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Walgreens Pain Relieving Cream

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Active ingredient
Lidocaine Hydrochloride 4 g/100 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 2022
Label revision date
October 31, 2023
Active ingredient
Lidocaine Hydrochloride 4 g/100 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 2022
Label revision date
October 31, 2023
Manufacturer
Walgreens
Registration number
M017
NDC root
0363-3037

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Drug Overview

This medication is designed to temporarily relieve minor joint and muscle pain. It can be a helpful option if you're experiencing discomfort in these areas, providing you with some relief when you need it most.

Uses

If you're dealing with minor joint and muscle pain, this medication can help provide temporary relief. It's designed to ease discomfort, allowing you to go about your daily activities with less pain. Whether it's from exercise, strain, or other minor injuries, you can count on this treatment to help soothe those aches.

Dosage and Administration

To use this medication effectively, you should apply a thin layer to the affected area of your skin every 6 to 8 hours. It's important not to exceed three applications within a 24-hour period. If you are treating a child under 12 years old, please consult a doctor for guidance on the appropriate use.

Make sure to follow these instructions closely to ensure the best results. If you have any questions or concerns about how to apply the medication, don’t hesitate to reach out to a healthcare professional for assistance.

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 any cut, irritated, or swollen skin. Additionally, avoid using it on punctured wounds. If you find that you need to use it for more than one week, please consult your doctor first.

Make sure to keep it away from your eyes, and do not cover the treated area with a bandage or apply heat. Lastly, avoid using this medication alongside other topical pain relievers to prevent any adverse effects. Your safety is a priority, so following these guidelines is essential.

Side Effects

When using this product, it's important to be aware of potential side effects. If you notice that your condition worsens, experience redness, or develop irritation, you should stop using the product. Additionally, if your symptoms last more than seven days or improve only to return shortly after, it's advisable to discontinue use.

Remember, this product is for external use only. Always monitor your skin's response and consult a healthcare professional if you have concerns about any reactions.

Warnings and Precautions

This product is for external use only, so please keep it out of reach of children and pets. If someone accidentally swallows it, seek medical help or contact a Poison Control Center immediately. Avoid using it on large areas of the body, on cut, irritated, or swollen skin, and do not apply it to punctured wounds. It's important not to use this product for more than one week without consulting your doctor.

If your condition worsens, if you notice redness, or if irritation develops, stop using the product and call your doctor. Additionally, if your symptoms persist for more than seven days or improve and then return within a few days, you should also stop use and reach out to your healthcare provider.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While the specific signs of an overdose are not detailed, common symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, or if you are unsure, seek medical help right away.

In case of an overdose, contact your local emergency services or go to the nearest hospital. It's crucial to provide them with as much information as possible about the substance taken and the amount, if known. Remember, acting quickly can make a significant difference in your health and safety.

Pregnancy Use

If you are pregnant or planning to become pregnant, it’s important to consult with a healthcare professional before using this medication. They can provide guidance tailored to your specific situation and help you understand any potential risks. Always prioritize your health and the health of your baby by seeking expert advice.

Lactation Use

If you are breastfeeding, it's important to talk to your healthcare professional before using this product. There is a possibility that it can be passed into your breast milk, and the effects on your nursing infant have not been thoroughly studied. Therefore, exercising caution is recommended to ensure the safety and well-being of both you and your baby.

Pediatric Use

When using this medication for children, it's important to follow specific guidelines. For adults and children over 12 years old, you can apply a thin layer to the affected area every 6 to 8 hours, but make sure not to exceed three applications in a 24-hour period.

If your child is under 12 years of age, you should consult a doctor before using this medication. This ensures that you receive the appropriate advice and dosage for their specific needs. Always prioritize your child's safety and well-being by seeking professional guidance.

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 before starting the medication. 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 appropriate for your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help monitor your liver function and make any necessary adjustments to your care.

Drug Interactions

It's important to be cautious when using this medication. You should not use it at the same time as other topical analgesics (pain-relieving creams or gels applied to the skin). Mixing these products can increase the risk of side effects or reduce their effectiveness.

Always discuss any medications you are taking with your healthcare provider. They can help ensure that your treatment is safe and effective, taking into account all the products you may be using.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature. It's important to keep it out of reach of children and pets to prevent any accidental ingestion or misuse. Once you open the product, be sure to discard it after use to maintain safety and hygiene. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should apply a thin layer of the medication to the affected area every 6 to 8 hours, but do not exceed three applications in a 24-hour period if you are an adult or a child over 12 years old. For children under 12, consult a doctor before use. Always use the product as directed by reading and following all instructions and warnings on the packaging.

