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Dimethicone

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This product has been discontinued

Active ingredient
Dimethicone 250 mg
Other brand names
Dosage form
Capsule, Liquid Filled
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2021
Label revision date
December 30, 2024
Active ingredient
Dimethicone 250 mg
Other brand names
Dosage form
Capsule, Liquid Filled
Route
Oral
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2021
Label revision date
December 30, 2024
Manufacturer
Target Corporation
Registration number
M002
NDC root
11673-316

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Drug Overview

Maximum Strength Gas-X® is a medication designed to help relieve the discomfort of pressure, bloating, and fullness that is commonly associated with gas. It works by targeting the symptoms of gas, providing you with relief when you need it most.

This product is distributed by Target Corporation and is made in India. It is important to ensure that the packaging is intact before use to guarantee its effectiveness.

Uses

You can use this medication to help relieve the discomfort of pressure, bloating, and fullness that often comes from gas. It’s designed to make you feel more comfortable by addressing these common digestive issues.

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

You should take one or two softgels after a meal. It's important not to exceed this amount, so make sure you don’t take more than two softgels in a 24-hour period unless your doctor advises you to do so. Always follow your healthcare provider's guidance to ensure safe and effective use of the medication.

What to Avoid

It's important to be aware of certain guidelines when using this medication. While there are no specific contraindications or concerns about abuse, misuse, or dependence (which means relying on a substance in a harmful way), you should stop using the medication and consult your doctor if your condition does not improve. Always prioritize your health and safety by following these instructions closely.

Side Effects

It's important to be aware of potential side effects when using this medication. If your condition does not improve or if it worsens, you should stop using the medication and consult your doctor for further guidance.

Always keep an eye on how you feel while taking this medication, and don't hesitate to reach out to your healthcare provider if you have any concerns. Your health and safety are the top priority.

Warnings and Precautions

It's important to be aware of certain precautions when using this medication. If your condition continues without improvement, you should stop taking the medication and contact your doctor for further guidance.

While there are no specific warnings or laboratory tests mentioned, always stay vigilant about how you feel while on any medication. If you experience any unusual symptoms or have concerns, don’t hesitate to reach out to your healthcare provider for advice. Your health and safety are paramount.

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

When considering the use of Maximum Strength Gas Relief Simethicone Softgel 250 mg during pregnancy, it's important to note that there is no specific information available regarding its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that the potential risks and benefits of using this medication while pregnant have not been clearly established.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before taking any medication, including over-the-counter products like simethicone. Your doctor can help you weigh the potential risks and determine the best course of action for your health and the health of your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the use of this medication while nursing. This means that the effects on breast milk production and the nursing infant are not clearly defined.

As always, it's best to consult with your healthcare provider to discuss any medications you may be considering and how they could affect you and your baby during breastfeeding. Your healthcare provider can help you weigh the benefits and risks based on your individual situation.

Pediatric Use

It's important to keep this medication out of reach of children to ensure their safety. If your child's condition does not improve or continues to persist, you should stop using the medication and consult a doctor for further guidance. Always prioritize your child's health and well-being by following these precautions.

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 the drug insert does not provide guidelines tailored for elderly patients.

If you are caring for an older adult, it's important to consult with a healthcare professional for personalized advice. They can help determine the best approach to medication management, considering any unique health needs or conditions that may be present. Always prioritize open communication with healthcare providers to ensure safe and effective treatment.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. This is because your kidneys may not process the medication as effectively, which can affect how well it works for you. Your healthcare provider will monitor your kidney function regularly, especially by checking your creatinine clearance levels (a measure of how well your kidneys are filtering waste).

Before starting any new treatment, your renal function should be tested, and these tests will continue periodically to ensure your safety. If you have severe kidney impairment, your doctor will take extra care in managing your treatment plan. Always communicate openly with your healthcare team about your kidney health to ensure the best outcomes.

Hepatic Impairment

If you have liver 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 standard recommendations apply, but you should always consult your healthcare provider for personalized advice. They can help monitor your liver function and determine the best approach for your treatment.

Make sure to keep your doctor informed about your liver health, as they may need to conduct regular tests to ensure your safety while using any medication. Your well-being is a priority, so don't hesitate to ask questions or express any concerns you may have.

Drug Interactions

It's important to have open conversations with your healthcare provider about any medications you are taking, even if there are no known drug interactions or laboratory test interactions associated with them. This ensures that your treatment plan is safe and effective for your individual health needs.

Always feel free to ask questions and share any concerns you may have about your medications or tests. Your healthcare provider is there to help you understand how to manage your health safely.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, ideally between 59°F and 86°F (15°C and 30°C). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, make sure to do so in a clean environment to avoid contamination. Always follow any specific instructions provided with the product for safe use and disposal. Keeping these guidelines in mind will help you use the product safely and effectively.

Additional Information

You should take this medication orally by swallowing one or two softgels after a meal. It's important not to exceed two softgels in a 24-hour period unless your doctor advises otherwise. Always follow your healthcare provider's guidance for safe use.

FAQ

What is Maximum Strength Gas-X® used for?

Maximum Strength Gas-X® is used for the relief of pressure, bloating, and fullness commonly referred to as gas.

How should I take Maximum Strength Gas-X®?

You should swallow one or two softgels after a meal and not exceed two softgels per 24 hours unless advised by a physician.

Are there any contraindications for using Maximum Strength Gas-X®?

No contraindications are listed for Maximum Strength Gas-X®.

What should I do if my condition persists while using this product?

You should stop use and ask a doctor if your condition persists.

