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Kroger Analgesic

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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)
Marketed in the U.S.
Since 2019
Label revision date
February 22, 2024
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
Marketed in the U.S.
Since 2019
Label revision date
February 22, 2024
Manufacturer
THE KROGER CO
Registration number
M017
NDC root
30142-260

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 HCl 4% is a fast-acting analgesic cream designed to provide temporary relief from pain. This non-greasy and fragrance-free cream is formulated to help soothe discomfort effectively. It contains the same active ingredient found in ASPERCREME® with Lidocaine, making it a maximum strength option for those seeking pain relief.

You can use Lidocaine HCl 4% to target areas of pain, allowing you to manage discomfort in a convenient and easy-to-apply form.

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. There are no known teratogenic effects (which means it does not cause birth defects) or nonteratogenic effects associated with this medication. Always consult with your healthcare provider for personalized advice and to ensure this treatment is right for you.

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 of age, it’s important not to use this medication without first consulting a doctor. Always prioritize your health and safety by seeking professional advice when needed.

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 blisters, to ensure your safety and well-being.

Side Effects

When using this product, it's important to be aware of some precautions. This product is for external use only, so avoid contact with your eyes and do not apply it to wounds or damaged skin. It's also advised not to bandage tightly or use it with heating pads. If you are pregnant or nursing, consult a healthcare professional before use. Additionally, avoid using large amounts, especially on raw or blistered areas.

If your condition worsens, or if symptoms persist for more than 7 days or return shortly after improvement, 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 at 1-800-222-1222.

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. 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 contact your doctor. Keep this product out of reach of children. If swallowed, seek emergency medical help or contact a Poison Control Center at 1-800-222-1222 immediately.

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 on 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 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 regarding any medications or treatments 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 any medication, including this product. 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. Since older adults may have different health needs and responses to medications, you should always consult with a healthcare provider before starting any new medication. They can help determine the right dosage and monitor for any potential side effects, ensuring that the treatment is safe and effective for you or your loved one.

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 should be used if you have renal impairment (kidney issues).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your health situation. They can help determine the best course of action 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 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 further handling, consult the guidelines provided with your product.

Additional Information

For adults and children aged 12 years and older, you should apply the medication to the affected area no more than 3 to 4 times a day. 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 patient counseling.

FAQ

What is Lidocaine HCl 4%?

Lidocaine HCl 4% is a fast-acting, fragrance-free analgesic cream used for the temporary relief of pain.

How should I use Lidocaine HCl 4%?

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 HCl 4%?

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

What precautions should I take when using this product?

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

What should I do if my condition worsens?

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

What should I do if Lidocaine HCl 4% is swallowed?

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

Is there any information on drug interactions?

No drug interactions information is provided for Lidocaine HCl 4%.

How should I store Lidocaine HCl 4%?

Store Lidocaine HCl 4% at room temperature.

Packaging Info

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

Packaging configurations for Kroger Analgesic.
Details

Drug Information (PDF)

This file contains official product information for Kroger Analgesic, 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 or nonteratogenic effects associated with its use.

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 treatment options 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 irritation and adverse effects. Tight bandaging is not recommended as it may impede circulation and exacerbate skin reactions. The use of heating pads or other heating devices in conjunction with the product is contraindicated, as this may lead to increased absorption and potential toxicity. Additionally, the application of large quantities, particularly over raw surfaces or blistered areas, is not advised due to the risk of heightened irritation and systemic absorption.

Warnings and Precautions

This product is intended for external use only. Healthcare professionals should advise patients to avoid contact with the eyes and to refrain from applying the product to wounds or damaged skin. It is important to avoid tight bandaging of the area where the product is applied, as well as the use of heating pads or other heating devices in conjunction with this product.

Patients who are pregnant or nursing should seek the advice of a healthcare professional prior to using this product, as with any medication. Caution is advised against using large quantities, particularly over raw surfaces or blistered areas, to prevent adverse effects.

Patients should be instructed to discontinue use and consult a physician if their condition worsens, if symptoms persist for more than 7 days, or if symptoms resolve 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 the Poison Control Center (1-800-222-1222) should be contacted.

Side Effects

Patients using this product should be aware that it 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. Additionally, patients should not bandage the area tightly or use the product in conjunction with heating pads or other heating devices.

As with any medication, it is advisable for patients who are pregnant or nursing to seek the advice of a healthcare professional prior to use. The product should not be used in large quantities, particularly over raw surfaces or blistered areas.

Patients are instructed to stop 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.

It is crucial to keep this product out of reach of children. In the event of accidental ingestion, patients should seek medical help or contact a Poison Control Center immediately at 1-800-222-1222.

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 warranted at this time.

Packaging & NDC

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

Packaging configurations for Kroger Analgesic.
Details

Pediatric Use

Pediatric patients under 12 years of age should not use this medication without consulting a doctor. For adolescents and children aged 12 years and older, the recommended application is to the affected area no 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 nursing mothers are advised to seek the counsel of a healthcare professional prior to using this product. The safety of this medication during pregnancy has not been established, and potential risks to fetal outcomes should be carefully considered. It is essential for women of childbearing potential to discuss their individual circumstances with their healthcare provider to ensure informed decision-making regarding the use of this product during pregnancy and lactation.

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

Patients with renal impairment have not been specifically addressed in the drug insert 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 lack of data necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients, although specific recommendations are not provided.

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. Contacting a Poison Control Center at 1-800-222-1222 is recommended for guidance on appropriate actions to take.

It is essential to monitor for potential symptoms of overdosage, which may vary depending on the specific substance involved. Healthcare providers should be prepared to assess the patient's condition and provide necessary interventions based on the clinical presentation.

Management of overdosage may involve supportive care and symptomatic treatment. Healthcare professionals should ensure that the patient is stabilized and closely monitored throughout the treatment process.

Nonclinical Toxicology

As with any drug, it is advised that individuals who are pregnant or nursing seek the advice of a health professional before using this product. 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 available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children. 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.

Patients should be informed 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 cautioned to avoid contact with the eyes and not to apply it to wounds or damaged skin. They should also be advised against bandaging the area tightly and 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 healthcare 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 skin.

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

For adults and children aged 12 years and older, the medication should be applied to the affected area no more than 3 to 4 times daily. It is advised that children under 12 years of age should not use this medication without consulting a doctor. No further information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Kroger Analgesic, 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 Kroger Analgesic, 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.