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Quality Choice

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Active ingredient
Lidocaine Hydrochloride 4 g/100 g
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 2025
Label revision date
July 11, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Lidocaine Hydrochloride 4 g/100 g
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 2025
Label revision date
July 11, 2025
Manufacturer
CHAIN DRUG MARKETING ASSOCIATION
Registration number
M017
NDC root
83324-226
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

QUALITY CHOICE® is a topical pain relief product that contains 4% lidocaine HCl (a local anesthetic that helps numb the skin). It is designed for the temporary relief of minor pain in affected areas, making it a convenient option for those seeking quick pain relief. The roll-on applicator allows for easy application without the need for direct contact, and the formula is free from oils, parabens, and alcohol, ensuring a clean and odor-free experience.

This product is comparable to Aspercreme® Odor Free, providing maximum strength pain relief with the added benefit of aloe to soothe the skin. Whether you're dealing with muscle aches, joint pain, or other minor discomforts, QUALITY CHOICE® aims to help you feel more comfortable and at ease.

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) or nonteratogenic effects associated with this medication.

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 three 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

It's important to use this product safely to avoid potential issues. You should not use it on large areas of your body, on cut, irritated, or swollen skin, or on puncture wounds. Additionally, if you need to use it for more than one week, please consult your doctor first.

While using this product, make sure to keep it away from your eyes and avoid bandaging or applying heat, like heating pads, to the treated area. Remember, this product is flammable, so keep it away from fire or flames to ensure your safety.

Side Effects

When using this product, it's important to be aware of some potential side effects and safety precautions. You should only apply it to the skin and avoid using it on large areas, cut or irritated skin, or puncture wounds. If your condition worsens, persists for more than seven days, or returns shortly after improvement, stop using the product and consult a doctor.

Additionally, take care to avoid contact with your eyes, and do not apply heat or bandage the area where the product is used. Remember that this product is flammable, so keep it away from fire or flames. If swallowed, seek medical help immediately or contact a Poison Control Center at 1-800-222-1222.

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.

If your condition worsens, or if your symptoms last longer than 7 days or return after clearing up, stop using the product and reach out to your doctor. Additionally, if the product is swallowed, seek emergency medical help immediately or contact a Poison Control Center at 1-800-222-1222. Remember, 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 immediately. You can contact a Poison Control Center at 1-800-222-1222 for guidance.

Signs of an overdose may include unusual symptoms, but specific details about 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 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 children over 12 and adults, you can apply a thin layer to the affected area every 6 to 8 hours, but be careful not to exceed three applications in a 24-hour period. 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 you understand how to manage your treatment effectively while considering your kidney 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 differently due to your liver health.

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

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that the medication is generally considered safe to use with other drugs and tests. However, every individual is different, and your healthcare provider can help ensure that your treatment plan is safe and effective for you.

Always discuss any new medications or tests with your healthcare provider to avoid any potential issues and to ensure that you receive the best care possible.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. This means keeping it in a place that is neither too hot nor too cold, typically between 68°F and 77°F (20°C to 25°C).

When handling the product, make sure to do so with clean hands and in a clean environment to maintain its safety and effectiveness. Always follow any specific instructions provided with the product for proper use and disposal.

Additional Information

No further information is available.

FAQ

What is QUALITY CHOICE® used for?

QUALITY CHOICE® is used for the temporary relief of minor pain.

How should I apply QUALITY CHOICE®?

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 QUALITY CHOICE®?

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

Are there any warnings for using QUALITY CHOICE®?

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

What should I do if I experience side effects?

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

Is QUALITY CHOICE® flammable?

Yes, keep QUALITY CHOICE® away from fire or flame.

What should I do if QUALITY CHOICE® is swallowed?

Get medical help or contact a Poison Control Center immediately at 1-800-222-1222.

Can I use QUALITY CHOICE® if I am pregnant or breastfeeding?

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

What are the ingredients in QUALITY CHOICE®?

