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Dr Goldsons Pain

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Active ingredients
  • Menthol 8 g/100 g
  • Methyl Salicylate 30 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2021
Label revision date
December 19, 2024
Active ingredients
  • Menthol 8 g/100 g
  • Methyl Salicylate 30 g/100 g
Other brand names
Dosage form
Cream
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2021
Label revision date
December 19, 2024
Manufacturer
Derma Care Research Labs, LLC
Registration number
M017
NDC root
72839-145

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Drug Overview

This medication is designed to provide temporary relief from minor aches and pains in muscles and joints. It can be particularly helpful for conditions such as simple backache, arthritis, strains, bruises, and sprains. If you're experiencing discomfort from these common issues, this drug may be a suitable option to help ease your 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 simple backache, arthritis, strains, bruises, and sprains. If you're dealing with any of these discomforts, this medication may help ease your symptoms and improve your comfort.

Dosage and Administration

When using this medication, if you are an adult or a child over 12 years old, you should apply it to the affected area no more than 3 to 4 times a day. This helps ensure that you get the best results while minimizing the risk of side effects. If you are caring for a child who is 12 years old or younger, it’s important to consult a doctor before using this medication to ensure it’s safe and appropriate for them.

After each use, make sure to close the cap tightly. This helps keep the medication effective and prevents contamination. Always follow these guidelines to ensure safe and effective use of the product.

What to Avoid

It's important to be aware of certain precautions when using this medication. If you accidentally swallow it, you should seek medical help immediately or contact a Poison Control Center. This is crucial for your safety, as prompt action can help prevent any potential harm.

Currently, there are no specific contraindications, risks of abuse or misuse, or concerns about dependence associated with this medication. However, always use it as directed and consult your healthcare provider if you have any questions or concerns. Your health and safety are the top priority.

Side Effects

When using this product, it's important to be aware of some potential side effects and warnings. You should only use it externally and avoid applying it to wounds or damaged skin. Additionally, steer clear of contact with your eyes or mucous membranes, and do not wrap the area tightly with a bandage.

If you notice that your condition worsens, symptoms last longer than 7 days, or if they improve and then return within a few days, you should stop using the product and consult a doctor. Be cautious of excessive skin irritation as well, and seek medical advice if this occurs.

Warnings and Precautions

This product is intended for external use only, so please avoid applying it to wounds or damaged skin, and do not use it with a heating pad. While using this product, be careful to keep it away from your eyes and mucous membranes, and do not wrap the area tightly with a bandage.

If your condition worsens, if symptoms last longer than 7 days, or if they improve and then return within a few days, stop using the product and consult your doctor. Additionally, if you accidentally swallow the product, seek 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.

Pregnancy Use

There is currently no specific information available about the use of Dr. Goldson's Pain Relief Cream during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions for pregnant individuals have not been addressed in the drug insert.

If you are pregnant or planning to become pregnant, it is important to consult with your healthcare provider before using this product. They can help you understand any potential risks and guide you on the best options for pain relief during this time.

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 the safety and potential impact on your milk production or your baby are not clearly defined, it’s advisable to consult with your healthcare provider for personalized guidance. They can help you weigh the benefits and risks based on your individual situation.

Pediatric Use

If you are considering this medication for a child who is 12 years old or younger, it’s important to consult with a doctor first. This ensures that the treatment is safe and appropriate for your child's specific needs. Always prioritize professional guidance when it comes to the health of your little ones.

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 issues, it's important to know that there are no specific guidelines provided regarding dosage adjustments, special monitoring, or safety considerations for your condition. This means that the information available does not outline any changes you may need to make to your treatment or any additional precautions you should take.

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your kidney health. They can help you understand how your condition may affect your medication and what steps you should take.

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 ensure that any medication you take is safe and appropriate for your liver condition. They can help monitor your liver function and make any necessary adjustments to your treatment plan.

Drug Interactions

It's great to know that there are no identified interactions between this medication and other drugs or laboratory tests. This means that, in general, you can take this medication without worrying about it affecting other treatments or test results.

However, it's still very important to discuss all medications and any lab tests you may be undergoing with your healthcare provider. They can provide personalized advice and ensure that your overall treatment plan is safe and effective. Always keep your healthcare team informed about everything you are taking, including over-the-counter medications and supplements.

Storage and Handling

To ensure the best performance and safety of your product, always store it at room temperature. After each use, make sure to close the cap tightly to prevent contamination and maintain its integrity. Following these simple steps will help you use the product effectively and safely.

Additional Information

You should apply this product to the affected area no more than 3 to 4 times daily if you are an adult or a child over 12 years old. If the user is 12 years or younger, consult a doctor first. Remember, this product is for external use only—do not apply it to wounds or damaged skin, and avoid using it with a heating pad.

While using the product, keep it away from your eyes and mucous membranes, and do not wrap the area tightly. If your condition worsens, symptoms last more than 7 days, or if they clear up and return within a few days, stop using the product and consult a doctor. If swallowed, seek medical help or contact a Poison Control Center immediately. Always use the product as directed and make sure to close the cap tightly after each use.

