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Aspercreme Lidocaine No-Mess Plus Lavender

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Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2020
Label revision date
October 25, 2023
Active ingredient
Lidocaine Hydrochloride 4 g/100 mL
Other brand names
Dosage form
Liquid
Route
Topical
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2020
Label revision date
October 25, 2023
Manufacturer
Chattem, Inc.
Registration number
M017
NDC root
41167-0568

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Drug Overview

Aspercreme is a pain relief liquid that contains 4% lidocaine (a local anesthetic that helps numb the skin) and lavender essential oil. It is designed to temporarily relieve minor pain, making it a helpful option for those seeking quick comfort from discomfort.

This product is available in a maximum strength formula and comes in a 2.5 fluid ounce (73 mL) bottle, providing you with a convenient way to manage minor aches and pains.

Uses

You can use this medication to temporarily relieve minor pain. It’s designed to help you feel more comfortable when dealing with everyday aches and discomforts. Rest assured, there are no known teratogenic effects (which means it doesn’t cause birth defects) associated with this medication, making it a safer option for those who may be concerned about such risks.

Dosage and Administration

If you are an adult or a child over 12 years old, you should apply a thin layer of the medication to the affected area every 6 to 8 hours. However, make sure not to exceed more than 3 applications within a 24-hour period.

For children who are 12 years old or younger, it’s important to consult a doctor before using this medication. This ensures that the treatment is safe and appropriate for their specific needs. Always follow these guidelines to help manage your condition effectively.

What to Avoid

You should avoid using this medication on large areas of your body or on any cut, irritated, or swollen skin. It's also important not to apply it to puncture wounds and to limit use to no more than one week without consulting your doctor.

Additionally, make sure to keep the medication away from your eyes and mucous membranes. Do not cover the treated area with a bandage, apply local heat (like heating pads), or use it alongside other topical pain relievers. 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 potential side effects and safety precautions. You should only apply it to small areas of unbroken skin and avoid using it on cuts, irritated skin, or puncture wounds. If you notice any redness, irritation, or if your condition worsens, stop using the product and consult a doctor. Additionally, if symptoms persist for more than a week or return shortly after improvement, seek medical advice.

Please remember that this product is flammable, so keep it away from fire or flames. Avoid contact with your eyes and mucous membranes, and do not use it alongside other topical pain relievers. For your safety, do not bandage the area or apply heat while using this product.

Warnings and Precautions

This product is for external use only, so please avoid applying it to large areas of your body or on any cut, irritated, or swollen skin. It should not be used on puncture wounds, and you should not use it for more than one week without consulting your doctor. Always follow the directions on the packaging carefully, and avoid contact with your eyes and mucous membranes. Do not apply heat or bandage the area where you use this product, and refrain from using it alongside other topical pain relievers.

If you notice that your condition worsens, if you see redness or irritation, or if your symptoms last longer than seven days or return shortly after improvement, stop using the product and consult your doctor. Remember, this product is flammable, so keep it away from fire or flames. Also, keep it out of reach of children; if swallowed, seek medical help or contact a Poison Control Center immediately.

Overdose

If you or someone else has swallowed too much of a medication, it’s important to seek medical help immediately. You can do this by contacting a Poison Control Center or going to the nearest emergency room. Acting quickly can make a significant difference in the outcome.

Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, don’t hesitate to get help right away. Remember, it’s always better to be safe and seek assistance if you suspect an overdose.

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 understand any potential risks and can make informed decisions about your health and the health of your baby. Always prioritize open communication with your doctor regarding your breastfeeding journey.

Pediatric Use

If your child is 12 years old or younger, it's important to consult with a doctor before using this medication. For those over 12, you can apply a thin layer to the affected area every 6 to 8 hours, but be sure not to exceed three applications in a 24-hour period.

Always keep this medication out of reach of children. If your child accidentally swallows it, seek medical help or contact a Poison Control Center immediately.

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 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 may affect you if your kidneys are not functioning properly.

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your kidney health. They can help monitor your condition and make any necessary adjustments to your treatment plan.

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).

Always consult your healthcare provider for personalized advice and to ensure that any medication you take is safe and appropriate for your liver health. They can help you understand how to manage your treatment effectively.

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 full list of medications and any health concerns during your appointments to receive the best care possible.

Storage and Handling

To ensure the safety and effectiveness of your product, store it at room temperature, away from any fire or flame. After each use, make sure to close the cap tightly to prevent any leaks or contamination. It's also important to keep the carton, as it contains essential information you may need later. The product comes in child-resistant packaging, which adds an extra layer of safety, especially if there are children around.

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. If the patient is 12 years old or younger, consult a doctor before use.

If you are pregnant or breastfeeding, it's important to ask a health professional before using this medication. Always keep it out of reach of children, and if swallowed, seek medical help or contact a Poison Control Center immediately.

FAQ

What is Aspercreme used for?

Aspercreme is used to temporarily relieve minor pain.

How should I apply Aspercreme?

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.

Can children use Aspercreme?

Children 12 years or younger should ask a doctor before use.

Are there any contraindications for using Aspercreme?

Do not use Aspercreme on large areas of the body, on cut or irritated skin, or for more than one week without consulting a doctor.

What precautions should I take when using Aspercreme?

Avoid contact with eyes and mucous membranes, do not bandage or apply local heat to the area, and do not use with other topical analgesics.

What should I do if I experience side effects?

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

Is Aspercreme safe to use during pregnancy or breastfeeding?

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

How should I store Aspercreme?

Store Aspercreme at room temperature, keep away from fire or flame, and ensure the cap is tightly closed after use.

What should I do if Aspercreme is swallowed?