QUALITY CHOICE® contains 4% lidocaine HCl, which is a local anesthetic that temporarily relieves minor pain.

Where can I find more information about QUALITY CHOICE®?

You can visit the website www.qualitychoice.com for more information.

Packaging Info

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

Packaging configurations for Quality Choice.
Details

Drug Information (PDF)

This file contains official product information for Quality Choice, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

NDC# 83324-226-71. QUALITY CHOICE® is a maximum strength pain relief formulation containing 4% lidocaine hydrochloride. This roll-on dosage form is designed for the temporary relief of pain in affected areas. The product features a no-touch applicator and is formulated to be oil-free, paraben-free, alcohol-free, and odor-free, with the addition of aloe. Each container has a net weight of 2.5 oz (71 g). Distributed by CDMA, Inc., Novi, MI 48375. For more information, visit www.qualitychoice.com. This product is not manufactured or distributed by Chattem, Inc., owner of the registered trademark Aspercreme® Odor Free with 4% Lidocaine.

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 and younger, it is recommended to consult a physician before use.

Contraindications

Use of this product 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 adverse reactions. The product should not be applied to puncture wounds, as this may lead to complications. Prolonged use beyond one week without consulting a healthcare professional is also contraindicated to prevent potential risks associated with extended exposure.

During use, contact with the eyes must be avoided to prevent irritation or injury. Additionally, the area of application should not be bandaged or subjected to local heat, such as heating pads, as this may exacerbate adverse effects.

Due to its flammable nature, the product must be kept away from fire or flame to ensure safety.

Warnings and Precautions

For external use only. This product is contraindicated for application on large areas of the body, as well as on cut, irritated, or swollen skin. It should not be used on puncture 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 advice if the condition worsens, if symptoms persist for more than seven days, or if symptoms resolve and then recur within a few days.

In the event of accidental ingestion, immediate medical assistance should be sought, or the Poison Control Center should be contacted at 1-800-222-1222.

This product is flammable; therefore, it is essential to keep it away from fire or flame to prevent any hazardous situations.

Side Effects

Patients using this product should be aware that it is intended for external use only. It is contraindicated for application on large areas of the body, on cut, irritated, or swollen skin, and on puncture wounds. Prolonged use beyond one week without consulting a healthcare professional is not recommended.

During the use of this product, patients should avoid contact with the eyes and refrain from bandaging or applying local heat, such as heating pads, to the area of application.

Patients are advised to discontinue use and seek medical advice if their condition worsens, if symptoms persist for more than seven days, or if symptoms resolve and then recur within a few days.

Additionally, the product is flammable; therefore, it should be kept away from fire or flame. In the event of accidental ingestion, patients should seek immediate medical assistance or contact a Poison Control Center at 1-800-222-1222.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on the current information.

Packaging & NDC

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

Packaging configurations for Quality Choice.
Details

Pediatric Use

Pediatric patients 12 years and younger should consult a healthcare professional prior to use. For adolescents and adults 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.

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 those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully weighed, as the effects on fetal outcomes and lactation are not fully established. It is essential for women of childbearing potential to seek medical advice to ensure the safety of both the mother and the developing fetus.

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 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 are advised to seek medical help or contact a Poison Control Center without delay. The national Poison Control Center can be reached at 1-800-222-1222 for 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 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 specific non-teratogenic effects have been identified. Additionally, there are no detailed findings related to nonclinical toxicology or animal pharmacology and toxicology available.

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 and pets to prevent accidental ingestion or misuse. 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 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. They should be advised to stop use and seek medical advice if their condition worsens or 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 instructed to follow all directions and warnings provided on the carton carefully. They should be cautioned to avoid contact with the eyes and not to bandage or apply local heat, such as heating pads, to the area of use. Additionally, patients should be reminded to keep the product away from fire or flame to ensure safety during use.

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

No further data are available.

Drug Information (PDF)

This file contains official product information for Quality Choice, 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 Quality Choice, 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

Last AI update:

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.