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Meijer Ultra Strength Pain Relieving

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Active ingredients
  • Menthol, Unspecified Form 100 mg/1 g
  • Camphor (synthetic) 40 mg/1 g
  • Methyl Salicylate 300 mg/1 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 2020
Label revision date
November 15, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Menthol, Unspecified Form 100 mg/1 g
  • Camphor (synthetic) 40 mg/1 g
  • Methyl Salicylate 300 mg/1 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 2020
Label revision date
November 15, 2024
Manufacturer
Meijer Distribution, Inc
Registration number
M017
NDC root
79481-1220
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

Meijer® Ultra Strength pain relieving cream is a topical product designed to provide temporary relief from minor aches and pains in muscles and joints. It contains active ingredients such as camphor (4%), menthol (10%), and methyl salicylate (30%), which work together to soothe discomfort associated with conditions like arthritis, simple backaches, strains, sprains, and bruises.

This non-greasy cream is easy to apply and is formulated to help you manage pain effectively, allowing you to continue with your daily activities with greater comfort.

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 discomfort associated with conditions like arthritis, simple backaches, strains, sprains, and bruises.

You can rely on this treatment to ease your pain and help you get back to your daily activities. Remember, it's designed for short-term use to manage these specific types of discomfort.

Dosage and Administration

If you are an adult or a child aged 12 years and 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.

For children under 12 years of age, it’s important to consult a doctor before use. This will help ensure that the medication is safe and appropriate for their specific needs. Always follow your healthcare provider's advice for the best care.

What to Avoid

It's important to use this medication safely. You should not use it for arthritis-like conditions in children under 12 without consulting a doctor. Avoid using it with a heating pad, on wounds, or on damaged skin.

Additionally, do not swallow the medication or bandage the area tightly. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

If you have a history of allergic reactions to aspirin or salicylates, it's important to consult your doctor before using this product. Avoid getting it in your eyes or on mucous membranes. This product should not be used for arthritis-like conditions in children under 12, with a heating pad, or on wounds and damaged skin.

While using this product, follow the directions carefully. Do not swallow it or apply a tight bandage. If your condition worsens, or if symptoms last more than 7 days or return after improvement, stop using it and consult your doctor. Keep this product out of reach of children, and if swallowed, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

Warnings and Precautions

This product is for external use only, so please avoid swallowing it. If you have a history of allergic reactions to aspirin or salicylates, consult your doctor before using it. Be careful to keep it away from your eyes and mucous membranes, and do not apply it to wounds or damaged skin. If you are pregnant or breastfeeding, it's important to talk to a healthcare professional before using this product.

When using this product, follow the instructions carefully. Do not use it with a heating pad or bandage the area tightly. If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and contact your doctor. Always keep this product out of reach of children, and if it is swallowed, seek medical help immediately or call Poison Control at 1-800-222-1222.

Overdose

If you or someone else has swallowed too much of this medication, it’s important to seek medical help immediately. You can contact a Poison Control Center at 1-800-222-1222 for guidance.

Signs of an overdose may include unusual symptoms, but specific details about these symptoms are not provided here. If you notice anything concerning, don’t hesitate to reach out for 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

When it comes to using this medication for children, it's important to be cautious. If your child is under 12 years old, you should consult a doctor before giving them this medication. This is especially crucial if your child has arthritis-like conditions, as the medication is not recommended for these issues in children under 12. Always prioritize your child's health by seeking professional advice.

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. As you age, your body may process medications differently, which can affect how well they work and the potential for side effects.

If you or a loved one is considering this medication, it’s wise to discuss it with a healthcare provider. They can help determine if any adjustments are needed based on individual health conditions and ensure that the treatment is safe and effective for older adults. Always prioritize open communication with your healthcare team about any concerns or questions you may have.

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 your kidneys are not functioning properly.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your kidney health. They can help monitor your condition 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 (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 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 at room temperature. This helps maintain its effectiveness and safety. When handling the product, be sure to follow any specific instructions provided to avoid contamination or damage. Always keep the product in a clean environment to ensure it remains safe for use. If you have any questions about disposal or other safety measures, please refer to the guidelines provided with your product.

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 12 years and older. If the patient is under 12 years old, it's important to consult a doctor before use. There are no additional details available regarding laboratory tests, abuse potential, or postmarketing experiences related to this medication.

FAQ

What is meijer® Ultra Strength pain relieving cream used for?

It provides temporary relief of minor aches and pains of muscles and joints associated with conditions like arthritis, simple backache, strains, sprains, and bruises.

What are the active ingredients in this cream?

The active ingredients are Camphor (4%), Menthol (10%), and Methyl Salicylate (30%).

How should I use meijer® Ultra Strength pain relieving cream?

Apply to the affected area not more than 3 to 4 times daily for adults and children 12 years and older. Consult a doctor for children under 12.

Are there any contraindications for using this cream?

Do not use it for arthritis-like conditions in children under 12, with a heating pad, or on wounds or damaged skin.

