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Walgreens Pain Relieving with Lavender

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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 2022
Label revision date
October 31, 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 2022
Label revision date
October 31, 2024
Manufacturer
Walgreen Company
Registration number
M017
NDC root
0363-1225
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

Lidocaine HCl 4% is a topical analgesic, which means it is a pain-relieving liquid that you can apply directly to your skin. This product is designed for the temporary relief of pain and works quickly to help alleviate discomfort. It features a no-mess applicator, making it easy for you to apply it to the affected area without any hassle. Additionally, it contains lavender essential oil, which adds a soothing scent to the experience.

This maximum strength formulation is similar to the active ingredient found in Aspercreme, providing effective pain relief in a convenient 2.5 FL OZ (73mL) bottle.

Uses

You can use this medication for the temporary relief of pain. It is designed to help alleviate discomfort for a short period, making it useful when you need quick relief.

Rest assured, there are no teratogenic effects (which means it does not cause birth defects) associated with this medication, so it is considered safe in that regard.

Dosage and Administration

If you are 12 years old or older, you can apply the medication to the affected area up to 3 to 4 times a day. Make sure to follow this guideline to ensure the best results. If you are caring for a child under 12, it’s important to consult a doctor before using this medication, as they can provide specific advice tailored to your child's needs. Always remember to apply the medication only to the areas that need treatment.

What to Avoid

You should avoid applying this medication over large areas of your body or on any cut, irritated, or swollen skin, including puncture wounds. It's important not to bandage the area or use local heat, such as heating pads, while using this medication, and you should never combine it with other topical pain relievers. Additionally, be careful to keep it away from your eyes and mucous membranes to prevent irritation. Following these guidelines will help ensure your safety and the effectiveness of the treatment.

Side Effects

When using this product, it's important to be aware of certain precautions and potential side effects. You should only apply it to small areas of unbroken skin and avoid using it on cuts, irritated, or swollen skin, as well as puncture wounds. Make sure to keep it away from your eyes and mucous membranes, and do not use it alongside other topical pain relievers. If you notice any redness or irritation, or if your condition worsens or does not improve after 7 days, you should stop using the product and consult a doctor.

In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately at 1-800-222-1222. Always remember that this product is for external use only.

Warnings and Precautions

This product is for external use only, so be sure to follow all directions and warnings on the packaging carefully. Avoid applying it to large areas of your body, and do not use it on cut, irritated, or swollen skin, including puncture wounds. It's important not to bandage the area or apply heat, such as heating pads, while using this product. Also, keep it away from your eyes and mucous membranes, and do not use it alongside other topical pain relievers.

If your condition worsens, symptoms last more than 7 days, or if they clear up and return within a few days, stop using the product and consult your doctor. You should also discontinue use and seek medical advice if you notice any redness or irritation. Keep this product out of reach of children, and if swallowed, contact a Poison Control Center at 1-800-222-1222 or seek medical help immediately. Lastly, remember that this product is flammable, so keep it away from fire or flames.

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 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 receive personalized advice that considers your health and the well-being of your baby. Always prioritize open communication with your doctor to make informed decisions about your care during this time.

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 in a 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 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 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 (issues with liver function).

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver health and medication use. They can help ensure that you receive the safest and most effective treatment based on your individual needs.

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 it in a clean environment to ensure it remains safe for use. If you have any questions about disposal or other safety measures, 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 a day if you are an adult or a child aged 12 years and 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 LIDOCAINE HCl 4%?

LIDOCAINE HCl 4% is a topical analgesic (pain reliever) with lavender essential oil, designed for the temporary relief of pain.

How do I use LIDOCAINE HCl 4%?

Apply to the affected area not more than 3 to 4 times daily for adults and children 12 years and older. For children under 12, consult a doctor.

Are there any contraindications for using this product?

Do not apply over large areas of the body, on cut or irritated skin, or use with bandages or heating pads. Avoid contact with eyes and mucous membranes.

What should I do if I experience side effects?

Discontinue use and consult a doctor if your condition worsens, symptoms persist for more than 7 days, or if you notice redness or irritation.

Is LIDOCAINE HCl 4% safe to use during pregnancy or breastfeeding?

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

What should I do if I accidentally swallow LIDOCAINE HCl 4%?

