the foil seal under the cap is broken, torn, or missing.

What should I do if Artridone glucosamine PDP is swallowed?

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

Packaging Info

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

Packaging configurations for Artridon.
Details

Drug Information (PDF)

This file contains official product information for Artridon, 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 the temporary relief of minor aches and pains of muscles and joints associated with simple backaches, arthritis, strains, bruises, and sprains.

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

Dosage and Administration

For adults and children aged 12 years and older, the recommended application is to the affected area not more than 3 to 4 times daily. It is important to ensure that the application is performed with clean hands and that the affected area is clean and dry prior to application.

For children under 12 years of age, the product should not be used without consulting a healthcare professional.

Contraindications

The product is contraindicated for application on wounds or damaged skin due to the potential for irritation and impaired healing. Additionally, it should not be used with tight bandaging, as this may lead to compromised circulation and increased risk of adverse effects.

Warnings and Precautions

For external use only; contact with the eyes should be avoided. The product must not be applied to wounds or damaged skin, and it is important to refrain from tightly bandaging the area of application.

Healthcare professionals should advise patients to discontinue use and seek medical advice if the condition worsens. Additionally, if symptoms persist for more than 7 days or if they resolve and then recur within a few days, patients should be instructed to consult a physician.

In cases of pregnancy or breastfeeding, it is essential for individuals to consult a healthcare professional prior to use.

This product should be kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center is recommended.

Side Effects

Patients using this product should be aware that it is for external use only and must avoid contact with the eyes. It is advised not to apply the product on wounds or damaged skin, and to refrain from tightly bandaging the area after application.

In clinical practice, patients are instructed to stop use and consult a healthcare professional if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days.

For pregnant or breastfeeding individuals, it is recommended to seek advice from a health professional prior to use. Additionally, this product should be kept 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.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 Artridon (menthol, methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Artridon.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this medication without consulting a doctor. For adolescents and adults aged 12 years and older, the recommended application is to the affected area no more than 3 to 4 times daily.

Geriatric Use

There is no specific information regarding the use of this medication in geriatric patients, including dosage adjustments, safety concerns, or special precautions. Healthcare providers should exercise caution when prescribing this medication to elderly patients, as individual responses may vary. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

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 the safety of both the mother and the developing fetus.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data on the excretion of this drug 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 drug insert regarding dosage adjustments, special monitoring, or safety considerations. 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. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to 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 intervention is crucial. If the substance is ingested, healthcare professionals should advise patients or caregivers to seek medical assistance without delay. Contacting a Poison Control Center is strongly recommended to ensure appropriate management and guidance.

Symptoms of overdosage may vary depending on the specific substance involved; therefore, a thorough assessment by a medical professional is essential. Prompt recognition of symptoms can facilitate timely treatment and improve patient outcomes.

Management of overdosage should be conducted in a clinical setting, where healthcare providers can monitor the patient closely and implement necessary interventions based on the severity of symptoms and the specific circumstances of the overdose.

Nonclinical Toxicology

There is currently no available information regarding teratogenic or non-teratogenic effects associated with the compound. Additionally, no data has been provided concerning nonclinical toxicology, including animal pharmacology and toxicology. As such, the assessment of these aspects remains incomplete.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. In the event of swallowing the product, patients should seek medical assistance or contact a Poison Control Center immediately.

Patients should be instructed to discontinue use and consult a doctor if their condition worsens. Additionally, they should be informed to stop using the product and seek medical advice if symptoms persist for more than 7 days or if symptoms clear up and then recur within a few days.

It is important to inform patients that when using this product, they should avoid applying it on wounds or damaged skin. Furthermore, patients should be cautioned against bandaging the area tightly while using the product to ensure safety and effectiveness.

Storage and Handling

The product is supplied in a configuration that includes a foil seal under the cap. It is essential to inspect this seal prior to use; the product should not be utilized if the foil seal is broken, torn, or missing.

For optimal storage, the product must be kept in a controlled environment with a temperature range of 68-77°F (20-25°C). Proper handling and storage conditions are crucial to maintain the integrity and efficacy of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Artridon, 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 Artridon, 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.

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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.