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Extra Strength Gas Relief

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This product has been discontinued

Active ingredient
Dimethicone 125 mg
Other brand names
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2019
Label revision date
January 21, 2021
Active ingredient
Dimethicone 125 mg
Other brand names
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2019
Label revision date
January 21, 2021
Manufacturer
QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)
Registration number
part332
NDC root
63868-854

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Drug Overview

QC Quality Choice is an extra strength gas relief medication that contains simethicone (125 mg), which helps alleviate discomfort, pressure, bloating, and fullness commonly associated with gas. This product is designed to provide you with quick relief from these uncomfortable symptoms, making it easier for you to feel more comfortable throughout your day.

Available in a cherry crème flavor, these chewable tablets are a convenient option for those seeking to manage gas-related discomfort. QC Quality Choice is comparable to Gas-X® Extra Strength, offering a reliable solution for your gas relief needs.

Uses

If you're experiencing discomfort from pressure, bloating, or a feeling of fullness often associated with gas, this medication can help provide relief. It's designed specifically to address these common digestive issues, making your day-to-day life more comfortable.

Rest assured, there are no known teratogenic effects (which means it doesn't cause birth defects) or other nonteratogenic effects associated with this medication. This makes it a safe option for those looking to alleviate gas-related discomfort.

Dosage and Administration

When you need relief, you can chew 1 to 2 tablets of the medication after meals and at bedtime. It's important to chew the tablets completely rather than swallowing them whole, as this helps your body absorb the medication effectively.

Make sure not to take more than 4 tablets in a 24-hour period unless your doctor has advised you to do so. Always follow this guideline to ensure your safety and the best results from the medication.

What to Avoid

There are no specific contraindications, controlled substance classifications, or risks of abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular situations or conditions under which you should avoid using it. Always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

You may experience some side effects while taking this medication. It's important to be aware of potential allergic reactions, which can range from mild skin rashes to more severe responses. If you notice any unusual symptoms, such as difficulty breathing or swelling, seek medical attention immediately.

In addition to allergic reactions, some people may experience cardiovascular issues, such as changes in heart rate or blood pressure. Neurological effects, including headaches or dizziness, can also occur. Other adverse reactions may arise, so it's essential to discuss any concerns with your healthcare provider to ensure your safety while using this medication.

Warnings and Precautions

It’s important to keep this medication out of reach of children to prevent accidental ingestion. Always ensure that it is stored safely and securely.

While there are no specific general precautions or laboratory tests mentioned, it’s essential to stay informed about any potential side effects or interactions with other medications. If you have any concerns or experience unusual symptoms, don’t hesitate to reach out to your healthcare provider for guidance.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the signs of overdose for this medication, general 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 always better to be safe and get checked by a healthcare professional if you have any concerns about your health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be aware that there is no specific information available about the use of this medication during pregnancy. This means that safety concerns, dosage adjustments, or any special precautions have not been established.

Before taking this medication, you should consult with your healthcare provider to discuss any potential risks and to ensure that you are making informed decisions for your health and the health of your baby.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant.

As always, it's a good idea to consult with your healthcare provider if you have any concerns or questions about using any medication while breastfeeding. Your health and the health of your baby are important, and your provider can help you make informed decisions.

Pediatric Use

It's important to keep this medication out of reach of children to ensure their safety. For adults, the recommended dosage is to chew 1 to 2 tablets completely after meals and at bedtime, but you should never swallow the tablets whole.

If you are considering this medication for a child, please consult a physician for guidance, especially regarding the appropriate dosage and any specific recommendations. Remember, do not exceed 4 tablets in a 24-hour period unless directed by a healthcare professional.

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 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.

Always consult your healthcare provider for personalized advice and to ensure that any medications you take are safe and appropriate for your kidney health. They can help you understand how your condition may affect 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 may affect you if you have hepatic impairment (liver issues).

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 you are taking. In this case, there are no specific drug interactions or laboratory test interactions noted, which means that this medication is generally considered safe to use alongside other treatments and tests. However, every individual is different, and your healthcare provider can help ensure that your overall treatment plan is safe and effective for you. Always feel free to ask questions or express any concerns you may have regarding your medications or tests.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to keep it away from excessive heat and moisture, as these conditions can affect its quality and safety.

When handling the product, always do so with clean hands and in a clean environment to maintain its integrity. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

You should take this medication orally by chewing 1 to 2 tablets completely as needed after meals and at bedtime. It's important not to swallow the tablets whole and to avoid exceeding 4 tablets in a 24-hour period unless directed by your doctor. Always follow your physician's advice for safe use.

FAQ

What is QC QUALITY CHOICE used for?

QC QUALITY CHOICE is used for the relief of discomfort, pressure, bloating, and fullness commonly referred to as gas.

What is the active ingredient in QC QUALITY CHOICE?

The active ingredient in QC QUALITY CHOICE is Simethicone, with a dosage of 125 mg.

How should adults take QC QUALITY CHOICE?

Adults should chew 1 to 2 tablets completely as needed after meals and at bedtime, and should not exceed 4 tablets in a 24-hour period unless advised by a physician.

Are there any contraindications for using QC QUALITY CHOICE?

No contraindications are listed for QC QUALITY CHOICE.

Is QC QUALITY CHOICE safe to use during pregnancy or while nursing?