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

Packaging Info

Below are the non-prescription pack sizes of Aspercreme Lidocaine No-Mess Plus Lavender (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aspercreme Lidocaine No-Mess Plus Lavender.
Details

Drug Information (PDF)

This file contains official product information for Aspercreme Lidocaine No-Mess Plus 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 minor pain.

There are no teratogenic effects associated with this drug. Additionally, no nonteratogenic effects have been reported.

Dosage and Administration

For adults and children over 12 years of age, a thin layer of the medication should be applied to the affected area every 6 to 8 hours. The total number of applications must not exceed 3 times within a 24-hour period.

For children 12 years of age or younger, it is recommended to consult a physician before use.

Contraindications

Use is contraindicated in the following situations:

Application on large areas of the body, or on cut, irritated, or swollen skin is prohibited due to the potential for increased absorption and adverse effects. The product should not be applied to puncture wounds, as this may lead to complications or infection.

Prolonged use beyond one week without consulting a healthcare professional is contraindicated to prevent potential adverse reactions.

Contact with the eyes and mucous membranes must be avoided to prevent irritation or injury. Additionally, the product should not be bandaged or subjected to local heat, such as heating pads or medicated patches, as this may enhance absorption and increase the risk of side effects. Concurrent use with other topical analgesics is also contraindicated to avoid additive effects and potential toxicity.

Warnings and Precautions

For external use only. This product should not be applied to large areas of the body, nor should it be used on cut, irritated, or swollen skin. It is contraindicated for application on puncture wounds and should not be used for more than one week without consulting a healthcare professional.

When utilizing this product, it is imperative to adhere strictly to the provided directions. Users must read and follow all instructions and warnings on the packaging. Care should be taken to avoid contact with the eyes and mucous membranes. Additionally, the area of application should not be bandaged, nor should local heat sources, such as heating pads or medicated patches, be applied concurrently. The use of other topical analgesics at the same time is also contraindicated.

Users are advised to discontinue use and consult a physician if any of the following occur: worsening of the condition, presence of redness, development of irritation, persistence of symptoms beyond 7 days, or if symptoms resolve and then recur within a few days. This product is flammable; therefore, it should be kept away from fire or flame.

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 should be made without delay.

Side Effects

Patients using this product should be aware of several important safety warnings and potential adverse reactions. This product is intended for external use only and should not be applied to large areas of the body, on cut, irritated, or swollen skin, or on puncture wounds. It is advised that patients do not use the product for more than one week without consulting a healthcare professional.

During use, patients must avoid contact with the eyes and mucous membranes. Additionally, it is important not to bandage the area of application, apply local heat (such as heating pads), or use the product concurrently with other topical analgesics.

Patients are instructed to discontinue use and consult a doctor if any of the following occur: worsening of the condition, presence of redness, development of irritation, or if symptoms persist for more than seven days or resolve and then recur within a few days.

Furthermore, the product is flammable; therefore, it should be kept away from fire or flame to prevent any hazardous incidents.

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 Aspercreme Lidocaine No-Mess Plus Lavender (lidocaine hcl). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Aspercreme Lidocaine No-Mess Plus Lavender.
Details

Pediatric Use

Pediatric patients 12 years of age or younger should consult a healthcare professional before use. For patients over 12 years, the recommended application is a thin layer to the affected area every 6 to 8 hours, with a maximum of 3 applications within a 24-hour period.

It is essential to keep this medication out of reach of children. In the event of accidental ingestion, immediate medical assistance should be sought, or contact a Poison Control Center.

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

Pregnant patients and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully considered in these populations to ensure the safety of both the mother and the fetus or infant.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is no specific data available regarding the excretion of this medication in 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 necessitates careful clinical judgment.

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 or contact a Poison Control Center without delay.

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 resolution of any complications arising from the overdosage.

Nonclinical Toxicology

If pregnant or breastfeeding, it is advised to consult a health professional prior to use. No non-teratogenic effects have been provided in the insert. Additionally, there is no information available regarding nonclinical toxicology or animal pharmacology and toxicology in the insert.

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.

Patients should be informed not to use the product on large areas of the body or on cut, irritated, or swollen skin, and it should not be applied to puncture wounds. It is important to counsel patients against using the product for more than one week without consulting a doctor.

Patients should be instructed to stop using the product and consult a doctor if their condition worsens, if redness is present, if irritation develops, or if symptoms persist for more than 7 days or clear up and then occur again within a few days.

Additionally, patients should be made aware that the product is flammable and should be kept away from fire or flame. When using this product, patients must use it only as directed and should read and follow all directions and warnings on the carton.

Healthcare providers should emphasize that patients should avoid contact with the eyes and mucous membranes while using the product. They should also advise against bandaging or applying local heat, such as heating pads or medicated patches, to the area of use. Furthermore, patients should be cautioned not to use this product simultaneously with other topical analgesics.

Storage and Handling

The product is supplied in child-resistant packaging, ensuring safety during storage and handling. It should be stored at room temperature, away from fire or flame, to maintain its integrity and effectiveness. After each use, the cap must be closed tightly to prevent contamination or degradation. It is also important to retain the carton, as it contains essential information regarding the product.

Additional Clinical Information

The product is administered topically, with a recommended application of a thin layer to the affected area every 6 to 8 hours for adults and children over 12 years, not exceeding three applications within a 24-hour period. For children aged 12 years or younger, it is advised to consult a doctor 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, and in the event of ingestion, medical assistance or contact with a Poison Control Center should be sought immediately.

Drug Information (PDF)

This file contains official product information for Aspercreme Lidocaine No-Mess Plus 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 Aspercreme Lidocaine No-Mess Plus 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.