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Meijer Pain Relief

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Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
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
December 20, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
Dosage form
Gel
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
December 20, 2024
Manufacturer
Meijer
Registration number
M017
NDC root
79481-1087
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

You can use this medication for the temporary relief of pain. It is designed to help alleviate discomfort, making it easier for you to manage your daily activities. If you have any specific questions about how it works or its uses, feel free to ask your healthcare provider for more information.

Uses

You can use this medication for the temporary relief of pain. Whether you're dealing with a headache, muscle ache, or any other type of discomfort, this medication can help ease your symptoms for a short period. Always remember to follow the recommended guidelines for use to ensure safety and effectiveness.

Dosage and Administration

Before using the product, make sure to clean the affected area thoroughly. For adults and children aged 12 years and older, you should apply the product to the affected area no more than 3 to 4 times a day. If the user is a child under 12 years old, it’s important to consult a doctor before use to ensure safety and proper guidance.

What to Avoid

It's important to be aware of specific instructions regarding the use of 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 potential harm.

Currently, there are no listed contraindications, controlled substance classifications, or concerns about abuse, misuse, or dependence associated with this medication. Always follow the guidance provided by your healthcare professional to ensure safe use.

Side Effects

When using this product, it's important to be aware of some potential side effects. You should stop using it and consult a doctor if your condition worsens, if symptoms last longer than 7 days, or if they improve and then return shortly after. Additionally, watch for any redness or irritation that may develop.

Please remember that this product is for external use only and is flammable, so avoid using it while smoking or near heat and flames. Be careful to keep it away from your eyes, and do not apply it to wounds or damaged skin. Avoid tightly bandaging the area where you apply the product.

Warnings and Precautions

This product is for external use only and is flammable, so please avoid using it while smoking or near any heat or flames. When applying, be careful to keep it away from your eyes, and do not use it on wounds or damaged skin. It's important not to bandage the area tightly.

If your condition worsens, if symptoms last longer than 7 days, or if they improve and then come back within a few days, you should stop using the product and consult your doctor. Additionally, if you experience any redness or irritation, please reach out to your healthcare provider.

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

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 concerned about a possible overdose, seek medical help right away.

In case of an overdose, contacting your local emergency services or going to the nearest hospital is crucial. Always keep the medication packaging with you, as it can help healthcare professionals understand what you've taken. Remember, it's better to be safe and get checked out if you have any doubts about your health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to know that the safety of this medication during pregnancy has not been established. Due to potential risks to the developing fetus, it is generally not recommended for use while you are pregnant. Always consult with your healthcare provider to discuss any medications you are considering and to ensure the best care for you and your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. This means that, based on current knowledge, you can use this product without concern for its effects on your milk production or your baby’s health.

Pediatric Use

If your child is under 12 years old, it's important to consult a doctor before using this medication. For those aged 12 and older, you can apply it to the affected area, but be sure not to exceed 3 to 4 applications per day. Always follow these guidelines to ensure safe and effective use for your child.

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, it’s important to consult with a healthcare provider for personalized advice. 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 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 usual recommendations for monitoring or safety considerations related to renal impairment (kidney issues) are not provided.

It's always best to discuss your individual situation with your healthcare provider, who can offer personalized advice and ensure that any medications you take are safe and effective for you.

Hepatic Impairment

If you have liver 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 apply, and there are no special monitoring requirements or precautions outlined for patients with liver impairment.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe for your liver health. They can provide guidance based on your individual situation and help monitor your liver function as needed.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no specific drug interactions or laboratory test interactions noted for your treatment. This ensures that your healthcare team can monitor your health effectively and make informed decisions about your care.

Always feel free to ask questions and share all the medications and supplements you are using. This helps to avoid any potential issues and ensures that you receive the best possible treatment tailored to your needs.

Storage and Handling

To ensure the best performance of your product, store it at room temperature and keep it away from direct light. It's important not to freeze the product, as this can affect its effectiveness. Always make sure the container is tightly closed when not in use to maintain its integrity. Once opened, please remember to discard the product after use to ensure safety and effectiveness.

Additional Information

You should use this product only on the skin and apply it to the affected area no more than 3 to 4 times a day if you are an adult or a child aged 12 years or older. If the user is under 12, consult a doctor first. Remember, this product is flammable, so avoid using it while smoking or near any heat sources.

Before applying, clean the affected area and be careful to avoid contact with your eyes. Do not apply it to wounds or damaged skin, and avoid wrapping the area tightly. If your condition worsens, symptoms last more than 7 days, or if you notice any redness or irritation, stop using the product and consult a doctor. If swallowed, seek medical help or contact a Poison Control Center immediately.

FAQ

What is the purpose of this drug?