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

How should I store LIDOCAINE HCl 4%?

Store at room temperature.

Packaging Info

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

Packaging configurations for Walgreens Pain Relieving with Lavender.
Details

Drug Information (PDF)

This file contains official product information for Walgreens Pain Relieving with Lavender, 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. It is specifically designed to provide short-term alleviation of discomfort associated with various conditions.

Limitations of Use: There are no noted teratogenic or nonteratogenic effects associated with this drug. Therefore, it may be considered for use in populations where such concerns are relevant, although healthcare professionals should always evaluate the individual patient's circumstances.

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, it is advised to consult a healthcare professional prior to use to determine the appropriate course of action.

Contraindications

Use of this product is contraindicated in the following situations:

Application over large areas of the body is prohibited due to the potential for systemic absorption and adverse effects. The product should not be applied to cut, irritated, or swollen skin, nor on puncture wounds, as this may exacerbate irritation or lead to infection.

Bandaging or the application of local heat, such as heating pads, to the area of use is contraindicated, as it may increase absorption and the risk of adverse reactions. Contact with eyes or mucous membranes must be avoided to prevent irritation or injury.

Concurrent use with other topical analgesics is not recommended, as this may increase the risk of systemic toxicity or local irritation.

Warnings and Precautions

For external use only, this product must be utilized strictly as directed. Healthcare professionals should advise patients to read and adhere to all instructions and warnings provided on the carton to ensure safe application.

It is imperative that the product not be applied over large areas of the body. Additionally, it should not be used on cut, irritated, or swollen skin, nor on puncture wounds. The application of bandages or the use of local heat sources, such as heating pads, is contraindicated in conjunction with this product. Furthermore, it should not be used simultaneously with other topical analgesics to avoid potential adverse effects.

Healthcare providers should instruct patients to avoid contact with the eyes and mucous membranes. In the event that the condition worsens, or if symptoms persist for more than 7 days, or if symptoms resolve and then recur within a few days, patients should discontinue use and seek medical advice. The presence of redness or the development of irritation also necessitates discontinuation of use and consultation with a healthcare professional.

This product must be kept out of reach of children. In cases of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center (1-800-222-1222) should be contacted without delay.

Due to its flammable nature, it is essential to keep this product away from fire or flame to prevent any hazardous incidents.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is important to avoid applying the product over large areas of the body and to refrain from using it on cut, irritated, or swollen skin, as well as on puncture wounds. Additionally, patients should not bandage the area of application or apply local heat, such as heating pads, nor should they use it concurrently with other topical analgesics. Contact with eyes or mucous membranes must be avoided.

In the event that the condition worsens, symptoms persist for more than 7 days, or if symptoms clear up and then recur within a few days, patients are advised to discontinue use and consult a healthcare professional. The presence of redness or the development of irritation also necessitates discontinuation and medical consultation.

In cases of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted 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 necessary at this time.

Packaging & NDC

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

Packaging configurations for Walgreens Pain Relieving with Lavender.
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

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 potential adverse effects or changes in efficacy, 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 currently no available data regarding the excretion of this drug in human 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 no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the drug insert. Therefore, healthcare professionals should exercise caution when prescribing this medication to individuals with reduced kidney function, as the lack of data may impact the drug's efficacy and safety profile in this population. Regular monitoring of renal function is advisable to ensure patient safety.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this medication. Consequently, there are no 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 available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep the medication 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 use the medication only as directed and to read and follow all directions and warnings provided on the carton. It is important to emphasize that the product should not be applied over large areas of the body and should not be used on cut, irritated, or swollen skin, nor on puncture wounds.

Healthcare providers should counsel patients against bandaging or applying local heat, such as heating pads, to the area of use, and to avoid using the product in conjunction with a medicated patch. Additionally, patients should be warned to prevent contact with eyes or mucous membranes.

Patients should be advised not to use the medication simultaneously with other topical analgesics. They should be instructed to 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. Furthermore, patients should be informed to stop using the product and seek medical advice if they experience redness or if irritation develops.

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

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 important to keep the product out of reach of children; in the event of ingestion, medical assistance should be sought immediately or contact a Poison Control Center at 1-800-222-1222.

Drug Information (PDF)

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