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Meijer Pain Relieving Max Strength with Lavender Essential Oil

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Active ingredient
Lidocaine Hydrochloride 40 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2021
Label revision date
November 15, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 40 mg/1 mL
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Liquid
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 2021
Label revision date
November 15, 2024
Manufacturer
Meijer Distribution, Inc
Registration number
M017
NDC root
79481-0019
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® is a pain-relieving liquid designed to provide temporary relief from discomfort. It features a maximum strength formulation with 4% lidocaine (a local anesthetic that numbs the area) and is enhanced with lavender essential oil for a soothing effect. This product is fast-acting and easy to apply directly to the affected area, thanks to its no-mess applicator.

Whether you're dealing with muscle aches or joint pain, Meijer® offers a convenient solution to help you feel more comfortable.

Uses

You can use this medication for the temporary relief of pain. It is designed to help alleviate discomfort, making it easier for you to go about your daily activities. Rest assured, there are no known teratogenic effects (which means it does not cause birth defects) associated with this medication.

Dosage and Administration

When using this medication, you should apply it to the affected area of your skin no more than 3 to 4 times a day. This applies to both adults and children who are 12 years old and older. If you have a child under 12, it’s important to consult a doctor before using this medication to ensure it’s safe and appropriate for them. Always follow these guidelines to help manage your condition effectively.

What to Avoid

It's important to use this medication safely to avoid potential issues. You should not apply it to large areas of your body or on skin that is cut, irritated, or swollen. Additionally, avoid using it on puncture wounds. Do not cover the treated area with a bandage or apply heat, such as heating pads, and do not use it alongside other topical pain relievers.

Make sure to keep the medication away from your eyes and mucous membranes, as contact can cause irritation. Following these guidelines will help ensure your safety while using this product.

Side Effects

You should only use this product on the skin and avoid applying it to large areas, cut, irritated, or swollen skin, as well as puncture wounds. If you notice any redness or irritation, or if your condition worsens or does not improve after 7 days, stop using it and consult your doctor.

It's important to keep the product away from your eyes and mucous membranes, and do not use it alongside other topical pain relievers. Additionally, avoid using heat on the treated area and keep it away from fire. If you are pregnant or breastfeeding, consult a healthcare professional before use, and always keep it out of reach of children. If swallowed, seek medical help immediately.

Warnings and Precautions

This product is for external use only, so please make sure to follow all directions and warnings on the packaging carefully. Avoid using it on large areas of your body, on broken or irritated skin, or on puncture wounds. It's important not to cover the treated area with bandages or apply heat, such as heating pads, and do not use it alongside other topical pain relievers. Be cautious to keep it away from your eyes and mucous membranes.

If your condition worsens, symptoms last longer than 7 days, or if you notice redness or irritation, stop using the product and consult your doctor. In case of accidental swallowing, seek emergency medical help or contact a Poison Control Center at 1-800-222-1222 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 contact a Poison Control Center at 1-800-222-1222 for immediate assistance.

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

If your child is under 12 years old, it's important to consult a doctor before using this medication. For children aged 12 and older, you can apply the medication to the affected area, but be sure not to exceed 3 to 4 applications in a day. Always follow these guidelines to ensure your child's safety and well-being.

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, and factors like kidney function (renal impairment) and changes in cognition can affect how well a drug works or how it may impact you.

If you are an older adult or a caregiver, it’s wise to discuss any medications with your healthcare provider. They can help determine the best approach for your individual health needs and ensure that any potential risks are managed effectively. Always prioritize open communication with your doctor about any concerns or questions you may have regarding medications.

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 include special monitoring or safety considerations tailored for patients with renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that your treatment plan is safe and effective for your specific health needs. They can help determine the best approach based on your kidney function and overall health.

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 condition and the use of this medication. They can help ensure that you receive the safest and most effective treatment.

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 feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

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 specific handling procedures, please refer to the guidelines provided with your product.

Additional Information

You should apply this medication to the affected area no more than 3 to 4 times daily if you are an adult or a child aged 12 years or older. If your child is under 12, consult a doctor before use.

If you are pregnant or breastfeeding, it's important to ask a health professional before using this product. Always keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center at 1-800-222-1222 immediately.

FAQ

What is meijer®?

Meijer® is a pain relieving liquid designed for the temporary relief of pain.

What are the key ingredients in meijer®?

Meijer® contains 4% Lidocaine, which is a local anesthetic, and Lavender Essential Oil.

How should I use meijer®?

Apply meijer® 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 warnings for using meijer®?

Yes, it is for external use only. Avoid using it on large areas, cut or irritated skin, and do not allow contact with eyes or mucous membranes.

What should I do if I experience irritation or redness?

Discontinue use and consult a doctor if irritation develops or if redness is present.

Can I use meijer® while pregnant or breastfeeding?

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

What should I do if meijer® is swallowed?

If swallowed, get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

How should meijer® be stored?

Store meijer® at room temperature.

Packaging Info

Below are the non-prescription pack sizes of Meijer Pain Relieving Max Strength with Lavender Essential Oil (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Pain Relieving Max Strength with Lavender Essential Oil.
Details

Drug Information (PDF)

This file contains official product information for Meijer Pain Relieving Max Strength with Lavender Essential Oil, 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 drug.

