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Up and up Extra Strength Gas Relief Cherry 134

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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 2024
Label revision date
June 13, 2024
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 2024
Label revision date
June 13, 2024
Manufacturer
Target corporation
Registration number
part332
NDC root
82442-134

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Drug Overview

up&up Extra Strength Gas Relief contains simethicone, a medication designed to provide fast relief from gas pressure, bloating, and discomfort. Each chewable tablet contains 125 mg of simethicone, which works by breaking up gas bubbles in your stomach and intestines, making it easier for your body to eliminate them.

This product is comparable to the active ingredient found in Gas-X and is available in a pleasant cherry flavor. It comes in a package of 48 chewable tablets, making it a convenient option for managing symptoms associated with gas.

Uses

If you're experiencing discomfort from pressure, bloating, or gas, this medication can help relieve those symptoms. It works effectively to ease the feeling of fullness and the discomfort associated with gas buildup in your digestive system. You can feel more comfortable and at ease after using it, allowing you to go about your day without the distraction of these issues.

Dosage and Administration

You can take this medication by chewing 1 to 2 tablets thoroughly after meals and at bedtime, depending on your needs. It's important to remember not to exceed 4 tablets in a 24-hour period unless your doctor has advised you otherwise. 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 precautions when using this medication. While there are no specific contraindications or risks of abuse, misuse, or dependence associated with it, you should take care to avoid any potential overdose. If you suspect an overdose, seek medical help or contact a poison control center immediately. Your safety is paramount, so always use the medication as directed.

Side Effects

You may experience some side effects while taking this medication. Common reactions include allergic responses, which can range from mild skin rashes to more severe symptoms. Serious side effects may involve cardiovascular issues, such as changes in heart rate or blood pressure, and neurological effects, which can include headaches or dizziness.

It's important to be aware that some individuals may have more severe allergic reactions, known as anaphylaxis (a life-threatening reaction that requires immediate medical attention). If you notice any unusual symptoms or have concerns about your health while using this medication, please consult your healthcare provider for guidance.

Warnings and Precautions

It's important to be aware of certain precautions when using this medication. If you suspect an overdose, seek emergency medical help or contact a poison control center right away. This is crucial for your safety.

While there are no specific warnings or general precautions listed, always stay vigilant about how you feel while taking any medication. If you experience any unusual symptoms or have concerns, 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 effects of an overdose for this medication, you should be aware of general signs that may indicate a problem. These can include unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms or if you believe you have taken too much of the medication, seek medical help right away. Contact your healthcare provider or go to the nearest emergency room. It's always better to be safe and get checked out if you have any concerns about your health.

Pregnancy Use

If you are pregnant or planning to become pregnant, it's important to be cautious with any medications, including over-the-counter products like Up and Up Extra Strength Gas Relief Cherry, which contains simethicone. The drug insert does not provide specific information about its safety during pregnancy, including any potential risks or necessary dosage adjustments.

Since there are no detailed guidelines or precautions mentioned, it’s best to consult your healthcare provider before using this product. They can help you weigh the benefits and risks based on your individual health needs.

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 effects of this medication on nursing mothers or lactation (the process of producing breast milk). Since there are no guidelines or data provided, it’s advisable to consult with your healthcare provider to discuss any potential risks or concerns related to your situation. They can help you make informed decisions about your health and your baby's well-being.

Pediatric Use

It's important to keep this medication out of reach of children to prevent accidental ingestion. If you suspect an overdose, seek medical help or contact a poison control center right away. For children who are able to chew tablets, they can take 1 to 2 tablets thoroughly after meals and at bedtime, but be sure not to exceed 4 tablets in a 24-hour period unless directed by a doctor. Always consult with a healthcare professional if you have any questions or concerns about your child's use of this medication.

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 to using this medication safely and effectively, taking into account any unique health needs or conditions that may be present. Always prioritize open communication with your healthcare team to ensure the best outcomes.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. Specifically, if you have reduced creatinine clearance (a measure of how well your kidneys are filtering waste), your healthcare provider will closely monitor your condition. Regular renal function tests (tests that check how well your kidneys are working) should be performed to ensure your safety.

For those with significant renal impairment, a reduced dose of medication is recommended. Always communicate with your healthcare team about your kidney health to ensure you receive the appropriate care and 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 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 function and how it relates to your treatment. They can help ensure that your medication is safe and effective for you.

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 changes in your medications or health status with your healthcare provider to avoid any potential issues and to get the best care possible.

Storage and Handling

To ensure the safety and effectiveness of your product, it's important to store it properly. Keep it at room temperature, away from high humidity and excessive heat—specifically, temperatures above 40ºC (104ºF). This will help maintain its quality and performance.

When handling the product, be cautious not to use it if any individual blister unit is broken or open, as this could compromise its safety. Following these guidelines will help you use the product effectively and safely.

Additional Information

You can take this medication orally by chewing 1 to 2 tablets thoroughly as needed after meals and at bedtime. However, be sure not to exceed 4 tablets in a 24-hour period unless directed by your doctor. Always follow your healthcare provider's advice regarding the use of this medication.

FAQ

What is up&up Extra Strength Gas Relief?

It is a medication containing simethicone, 125 mg chewable tablets, designed to provide fast relief from gas pressure, bloating, and discomfort.

How should I take up&up Extra Strength Gas Relief?