Be careful to avoid contact with your eyes, and do not cover the treated area with bandages or apply heat. It's important not to use this medication alongside other topical pain relievers. If your condition worsens, if you notice redness or irritation, or if symptoms last more than 7 days or return after clearing up, seek advice from a healthcare professional. Keep the product out of reach of children and pets, and if ingested, contact a medical professional or Poison Control Center immediately.

FAQ

What does this drug do?

This drug temporarily relieves minor joint and muscle pain.

How should I apply this drug?

For adults and children over 12 years, apply a thin layer to the affected area every 6 to 8 hours, not exceeding 3 applications in a 24-hour period.

What should I do if I experience side effects?

Stop use if the condition worsens, redness is present, or irritation develops. If symptoms persist for more than 7 days or return after clearing up, consult a healthcare professional.

Are there any precautions I should take?

Do not use on large areas of the body, on cut or irritated skin, or at the same time as other topical analgesics. Avoid contact with eyes.

Can children use this drug?

Children under 12 years of age should ask a doctor before use.

What should I do if I swallow this drug?

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

How should I store this drug?

Store at room temperature and keep out of reach of children and pets. Discard after opening.

Is this drug safe to use during pregnancy or while nursing?

Consult a healthcare professional before use if you are pregnant or nursing, as there is potential for excretion in breast milk.

Packaging Info

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

Packaging configurations for Walgreens Pain Relieving Cream.
Details

Drug Information (PDF)

This file contains official product information for Walgreens Pain Relieving Cream, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

No specific information related to the Description section for SPL code 34089-3 is provided in the text.

Uses and Indications

This drug is indicated for the temporary relief of minor joint and muscle pain. It is intended for use in patients experiencing discomfort due to various conditions affecting the musculoskeletal system.

Dosage and Administration

Adults and children over 12 years of age should apply a thin layer of the medication to the affected area every 6 to 8 hours. The total number of applications must not exceed 3 in a 24-hour period. For children under 12 years of age, it is advised to consult a physician before use.

The medication should be applied topically, ensuring that the affected area is clean and dry prior to application.

Contraindications

Use is contraindicated in the following situations:

  • Application on large areas of the body or on cut, irritated, or swollen skin due to the potential for increased absorption and adverse effects.

  • Application on punctured wounds, as this may lead to complications or delayed healing.

  • Use for more than one week without consulting a healthcare professional, to avoid potential misuse or adverse reactions.

  • Contact with eyes should be strictly avoided to prevent irritation or injury.

  • Bandaging or applying local heat to the area of use is contraindicated, as this may enhance absorption and increase the risk of systemic effects.

  • Concurrent use with other topical analgesics is not recommended, as this may lead to additive effects and increased risk of side effects.

Warnings and Precautions

For external use only. It is imperative that this product is kept out of reach of children and pets to prevent accidental ingestion or misuse. In the event of ingestion, immediate medical assistance should be sought, or contact a Poison Control Center without delay.

General precautions must be observed when using this product. It should not be applied to large areas of the body, nor should it be used on cut, irritated, or swollen skin. Additionally, the product is contraindicated for use on punctured wounds. Prolonged use beyond one week is not recommended without prior consultation with a healthcare professional.

Healthcare providers should advise patients to discontinue use and seek medical attention if the condition worsens, if redness occurs, or if irritation develops. Furthermore, if symptoms persist for more than seven days or if they resolve and then recur within a few days, patients should be instructed to stop using the product and consult their doctor.

In cases of accidental ingestion, it is crucial to obtain emergency medical help or contact a Poison Control Center immediately.

Side Effects

Patients using this product should be aware that it is intended for external use only. In clinical practice, adverse reactions may occur, and it is important to monitor for specific signs and symptoms.

Common adverse reactions include worsening of the condition being treated, the presence of redness, and the development of irritation. If any of these symptoms occur, patients are advised to discontinue use of the product.

Additionally, if symptoms persist for more than 7 days, or if they clear up and then recur within a few days, patients should stop using the product and consult a healthcare professional. These recommendations are based on clinical observations and are intended to ensure patient safety and effective management of their condition.