This drug is used for the temporary relief of pain.

How should I apply this product?

Clean the affected area before applying the product. Adults and children 12 years and older should apply it to the affected area no more than 3 to 4 times daily. Children under 12 years old should ask a doctor.

Are there any warnings I should be aware of?

Yes, this product is for external use only and is flammable. Avoid contact with eyes, do not apply to wounds or damaged skin, and do not bandage tightly.

What should I do if I swallow this product?

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

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

Stop use and ask a doctor if your condition worsens, if symptoms persist for more than 7 days, or if redness or irritation develops.

Is this product safe to use during pregnancy?

Safety during pregnancy has not been established, and use is not recommended due to potential risks to the fetus.

Can nursing mothers use this product?

There are no specific warnings or recommendations regarding the use of this product by nursing mothers.

How should I store this product?

Store at room temperature, protect from light, do not freeze, and keep the container tightly closed. Discard after opening.

Packaging Info

Below are the non-prescription pack sizes of Meijer Pain Relief (lidocaine hcl 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Pain Relief.
Details

Drug Information (PDF)

This file contains official product information for Meijer Pain Relief, 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 text.

Uses and Indications

This drug is indicated for the temporary relief of pain. It is intended for use in patients experiencing acute pain conditions. Healthcare professionals should assess the appropriateness of this medication based on individual patient needs and the specific pain management requirements.

Dosage and Administration

The affected area should be cleaned thoroughly prior to the application of the product. For adults and children aged 12 years and older, the product may be applied to the affected area up to 3 to 4 times daily. For children under 12 years of age, it is recommended to consult a physician before use.

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

For external use only; this product is flammable and should not be used while smoking or near heat or flame. Healthcare professionals should advise patients to avoid contact with eyes and to refrain from applying the product to wounds or damaged skin. Additionally, it is important to avoid tight bandaging of the area where the product is applied.

Patients should be instructed 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. The development of redness or irritation at the application site also warrants cessation of use and consultation with a physician.

In the event of accidental ingestion, immediate medical assistance should be sought, or the local Poison Control Center should be contacted without delay.

Side Effects

Patients should be aware that this product is for external use only and is flammable; it should not be used while smoking or near heat or flame. When using this product, it is important to avoid contact with the eyes, refrain from applying it to wounds or damaged skin, and 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 occur again within a few days, patients are advised to stop use and consult a doctor. Additionally, if redness or irritation develops, it is recommended to discontinue use and seek medical advice.

Drug Interactions

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

Packaging & NDC

Below are the non-prescription pack sizes of Meijer Pain Relief (lidocaine hcl 4%). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Pain Relief.
Details

Pediatric Use

Pediatric patients under 12 years of age should consult a healthcare professional before use. 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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy, given the lack of targeted data for this population.

Pregnancy

Safety during pregnancy has not been established for this medication. Use is not recommended during pregnancy due to potential risks to the fetus. Healthcare professionals should consider alternative treatments for pregnant patients to avoid any adverse fetal outcomes. Women of childbearing potential should be counseled on the importance of effective contraception while using this medication.

Lactation

There are no specific warnings or recommendations regarding the use of this product by nursing mothers. Additionally, there is no information available concerning the potential for excretion in breast milk or any associated risks to breastfed infants during lactation.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing 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 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 established dosage adjustments, special monitoring requirements, or precautions 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 adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

If the substance involved is known, specific antidotes or treatments may be indicated, and healthcare professionals should refer to established guidelines for the management of overdose related to that particular substance.

In all cases, contacting a poison control center or a medical toxicologist for guidance is recommended to ensure appropriate management and intervention.

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 these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

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 includes specific NDC numbers, which should be referenced for accurate identification. It is essential to store the product at room temperature, ensuring that it is protected from light exposure. Freezing the product is strictly prohibited, as it may compromise its integrity. The container must be kept tightly closed to maintain the product's quality, and it is important to discard any remaining product after opening to ensure safety and efficacy.

Additional Clinical Information

Patients aged 12 years and older are advised to apply the topical product to the affected area no more than 3 to 4 times daily, while children under 12 should consult a doctor before use. Clinicians should counsel patients that the product is for external use only and is flammable; it should not be used while smoking or near heat or flame.

Patients should avoid contact with eyes, refrain from applying the product to wounds or damaged skin, and avoid tight bandaging. They are instructed to stop use and consult a doctor if the condition worsens, if symptoms persist for more than 7 days, or if redness or irritation develops. In the event of ingestion, immediate medical assistance or contact with a Poison Control Center is recommended. It is also important for patients to clean the affected area prior to application.

Drug Information (PDF)

This file contains official product information for Meijer Pain Relief, 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 Relief, 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.