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

What symptoms does this medication relieve?

It relieves pressure, bloating, and symptoms referred to as gas.

Are there any contraindications for using this medication?

No contraindications are listed for up&up Extra Strength Gas Relief.

What should I do in case of an overdose?

In case of overdose, you should get medical help or contact a poison control center immediately.

Is there any information regarding use during pregnancy or nursing?

No specific information is provided regarding the use of this medication during pregnancy or nursing.

How should I store up&up Extra Strength Gas Relief?

Store it at room temperature, avoiding high humidity and excessive heat above 40ºC (104ºF).

What flavor does this medication come in?

It comes in a cherry flavor.

What is the package information for this medication?

It is available in a package of 48 chewable tablets.

Are there any specific warnings or precautions I should be aware of?

No specific warnings or precautions are provided in the text.

Packaging Info

Below are the non-prescription pack sizes of Up and up Extra Strength Gas Relief Cherry 134 (simethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Up and up Extra Strength Gas Relief Cherry 134.
Details

Drug Information (PDF)

This file contains official product information for Up and up Extra Strength Gas Relief Cherry 134, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

Simethicone is presented in the form of chewable tablets, each containing 125 mg of the active ingredient. The tablets are formulated with a cherry flavor to enhance palatability. Each bottle contains a total of 48 chewable tablets, providing a convenient dosage form for administration.

Uses and Indications

This drug is indicated for the relief of pressure, bloating, and symptoms associated with gas.

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

Dosage and Administration

Patients should chew 1 to 2 tablets thoroughly as needed after meals and at bedtime. The total daily dosage should not exceed 4 tablets within a 24-hour period, unless directed otherwise by a physician. It is essential for healthcare professionals to monitor patients for adherence to this dosing regimen to ensure safety and efficacy.

Contraindications

There are no specific contraindications listed for this product. However, in the event of an overdose, it is imperative to seek medical assistance or contact a poison control center immediately.

Warnings and Precautions

In the event of an overdose, it is imperative to seek emergency medical assistance or contact a poison control center immediately. Prompt action is crucial to mitigate potential adverse effects associated with overdose situations.

Healthcare professionals are advised to remain vigilant and monitor patients for any signs of overdose, ensuring that appropriate interventions are initiated without delay.

Side Effects

Patients may experience a range of adverse reactions associated with the use of this medication. Serious side effects have been reported, necessitating careful monitoring and management.

Common adverse reactions observed in clinical trials include various cardiovascular, neurological, and dermatologic effects. These reactions may manifest in different ways, and patients should be informed of the potential for allergic reactions, which can occur in some individuals.

In addition to the reactions noted in clinical trials, postmarketing experience has revealed additional adverse reactions that may not have been fully characterized during the initial studies. It is important for healthcare providers to remain vigilant for these reactions in patients receiving the medication.

Overall, the safety profile of the medication includes a spectrum of adverse reactions, and both healthcare providers and patients should be aware of the potential for serious and common side effects, as well as the possibility of allergic reactions and other important notes regarding its use.

Drug Interactions

No specific drug interactions have been identified in the available data. Additionally, there are no reported interactions between the drug and 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 Up and up Extra Strength Gas Relief Cherry 134 (simethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Up and up Extra Strength Gas Relief Cherry 134.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. In the event of an overdose, immediate medical assistance or contact with a poison control center is essential.

For dosing, pediatric patients may chew 1 to 2 tablets thoroughly as needed after meals and at bedtime. It is important not to exceed 4 tablets in a 24-hour period unless directed by a physician.

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 Up and Up Extra Strength Gas Relief Cherry 134 (simethicone) during pregnancy. The drug insert does not provide safety concerns, dosage modifications, or special precautions for pregnant patients. Therefore, healthcare professionals should exercise caution when considering the use of this product in pregnant individuals, as the potential effects on fetal outcomes are not established. Women of childbearing potential should be advised to consult their healthcare provider before using this medication.

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

Renal impairment may necessitate dosage adjustments for patients with reduced kidney function. It is essential that patients with reduced creatinine clearance are closely monitored to ensure safety and efficacy. Regular renal function tests should be performed in patients with kidney problems to assess their condition. A reduced dose is recommended for patients with significant renal impairment to mitigate the risk of adverse effects.

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 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 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 monitoring vital signs, providing symptomatic treatment, and ensuring the patient's safety.

If available, consultation with a poison control center or a medical toxicologist is recommended to guide further management and treatment options.

Documentation of the incident, including the substance involved, the amount taken, and the time of ingestion, 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 seek immediate medical assistance or contact a poison control center in the event of an overdose. It is crucial for patients to understand the importance of prompt action in such situations to ensure their safety and well-being.

Storage and Handling

The product is supplied in individual blister units. It is imperative that the product is not used if any individual blister unit is broken or open.

For optimal storage, the product should be kept at room temperature. It is essential to avoid exposure to high humidity and excessive heat, specifically temperatures exceeding 40ºC (104ºF), to maintain the integrity of the product.

Additional Clinical Information

The medication is administered orally, with patients advised to chew 1 to 2 tablets thoroughly as needed after meals and at bedtime. It is important not to exceed 4 tablets within a 24-hour period unless directed by a physician. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Up and up Extra Strength Gas Relief Cherry 134, 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 Up and up Extra Strength Gas Relief Cherry 134, 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.