Uses and Indications

This drug is indicated for the temporary relief of pain.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

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 essential to ensure that the application is performed with clean hands and that the affected area is clean and dry prior to administration.

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

Contraindications

Use is contraindicated in the following situations:

Application on large areas of the body, or on cut, irritated, or swollen skin is not recommended due to the potential for increased absorption and adverse effects. The product should not be applied to puncture wounds to avoid complications associated with improper use.

Contact with eyes or mucous membranes must be avoided to prevent irritation or injury. Additionally, concurrent use with other topical analgesics is contraindicated to reduce the risk of additive effects and potential toxicity.

Local heat application, including the use of heating pads, and bandaging of the treated area are also contraindicated, as these practices may enhance absorption and lead to systemic effects.

Warnings and Precautions

For external use only. This product should be utilized strictly as directed. Healthcare professionals are advised to ensure that patients read and adhere to all instructions and warnings provided on the packaging.

It is imperative to avoid application on large areas of the body or on cut, irritated, or swollen skin. The product should not be applied to puncture wounds. Additionally, patients should refrain from bandaging the area of application or applying local heat, such as heating pads, and should not use it in conjunction with a medicated patch. Care must be taken to prevent contact with the eyes or mucous membranes, and concurrent use with other topical analgesics is contraindicated.

Patients should be instructed to discontinue use and consult a healthcare provider 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 is observed, or irritation develops.

In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center (1-800-222-1222) should be contacted without delay.

Side Effects

Patients should be aware that the product is intended for external use only. It is crucial to discontinue use and consult a healthcare professional if the condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. Additionally, patients should seek medical advice if redness or irritation develops during use.

The product should not be applied to large areas of the body, nor should it be used on cut, irritated, or swollen skin. It is contraindicated for use on puncture wounds. Patients are advised against bandaging the area of application or applying local heat, such as heating pads, and should not use the product concurrently with other topical analgesics. Care should be taken to avoid contact with the eyes or mucous membranes.

Patients should also be informed to keep the product away from fire or flame. Pregnant or breastfeeding individuals are encouraged to consult a healthcare professional before use. Furthermore, the 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 (1-800-222-1222) should be made.

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 necessary at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Meijer Pain Relieving Max Strength with Lavender Essential Oil (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Pain Relieving Max Strength with Lavender Essential Oil.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a doctor before use. For adolescents and children aged 12 years and older, the recommended application is to the affected area not more than 3 to 4 times daily.

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. It is important to assess the potential risks and benefits, as well as any available data regarding fetal outcomes and lactation. Healthcare providers can offer guidance tailored to individual circumstances, ensuring the safety of both the patient and the developing fetus or nursing infant.

Lactation

Lactating mothers are advised to consult a healthcare professional prior to using this medication. There is no specific data available regarding the excretion of this medication in 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 prescribing information 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 and monitoring of these patients.

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 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.

Prompt intervention is essential to mitigate potential adverse effects associated with overdosage. Symptoms may vary depending on the specific substance involved, and healthcare providers should be prepared to assess and manage these symptoms accordingly.

Management procedures may include supportive care and symptomatic treatment, tailored to the individual patient's needs. Continuous monitoring and evaluation are recommended to ensure patient safety and effective recovery.

Nonclinical Toxicology

If pregnant or breastfeeding, individuals are advised to consult a health professional prior to use. No non-teratogenic effects have been specified in the available data. Additionally, there are no details provided regarding nonclinical toxicology or animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are provided in the insert.

Patient Counseling

Patients should be advised to keep this product out of reach of children. In the event of accidental ingestion, they should seek medical assistance or contact a Poison Control Center immediately at 1-800-222-1222.

Patients must be informed to discontinue use and consult a healthcare provider if their condition worsens, if symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days. They should also seek medical advice if they notice any redness or if irritation develops.

When using this product, patients should use it only as directed and read all directions and warnings on the carton carefully. They should be cautioned against using the product on large areas of the body or on cut, irritated, or swollen skin, as well as on puncture wounds. Additionally, patients should not bandage or apply local heat, such as heating pads, to the area of use, nor should they use it in conjunction with a medicated patch. It is also important to advise patients to avoid contact with eyes or mucous membranes and to refrain from using this product simultaneously with other topical analgesics.

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 necessary beyond standard storage practices.

Additional Clinical Information

Patients aged 12 years and older are advised to apply the medication to the affected area no more than 3 to 4 times daily. For children under 12 years of age, consultation with a healthcare professional is recommended prior to use.

Clinicians should counsel patients to seek advice from a health professional if they are pregnant or breastfeeding. Additionally, it is crucial to keep the product out of reach of children; in the event of ingestion, immediate medical assistance should be sought or contact with a Poison Control Center (1-800-222-1222) is recommended.

Drug Information (PDF)

This file contains official product information for Meijer Pain Relieving Max Strength with Lavender Essential Oil, 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 Pain Relieving Max Strength with Lavender Essential Oil, 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.