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Alka-Seltzer Kids Tummy Reliefchews

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Active ingredients
  • Dimethicone 80 mg
  • Calcium Carbonate 750 mg
Other brand names
Drug classes
Blood Coagulation Factor, Phosphate Binder
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2021
Label revision date
December 4, 2025
Drug Information (PDF)
Prescribing information, PDF file
Active ingredients
  • Dimethicone 80 mg
  • Calcium Carbonate 750 mg
Other brand names
Drug classes
Blood Coagulation Factor, Phosphate Binder
Dosage form
Tablet, Chewable
Route
Oral
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 2021
Label revision date
December 4, 2025
Manufacturer
Bayer HealthCare LLC.
Registration number
M001
NDC root
0280-0051
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

Alka-Seltzer® Kids Tummy Relief Chews® are chewable tablets designed to help relieve common stomach issues in children. They contain calcium carbonate, which acts as an antacid to neutralize stomach acid, and simethicone, which helps reduce gas and bloating. These chews are available in a tasty fruit punch flavor and are formulated to provide fast relief from symptoms such as acid indigestion, heartburn, sour stomach, and upset stomach, as well as the discomfort associated with gas.

With claims of working "Amazingly Fast!" and offering relief from six different symptoms, Alka-Seltzer® Kids Tummy Relief Chews® can be a helpful option for parents looking to soothe their child's tummy troubles.

Uses

You can use this medication to help relieve several uncomfortable digestive issues. It is effective for easing acid indigestion, heartburn, and a sour stomach. If you're experiencing an upset stomach related to these symptoms, this medication can provide relief. Additionally, it helps with bloating, pressure, or that stuffed feeling often associated with gas.

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 aged 12 years and older, you can take 1 or 2 chewable tablets when you experience symptoms, or as your doctor advises. However, make sure not to exceed 6 chewable tablets in a 24-hour period.

For children aged 6 to under 12 years, they should take 1 chewable tablet under adult supervision when symptoms arise, or as directed by a doctor. It's important to limit their intake to no more than 4 chewable tablets in a 24-hour period. If your child is under 6 years old, you should consult a doctor before giving them any medication.

If you are pregnant, remember to also limit your intake to a maximum of 6 chewable tablets in a 24-hour period. Always follow these guidelines to ensure safe and effective use of the medication.

What to Avoid

You should avoid using this product if you have ever had an allergic reaction to it or any of its ingredients. For safe use, adults and children aged 12 and over should not take more than 6 chewable tablets in a 24-hour period, while children aged 6 to under 12 should limit their intake to 4 chewable tablets in the same timeframe. If you are pregnant, you should also not exceed 6 chewable tablets in 24 hours. Additionally, do not use the maximum dosage for more than 2 weeks unless directed by a physician.

It's important to keep this product out of reach of children to prevent accidental ingestion. Always follow these guidelines to ensure your safety and well-being.

Side Effects

It's important to be aware of potential side effects when considering this medication. You should not use this product if you have ever experienced an allergic reaction to it or any of its ingredients. Allergic reactions can range from mild symptoms, like rashes, to severe reactions that may require immediate medical attention.

Always consult with your healthcare provider if you have any concerns about allergies or side effects related to this medication. Your safety is a priority, and understanding these warnings can help you make informed decisions about your health.

Warnings and Precautions

You should not use this product if you have ever had an allergic reaction to it or any of its ingredients. It's important to talk to your doctor or pharmacist before using this product, especially if you are currently taking any prescription medications, as antacids can interact with certain drugs. If you are pregnant or breastfeeding, make sure to inform your doctor that you are using this product. Always keep it out of reach of children to ensure their safety.

There are no specific laboratory tests required for this product, but if you experience any unusual symptoms or have concerns, it's best to consult your healthcare provider.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's always important to be aware of the signs of an overdose, which can include unusual drowsiness, confusion, or difficulty breathing. If you suspect that you or someone else may have taken too much of a medication, it’s crucial to seek immediate medical help.

In case of an overdose, contact your local emergency services or go to the nearest hospital. Having the medication packaging or information on hand can help medical professionals provide the best care. Always remember that when it comes to medications, it's better to be safe and get help if you have any concerns.

Pregnancy Use

If you are pregnant or breastfeeding, it’s important to let your doctor know that you are using this product. This information helps ensure your safety and the safety of your baby, as certain medications can affect pregnancy or breastfeeding. Always consult your healthcare provider for guidance tailored to your specific situation.

Lactation Use

If you are pregnant or breastfeeding, it's important to let your doctor know that you are using this product. This information helps ensure your safety and the well-being of your baby. Always consult with your healthcare provider about any medications or products you are using while nursing, as they can provide guidance tailored to your specific situation.