Drug Interactions

Concurrent use of this medication with other topical analgesics is contraindicated. The combination may increase the risk of adverse effects without providing additional therapeutic benefit. It is advised to avoid using multiple topical analgesics simultaneously to ensure patient safety and optimal therapeutic outcomes. Monitoring for any signs of increased local irritation or systemic effects is recommended if such combinations are inadvertently used.

Packaging & NDC

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

Packaging configurations for Walgreens Pain Relieving Cream.
Details

Pediatric Use

Pediatric patients over 12 years of age may apply a thin layer of the medication to the affected area every 6 to 8 hours, with a maximum of 3 applications within a 24-hour period. For children under 12 years of age, it is advised to consult a doctor before use.

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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in this population.

Pregnancy

Pregnant patients should consult a healthcare professional before using this medication. The safety of this drug during pregnancy has not been established, and potential risks to fetal outcomes are not fully understood. It is essential for women of childbearing potential to discuss their individual circumstances with their healthcare provider to weigh the benefits and risks associated with the use of this medication during pregnancy.

Lactation

Lactating mothers should consult a healthcare professional before using this product. There is a potential for excretion in breast milk. The effects on a nursing infant are not well studied; therefore, caution is advised.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available data 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 information necessitates careful clinical judgment and monitoring.

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 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 available information.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution and consider general principles of management for suspected cases of drug overdosage.

Recommended Actions In the event of an overdosage, it is essential to assess the patient's clinical status promptly. Healthcare providers should initiate supportive care and monitor vital signs closely. The management of overdosage may include the following steps:

  1. Assessment: Evaluate the patient's symptoms and history of exposure to the drug.

  2. Supportive Care: Provide symptomatic treatment as necessary, which may include intravenous fluids, oxygen supplementation, or other interventions based on the patient's condition.

  3. Consultation: Engage with a poison control center or a medical toxicologist for guidance on specific management strategies tailored to the drug involved.

Potential Symptoms While specific symptoms of overdosage are not detailed, healthcare professionals should remain vigilant for signs of toxicity that may arise from excessive dosing of medications. Symptoms can vary widely depending on the pharmacological properties of the drug and may include:

  • Altered mental status

  • Respiratory distress

  • Cardiovascular instability

  • Gastrointestinal disturbances

Management Procedures In cases of suspected overdosage, healthcare professionals should follow established protocols for decontamination, which may include activated charcoal administration if appropriate and within the recommended time frame post-ingestion. Continuous monitoring and supportive care are critical components of effective management.

In summary, while specific overdosage information is not available, healthcare professionals should prioritize patient safety through careful assessment, supportive care, and consultation with specialists as needed.

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 to keep the medication out of reach of children and pets to prevent accidental ingestion. Instruct patients that if the medication is swallowed, they should seek medical help or contact a Poison Control Center immediately.

It is essential for patients to use the medication only as directed. They should be encouraged to read and follow all directions and warnings provided on the carton to ensure safe and effective use.

Healthcare providers should also inform patients to avoid contact with the eyes, as this could lead to irritation or injury. Additionally, patients should be cautioned against bandaging or applying local heat to the area of use, as this may increase the risk of adverse effects.

Finally, it is important to advise patients not to use this medication simultaneously with other topical analgesics, as this could lead to increased side effects or diminished effectiveness.

Storage and Handling

The product is supplied in a configuration that ensures optimal usability. It is essential to store the product at room temperature to maintain its integrity and effectiveness. To ensure safety, the product should be kept out of reach of children and pets. Additionally, it is important to discard the product after opening to prevent any potential contamination or degradation.

Additional Clinical Information

Patients should apply a thin layer of the product to the affected area every 6 to 8 hours, with a maximum of three applications within a 24-hour period for adults and children over 12 years. For children under 12 years, it is advised to consult a doctor before use.

Clinicians should counsel patients to use the product only as directed, adhering to all instructions and warnings on the packaging. It is important to avoid contact with the eyes, refrain from bandaging or applying local heat to the treated area, and not to use the product concurrently with other topical analgesics. Patients should seek medical advice if their condition worsens, if redness or irritation occurs, or if symptoms persist beyond 7 days or recur shortly after resolution. Additionally, the product should be kept out of reach of children and pets, and immediate medical assistance should be sought if ingested.

Drug Information (PDF)

This file contains official product information for Walgreens Pain Relieving Cream, 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 Walgreens Pain Relieving Cream, 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.

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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.