FAQ

What is the primary use of this drug?

This drug is used for the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

How should adults and children over 12 years use this drug?

Adults and children over 12 years should apply it to the affected area no more than 3 to 4 times daily.

What should children 12 years or younger do before using this drug?

Children 12 years or younger should ask a doctor before use.

Are there any warnings associated with this drug?

Yes, it is for external use only, should not be used on wounds or damaged skin, and you should avoid contact with eyes or mucous membranes.

What should I do if I swallow this drug?

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

What should I do if my condition worsens or symptoms persist?

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

How should I store this drug?

You should store it at room temperature and close the cap tightly after use.

Packaging Info

Below are the non-prescription pack sizes of Dr Goldsons Pain (menthol 8%, methyl salicylate 30%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr Goldsons Pain.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

The product is identified by the SPL code 34089-3. No additional specific description details are provided in the available data.

Uses and Indications

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

There are no teratogenic or nonteratogenic effects mentioned in the available data.

Dosage and Administration

For adults and children over 12 years of age, the recommended application is to the affected area not more than 3 to 4 times daily. For children aged 12 years or younger, it is advised to consult a physician prior to use.

After each application, ensure that the cap is closed tightly to maintain product integrity and prevent contamination.

Contraindications

There are no specific contraindications listed for this product. However, it is advised that if the product is swallowed, immediate medical assistance should be sought or contact with a Poison Control Center should be made.

Warnings and Precautions

This product is intended for external use only. It is imperative that it not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad, as this may lead to adverse effects.

Healthcare professionals should advise patients to avoid contact with the eyes and mucous membranes during application. Additionally, it is important to refrain from tightly bandaging the area where the product is applied, as this may exacerbate potential side effects.

Patients should be instructed to discontinue use and seek medical advice if the condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days. In cases of excessive skin irritation, immediate consultation with a healthcare provider is recommended.

In the event of accidental ingestion, it is crucial to seek medical assistance or contact a Poison Control Center without delay to ensure appropriate management.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is contraindicated for application on wounds or damaged skin and should not be used in conjunction with a heating pad. Care should be taken to avoid contact with the eyes or mucous membranes during use, and bandaging should not be applied 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 are advised to discontinue use and consult a healthcare professional. Additionally, if excessive skin irritation occurs, it is recommended to stop use and seek medical advice.

Drug Interactions

No drug interactions have been identified in the available data. Additionally, there are no interactions noted between drugs and laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

Below are the non-prescription pack sizes of Dr Goldsons Pain (menthol 8%, methyl salicylate 30%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Dr Goldsons Pain.
Details

Pediatric Use

Pediatric patients 12 years of age or younger should consult a healthcare professional before 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

There is no specific information available 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

There is no specific information regarding the use of Dr Goldsons Pain Relief Cream in pregnant patients. The prescribing information does not provide safety concerns, dosage modifications, or special precautions related to its use during pregnancy. Healthcare professionals should consider the lack of data when advising women of childbearing potential and weigh the potential risks and benefits before recommending this product to pregnant patients.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution when prescribing this medication to lactating mothers, as the effects on breastfed infants have not been established. It is advisable to weigh the potential benefits against any unknown risks when considering treatment options for lactating patients.

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 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 consider the potential risks associated with excessive administration of the medication.

Recommended Actions

In the event of suspected overdosage, it is imperative to seek immediate medical attention. Healthcare providers should monitor the patient closely for any adverse effects and initiate appropriate supportive care as necessary.

Potential Symptoms

While specific symptoms of overdosage are not detailed, healthcare professionals should remain vigilant for any unusual or severe reactions that may arise following excessive intake of the medication.

Management Procedures

Management of overdosage should be tailored to the individual patient and may include symptomatic treatment and supportive measures. It is essential to consult local poison control centers or relevant medical authorities for guidance on the management of suspected overdosage cases.

In summary, due to the lack of detailed overdosage information, healthcare professionals must rely on clinical judgment and established protocols to ensure patient safety in cases of suspected overdosage.

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 for SPL code 90375-7.

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 a configuration that requires the cap to be closed tightly after each use to maintain integrity. It should be stored at room temperature to ensure optimal stability and efficacy.

Additional Clinical Information

Patients should apply the product to the affected area no more than 3 to 4 times daily if they are adults or children over 12 years of age. For children 12 years or younger, it is advised to consult a doctor before use.

Clinicians should counsel patients that the product is for external use only and should not be applied to wounds or damaged skin, nor should it be used in conjunction with a heating pad. Patients must avoid contact with eyes and mucous membranes, and should not bandage the area tightly. They should discontinue use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, if symptoms clear and then recur within a few days, or if excessive skin irritation occurs. In the event of ingestion, patients should seek medical assistance or contact a Poison Control Center immediately. It is important to use the product only as directed and to ensure the cap is closed tightly after use.

Drug Information (PDF)

This file contains official product information for Dr Goldsons Pain, 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 Dr Goldsons Pain, 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.