There are no specific warnings or recommendations regarding the use of QC QUALITY CHOICE during pregnancy or for nursing mothers.

What flavor does QC QUALITY CHOICE come in?

QC QUALITY CHOICE is available in Cherry Creme Flavored Chews.

Who distributes QC QUALITY CHOICE?

QC QUALITY CHOICE is distributed by C.D.M.A., Inc., located in Novi, MI.

What should I do if I have questions about QC QUALITY CHOICE?

You can contact customer service at 248-449-9300 for any questions regarding QC QUALITY CHOICE.

How should QC QUALITY CHOICE be stored?

Store QC QUALITY CHOICE at room temperature and protect it from excessive heat and moisture.

Is there a satisfaction guarantee for QC QUALITY CHOICE?

Yes, there is a 100% satisfaction guarantee for QC QUALITY CHOICE.

Packaging Info

Below are the non-prescription pack sizes of Extra Strength Gas Relief (simethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Extra Strength Gas Relief.
Details

Drug Information (PDF)

This file contains official product information for Extra Strength Gas Relief, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Extra Strength Simethicone is formulated to contain 125 mg of simethicone per chew. The dosage form is a chewable tablet, presented in a cherry crème flavor. The product is designed with both natural and artificial flavoring agents to enhance palatability.

Uses and Indications

This drug is indicated for the relief of pressure, bloating, and fullness commonly referred to as gas.

There are no teratogenic or nonteratogenic effects associated with this drug.

Dosage and Administration

Adults are instructed to chew 1 to 2 tablets completely as needed after meals and at bedtime. It is essential that the tablets are not swallowed whole. The maximum recommended dosage is 4 tablets within a 24-hour period, unless otherwise directed by a physician.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

It is imperative to keep this medication out of reach of children to prevent accidental ingestion or misuse. Healthcare professionals should emphasize the importance of safeguarding medications to ensure the safety of pediatric patients.

No specific general precautions or laboratory tests have been identified for this medication. Therefore, healthcare providers are encouraged to remain vigilant and monitor patients for any adverse effects or unusual symptoms that may arise during treatment.

In the absence of detailed emergency medical help instructions or directives to discontinue use and consult a physician, practitioners should exercise clinical judgment and advise patients to seek medical attention if they experience any concerning reactions or side effects.

Side Effects

Patients may experience a range of adverse reactions associated with the use of this medication. Serious adverse reactions include allergic reactions, which can manifest in various forms and may require immediate medical attention.

Cardiovascular events have also been reported, necessitating careful monitoring of patients with pre-existing cardiovascular conditions. Neurological adverse reactions may occur, and patients should be advised to report any unusual neurological symptoms promptly.

In addition to these serious reactions, other adverse reactions have been noted in clinical trials and postmarketing experiences. It is essential for healthcare providers to remain vigilant and consider these potential reactions when prescribing this medication.

Drug Interactions

No specific drug interactions have been identified for this medication. Additionally, there are no reported interactions with laboratory tests. Therefore, no dosage adjustments or monitoring recommendations are necessary based on drug or laboratory test interactions.

Packaging & NDC

Below are the non-prescription pack sizes of Extra Strength Gas Relief (simethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Extra Strength Gas Relief.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. The dosing instructions are primarily designed for adults, who are directed to chew 1 to 2 tablets completely as needed after meals and at bedtime, without swallowing the tablets whole. It is important to note that the maximum dosage should not exceed 4 tablets in a 24-hour period unless specifically advised and supervised by a physician. There is no established dosing or safety information for pediatric patients, and caution should be exercised when considering this medication for use in children.

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

There is no specific information regarding the use of this medication during pregnancy, including safety concerns, dosage modifications, or special precautions. Healthcare professionals should consider the lack of data when prescribing this medication to pregnant patients. The potential risks and benefits should be carefully evaluated, and alternative treatments may be considered in the absence of established safety profiles. Women of childbearing potential should be counseled on the importance of effective contraception during treatment.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

Patients with renal impairment have no specific information regarding dosage adjustments, special monitoring, or safety considerations provided in the text. Therefore, healthcare professionals should exercise caution and consider individual patient factors when prescribing to this population. Regular assessment of renal function may be warranted to ensure safe and effective use of the medication in patients with reduced kidney function.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in clinical trials for this medication. Consequently, there is no available information regarding dosage adjustments, special monitoring requirements, or precautions 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 warranted based on clinical judgment.

Overdosage

In the absence of specific information regarding overdosage, healthcare professionals are advised to exercise caution when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks associated with overdosage.

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 compound in these areas.

Postmarketing Experience

No postmarketing experience details are available in the provided data.

Patient Counseling

Advise patients that no specific counseling information is available at this time. Encourage them to reach out with any questions or concerns regarding their treatment or medication. It is important for patients to maintain open communication with their healthcare provider to ensure they receive the most appropriate care tailored to their individual needs.

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, ensuring that it is protected from excessive heat and moisture to maintain its integrity and efficacy. Proper handling and storage conditions are crucial for preserving the quality of the product throughout its shelf life.

Additional Clinical Information

The medication is administered orally, with adults instructed to chew 1 to 2 tablets completely as needed after meals and at bedtime. It is important that patients do not swallow the tablets whole and do not exceed a maximum of 4 tablets within a 24-hour period unless advised and supervised by a physician.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Extra Strength Gas Relief, 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 Extra Strength Gas Relief, 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.