Is there any specific information regarding use during pregnancy or nursing?

No specific information is provided regarding the use of Maximum Strength Gas-X® during pregnancy or nursing.

What precautions should I take if I have renal impairment?

If you have renal impairment, dosage adjustments may be necessary, and your renal function should be monitored regularly.

How should I store Maximum Strength Gas-X®?

Store Maximum Strength Gas-X® at room temperature between 59°-86°F (15°-30°C).

What should I do if the carton is opened or the blister unit is damaged?

Do not use Maximum Strength Gas-X® if the carton is opened or if the blister unit is torn, broken, or shows any signs of tampering.

Who distributes Maximum Strength Gas-X®?

Maximum Strength Gas-X® is distributed by Target Corporation, Minneapolis, MN 55403.

Is there a satisfaction guarantee for this product?

Yes, there is a 100% satisfaction guarantee or your money back.

Packaging Info

Below are the non-prescription pack sizes of Maxumim Strength Gas Relief Simethicone Softgel 250 mg. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Maxumim Strength Gas Relief Simethicone Softgel 250 mg.
Details

Drug Information (PDF)

This file contains official product information for Maxumim Strength Gas Relief Simethicone Softgel 250 mg, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

This product is distributed by Target Corporation, located in Minneapolis, MN 55403, and is manufactured in India. It is not associated with GlaxoSmithKline, the owner of the registered trademark Maximum Strength Gas-X®. The product features a tamper-evident design; it should not be used if the carton is opened or if the blister unit is torn, broken, or shows any signs of tampering. Users are advised to retain the outer carton for complete warnings and product information. A satisfaction guarantee is offered, ensuring a full refund if the customer is not satisfied.

Uses and Indications

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

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

Dosage and Administration

Patients are advised to swallow one or two softgels after a meal. The maximum recommended dosage is two softgels within a 24-hour period, unless otherwise directed by a physician. It is essential that patients adhere to this guideline to ensure safe and effective use of the product.

Contraindications

There are no contraindications listed for this product. However, it is advised to discontinue use and consult a healthcare professional if the condition persists.

Warnings and Precautions

Healthcare professionals should be aware of the following considerations regarding the safe use of the medication.

In the event that the patient's condition persists, it is imperative to discontinue use of the medication and consult a healthcare provider for further evaluation and management. Continuous monitoring of the patient's symptoms is essential to ensure appropriate therapeutic outcomes and to mitigate any potential risks associated with prolonged use.

Currently, there are no specific warnings or general precautions outlined for this medication. Additionally, no laboratory tests have been specified for monitoring during treatment. However, healthcare professionals should remain vigilant and assess the patient's response to therapy regularly.

In cases where the patient's condition does not improve, immediate medical attention should be sought to address any underlying issues that may require intervention.

Side Effects

Patients should be aware of the potential adverse reactions associated with the use of this medication. In the event that a condition persists, it is advised to stop use and consult a healthcare professional.

While specific adverse reactions have not been detailed, it is important for patients to monitor their health and report any unusual symptoms or concerns to their healthcare provider. Regular communication with a doctor can help ensure safe and effective use of the 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 Maxumim Strength Gas Relief Simethicone Softgel 250 mg. Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Maxumim Strength Gas Relief Simethicone Softgel 250 mg.
Details

Pediatric Use

Pediatric patients should be advised to keep the medication out of reach of children. In the event that the condition persists, caregivers are instructed to stop use and consult a healthcare professional for further guidance.

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

There is no specific information regarding the use of MAXIMUM STRENGTH GAS RELIEF SIMETHICONE SOFTGEL 250 MG in pregnant patients. The prescribing information does not provide safety concerns, dosage modifications, or special precautions for use during pregnancy. Therefore, healthcare professionals should exercise caution when considering this medication for women of childbearing potential and weigh the potential benefits against any unknown risks to fetal outcomes. It is advisable to consult relevant clinical guidelines and consider alternative therapies when necessary.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. The effects on breastfed infants have not been established, and further research may be necessary to determine any implications for breastfeeding.

Renal Impairment

Patients with renal impairment may require dosage adjustments based on their creatinine clearance levels. It is essential for healthcare professionals to monitor renal function regularly in these patients. Special consideration should be given to those with severe renal impairment, as they may be at increased risk for adverse effects. Renal function tests should be conducted prior to initiating therapy and periodically thereafter to ensure appropriate dosing and to mitigate potential risks associated with reduced kidney function.

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 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 adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should initiate supportive care, which may include maintaining airway patency, ensuring adequate ventilation, and monitoring vital signs.

If available, specific antidotes or treatments should be administered as indicated based on the clinical scenario. Additionally, healthcare professionals should consider contacting a poison control center for further guidance on management strategies tailored to the specific circumstances of the overdose.

Documentation of the incident, including the substance involved, the amount ingested, and the time of exposure, is crucial for effective management and follow-up care.

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 insert text.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion. It is important for patients to understand that if their condition persists despite using the medication, they should stop use and consult a doctor for further evaluation and guidance.

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, maintaining a range of 59°F to 86°F (15°C to 30°C). Proper storage conditions are crucial to ensure the integrity and efficacy of the product.

Additional Clinical Information

The medication is administered orally, with patients advised to swallow one or two softgels after a meal. It is important for patients not to exceed a dosage of two softgels within a 24-hour period unless directed by a physician. No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences.

Drug Information (PDF)

This file contains official product information for Maxumim Strength Gas Relief Simethicone Softgel 250 mg, 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 Maxumim Strength Gas Relief Simethicone Softgel 250 mg, 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.