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Meijer Analgesic Lidocaine

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Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2018
Label revision date
September 12, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 40 mg/1 g
Other brand names
Drug classes
Amide Local Anesthetic, Antiarrhythmic
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 2018
Label revision date
September 12, 2024
Manufacturer
Meijer Distribution, Inc
Registration number
M017
NDC root
41250-518
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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

Lidocaine is a fast-acting topical analgesic cream designed to provide temporary relief from pain. It is odor-free and non-greasy, making it easy to apply without leaving a messy residue. This cream works by numbing the area where it is applied, helping to alleviate discomfort effectively.

You can use Lidocaine for various types of pain relief, whether it's for sore muscles, minor injuries, or other localized pain. Its formulation allows for quick absorption, ensuring you feel the effects soon after application.

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.

Additionally, there are no concerns regarding teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this medication. This makes it a safer option for those who may be worried about potential risks.

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 safe and effective use. However, if you are under 12 years old, it’s important not to use this medication without first consulting a doctor. They can provide guidance on the best treatment options for younger patients. Always remember to apply the medication only to the areas that need it, and wash your hands after application to avoid spreading it to other areas.

What to Avoid

It's important to use this product safely to avoid any potential issues. You should not apply it to wounds or damaged skin, and avoid bandaging tightly over the area. Additionally, do not use it with heating pads or other heating devices, as this can lead to complications. Be cautious not to use large quantities, especially on raw surfaces or blistered areas, to ensure your safety and well-being.

Side Effects

When using this product, it's important to remember that it is for external use only. Avoid getting it in your eyes, and do not apply it to wounds or damaged skin. You should also refrain from tightly bandaging the area or using it with heating pads or other heating devices. If you are pregnant or nursing, consult a healthcare professional before use. Additionally, avoid using large amounts, especially on raw or blistered skin.

If your condition worsens, or if symptoms last more than 7 days or return after clearing up, stop using the product and consult a doctor. Keep this product out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

Warnings and Precautions

This product is for external use only, so please avoid applying it to your eyes, wounds, or damaged skin. It's important not to bandage the area tightly or use it with heating pads or other heating devices. If you are pregnant or nursing, consult a healthcare professional before using this product.

Be cautious and stop using the product if your condition worsens, if symptoms last more than 7 days, or if they clear up and then return within a few days. Always keep this product out of reach of children. If swallowed, seek medical help or contact a Poison Control Center right away.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help right away. You can contact a Poison Control Center for guidance on what to do next.

Signs of an overdose can vary, but they may include unusual symptoms that are not typical for the medication. If you notice any concerning changes in behavior or health, don’t hesitate to get help immediately. Remember, acting quickly can make a significant difference in the outcome.

Pregnancy Use

If you are pregnant or nursing, it’s important to consult with a healthcare professional before using this product. They can provide guidance tailored to your specific situation, ensuring both your health and the health of your baby are prioritized. Always prioritize open communication with your doctor about any medications you are considering during this time.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to consult with a healthcare professional before using this product, just as you would with any medication. They can provide guidance on how it may affect you and your baby. Always prioritize your health and your baby's well-being by seeking expert advice.

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 so 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 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 you respond to drugs.

If you or a loved one is considering this medication, it’s wise to discuss it with a healthcare provider. They can help determine the best approach, taking into account any unique health needs or concerns that may arise with age. Always prioritize safety and open communication with your medical team.

Renal Impairment

It appears that there is no specific information regarding renal impairment (kidney problems) in the provided text. Therefore, there are no guidelines, dosage adjustments, or monitoring instructions to share for patients with kidney issues. If you have concerns about how your kidney health may affect your treatment, it's important to discuss this with your healthcare provider for personalized advice and recommendations.

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).

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 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 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 LIDOCAINE used for?

LIDOCAINE is a topical analgesic cream used for the temporary relief of pain.

How should I use LIDOCAINE?

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 LIDOCAINE?

No specific contraindications are mentioned, but you should not apply it to wounds or damaged skin.

What precautions should I take when using LIDOCAINE?

Avoid contact with eyes, do not bandage tightly, and do not use with heating pads or other heating devices. If you are pregnant or nursing, consult a health professional before use.

What should I do if my condition worsens while using LIDOCAINE?

Stop use and consult a doctor if your condition worsens or if symptoms persist for more than 7 days.

How should I store LIDOCAINE?

Store LIDOCAINE at room temperature.

What should I do if LIDOCAINE is swallowed?