What should I do if I experience side effects?

Stop use 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 if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, consult a health professional before use.

What should I do if the cream is swallowed?

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Can I use this cream on my face?

Avoid contact with the eyes and mucous membranes when using this product.

Packaging Info

Below are the non-prescription pack sizes of Meijer Ultra Strength Pain Relieving (camphor (synthetic) , menthol, unspecified form, and methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Ultra Strength Pain Relieving.
Details

Drug Information (PDF)

This file contains official product information for Meijer Ultra Strength Pain Relieving, 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 various conditions, including arthritis, simple backache, strains, sprains, and bruises.

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 limited to the specified frequency to avoid potential adverse effects.

For children under 12 years of age, it is advised to consult a healthcare professional prior to use to determine the appropriate course of action and dosage.

Contraindications

Use is contraindicated in the following situations:

  • The product should not be used for arthritis-like conditions in children under 12 years of age; consultation with a healthcare professional is advised.

  • Application with a heating pad is contraindicated due to the potential for increased risk of burns or skin irritation.

  • The product must not be applied to wounds or damaged skin to prevent exacerbation of the injury or infection.

  • Swallowing the product is contraindicated.

  • Tight bandaging of the area where the product is applied is not recommended.

Warnings and Precautions

For external use only. Healthcare professionals should advise patients to consult a doctor if they are prone to allergic reactions from aspirin or salicylates prior to using this product. It is imperative to avoid contact with the eyes and mucous membranes to prevent irritation.

This product is not indicated for use in children under 12 years of age for arthritis-like conditions; a consultation with a healthcare provider is recommended in such cases. Additionally, the application of this product in conjunction with a heating pad is contraindicated, as it may lead to increased risk of adverse effects.

The product should not be applied to wounds or damaged skin, as this may exacerbate irritation or lead to complications. Pregnant or breastfeeding individuals should seek advice from a health professional before using this product to ensure safety for both mother and child.

When utilizing this product, it is essential to adhere strictly to the directions provided. Patients should be instructed not to swallow the product and to avoid tight bandaging of the area of application, as this may hinder proper absorption and increase the risk of side effects.

Patients should be advised to discontinue use and consult a doctor if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days.

It is crucial to keep this product out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact with a Poison Control Center (1-800-222-1222) should be made without delay.

Side Effects

Patients should be aware of potential adverse reactions associated with this product. Individuals with a known allergy to aspirin or salicylates are advised to consult a healthcare professional prior to use. It is important to avoid contact with the eyes and mucous membranes to prevent irritation.

The product is contraindicated for use in children under 12 years of age for arthritis-like conditions, and patients should consult a doctor before use in such cases. Additionally, the product should not be used in conjunction with a heating pad or applied to wounds or damaged skin.

While using this product, it is crucial to adhere strictly to the directions provided. Patients should not swallow the product or apply a tight bandage over the area of application.

Patients are advised 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.

This product should be kept out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted at 1-800-222-1222.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding 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 Meijer Ultra Strength Pain Relieving (camphor (synthetic) , menthol, unspecified form, and methyl salicylate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Ultra Strength Pain Relieving.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this medication for arthritis-like conditions without consulting a healthcare professional. It is essential for caregivers to seek medical advice before administering this treatment to children in this age group.

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 adverse effects or changes in therapeutic response, 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, as the effects on fetal outcomes and breastfeeding infants are not fully established. It is essential for women of childbearing potential to discuss their individual circumstances with a healthcare provider to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a healthcare professional prior to using this medication. There is currently no available data regarding the excretion of this medication 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 no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data may impact the drug's efficacy and safety profile in this population. Regular monitoring of renal function is advisable to ensure patient safety.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to 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 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 without delay. It is recommended to contact a Poison Control Center at 1-800-222-1222 for expert guidance on managing the situation.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Healthcare providers should be prepared to assess the patient's condition and implement appropriate management strategies based on the severity of symptoms and the specific substance involved.

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.

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. Instruct patients that if the product is swallowed, they should seek medical help or contact a Poison Control Center immediately at 1-800-222-1222.

It is important to inform patients that this product should not be used for arthritis-like conditions in children under 12 years of age without consulting a doctor. Additionally, patients should be cautioned against using the product in conjunction with a heating pad, as this may lead to adverse effects.

Patients should also be made aware that the product should not be applied to wounds or damaged skin. They should be instructed to stop using the product 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.

When using this product, patients must be reminded to follow the directions carefully and to avoid swallowing the product. Furthermore, they should not bandage the area tightly after application to ensure safety and effectiveness.

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 room temperature to maintain its integrity and efficacy. No special handling requirements are noted; however, standard precautions should be observed to ensure optimal storage conditions.

Additional Clinical Information

The medication is administered topically, with a recommended application frequency of 3 to 4 times daily for adults and children aged 12 years and older. For children under 12 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 Meijer Ultra Strength 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 Meijer Ultra Strength 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.