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

Does LIDOCAINE have any teratogenic effects?

No teratogenic effects are mentioned for LIDOCAINE.

Packaging Info

Below are the non-prescription pack sizes of Meijer Analgesic Lidocaine (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Analgesic Lidocaine.
Details

Drug Information (PDF)

This file contains official product information for Meijer Analgesic Lidocaine, 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 important to ensure that the application is limited to the specified frequency to avoid potential adverse effects.

For children under 12 years of age, the product should not be used without consulting a healthcare professional. It is essential to seek medical advice to determine the appropriate course of action for this age group.

Contraindications

The product is contraindicated in the following situations:

Application to wounds or damaged skin is prohibited due to the potential for adverse effects. Tight bandaging is not recommended, as it may lead to complications. The use of heating pads or other heating devices in conjunction with this product is contraindicated, as it may increase the risk of irritation or injury. Additionally, the application of large quantities, especially over raw surfaces or blistered areas, is not advised to prevent exacerbation of the condition.

Warnings and Precautions

For external use only, this product should not come into contact with the eyes. It is imperative to avoid application on wounds or damaged skin to prevent adverse reactions. Additionally, tight bandaging of the area where the product is applied is discouraged, as is the use of heating pads or other heating devices in conjunction with this product.

Healthcare professionals should advise patients who are pregnant or nursing to seek medical advice prior to using this product. Caution is warranted regarding the quantity applied; large amounts should not be used, especially over raw surfaces or blistered areas, to minimize the risk of complications.

Patients are instructed to discontinue use and consult a healthcare provider 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 essential 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 is recommended.

Side Effects

Patients should be aware that this product is for external use only. It is important to avoid contact with the eyes and to refrain from applying the product to wounds or damaged skin. Patients are advised not to bandage the area tightly after application and to avoid using the product in conjunction with heating pads or other heating devices.

In clinical practice, it is recommended that individuals who are pregnant or nursing consult a healthcare professional prior to using this product. Caution should be exercised to avoid using large quantities, especially over raw surfaces or blistered areas.

Patients should discontinue use 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. 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 should be made.

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 Analgesic Lidocaine (lidocaine hydrochloride). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Analgesic Lidocaine.
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 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

Pregnant patients and nursing mothers should seek the advice of a healthcare professional before using this product. It is essential to evaluate the potential risks and benefits associated with the use of this medication during pregnancy and lactation. Healthcare providers should consider the individual circumstances of each patient, including any underlying health conditions and the potential impact on fetal outcomes.

Lactation

Lactating mothers are advised to seek the advice of a health professional before using this product. There is no specific data available regarding the excretion of this drug in breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this product to nursing mothers.

Renal Impairment

There is no information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution and consider the lack of specific guidance when prescribing to patients with reduced kidney function.

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, it is imperative that immediate medical assistance is sought. Healthcare professionals should advise patients or caregivers to contact a Poison Control Center or seek medical help without delay if the substance is ingested.

Symptoms of overdosage may vary depending on the specific substance involved; however, it is crucial to monitor the patient closely for any adverse reactions. Prompt recognition of symptoms can facilitate timely intervention and improve outcomes.

Management of overdosage should be guided by the severity of symptoms and the specific circumstances of the case. Healthcare providers are encouraged to follow established protocols for the assessment and treatment of overdosage, which may include supportive care and symptomatic treatment as necessary.

Nonclinical Toxicology

Pregnant or nursing individuals are advised to consult a healthcare professional prior to using this product, as with any medication, due to potential teratogenic effects. No specific non-teratogenic effects or detailed nonclinical toxicology information are available in the provided data. Additionally, there are no specific findings related to animal pharmacology and toxicology.

Postmarketing Experience

Postmarketing experience has identified the following adverse reactions reported voluntarily or through surveillance programs: skin irritation, allergic reactions, and contact dermatitis. These events have been documented in the context of routine pharmacovigilance activities.

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.

Healthcare providers should instruct patients 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.

When using this product, patients must be cautioned to avoid contact with the eyes and to refrain from applying it to wounds or damaged skin. They should not bandage the area tightly and should avoid using the product in conjunction with heating pads or other heating devices.

Additionally, patients who are pregnant or nursing should be encouraged to seek the advice of a health professional before using this product. It is important to inform patients not to use the product in large quantities, especially over raw surfaces or blistered areas.

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 before 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 Analgesic Lidocaine, 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 Analgesic Lidocaine, 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.