Pediatric Use

When giving this medication to children aged 6 to under 12 years, you should ensure they do not take more than 4 chewable tablets in a 24-hour period. Under adult supervision, they can chew and swallow 1 tablet as needed for symptoms or as directed by a doctor.

For children under 6 years old, it’s important to consult a doctor before administering this medication. Always follow these guidelines to ensure your child's safety and well-being.

Geriatric Use

When considering Alka-Seltzer Kids Tummy Relief Chews for older adults, it's important to note that the drug insert does not provide specific information about its use in this age group. This means that there may not be established guidelines or dosage recommendations tailored for older adults.

If you are caring for an older adult, it's always best to consult with a healthcare professional before starting any new medication. They can help determine the safest and most effective options based on individual health needs and any existing conditions.

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 determine the best course of action based on your kidney function and overall 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 if you have hepatic impairment (issues with liver function).

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 be aware that some over-the-counter medications, such as antacids containing calcium carbonate, can interact with prescription drugs. These interactions may change how well your prescription medications work. Because of this, it's crucial to discuss all the medications you are taking, including any antacids, with your healthcare provider.

By having an open conversation about your medications, you can help ensure that you receive the best possible care and avoid any potential issues with drug effectiveness. Always keep your healthcare provider informed about any changes in your medication routine.

Storage and Handling

To ensure the best performance of your product, store it at room temperature, keeping it away from excessive heat—specifically, temperatures above 40°C (104°F). This helps maintain its effectiveness and safety.

After each use, make sure to close the cap tightly. This simple step helps prevent contamination and preserves the integrity of the product. Always handle it with care to ensure your safety and the product's reliability.

Additional Information

No further information is available.

FAQ

What is Alka-Seltzer® Kids Tummy ReliefChews® used for?

Alka-Seltzer® Kids Tummy ReliefChews® is used for relief of acid indigestion, heartburn, sour stomach, upset stomach, and bloating or gas.

What are the active ingredients in Alka-Seltzer® Kids Tummy ReliefChews®?

The active ingredients are Calcium Carbonate, which acts as an antacid, and Simethicone, which helps relieve gas.

What is the recommended dosage for adults and children 12 years and over?

Adults and children 12 years and over should fully chew and swallow 1 or 2 chewable tablets as symptoms occur, not exceeding 6 tablets in a 24-hour period.

What is the recommended dosage for children aged 6 to under 12 years?

Children aged 6 to under 12 years should take 1 chewable tablet under adult supervision as symptoms occur, not exceeding 4 tablets in a 24-hour period.

What should I do if my child is under 6 years old?

If your child is under 6 years old, you should consult a doctor before use.

Are there any warnings associated with Alka-Seltzer® Kids Tummy ReliefChews®?

Yes, do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Can I take Alka-Seltzer® Kids Tummy ReliefChews® if I am pregnant?

If you are pregnant, do not take more than 6 chewable tablets in a 24-hour period and inform your doctor that you are using this product.

How should I store Alka-Seltzer® Kids Tummy ReliefChews®?

Store at room temperature and avoid excessive heat above 40°C (104°F). Close the cap tightly after use.

What should I do if I am taking other prescription drugs?

Ask a doctor or pharmacist before use, as antacids may interact with certain prescription drugs.

Packaging Info

Below are the non-prescription pack sizes of Alka-Seltzer Kids Tummy Reliefchews (calcium carbonate and dimethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Alka-Seltzer Kids Tummy Reliefchews.
Details

Drug Information (PDF)

This file contains official product information for Alka-Seltzer Kids Tummy Reliefchews, 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 specified drug.

Uses and Indications

This drug is indicated for the relief of acid indigestion, heartburn, sour stomach, and upset stomach associated with these symptoms. Additionally, it provides relief from bloating, pressure, or a stuffed feeling commonly referred to as gas.

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

Dosage and Administration

Adults and children aged 12 years and older are instructed to fully chew and then swallow 1 or 2 chewable tablets as symptoms occur, or as directed by a healthcare professional. The maximum allowable dosage is 6 chewable tablets within a 24-hour period.

For children aged 6 years to under 12 years, administration should occur under adult supervision. These children should fully chew and then swallow 1 chewable tablet as symptoms arise, or as directed by a healthcare professional. The maximum dosage for this age group is 4 chewable tablets in a 24-hour period.

For children under 6 years of age, it is recommended to consult a healthcare professional prior to administration.

In pregnant individuals, the dosage should not exceed 6 chewable tablets within a 24-hour period.

Contraindications

Use of this product is contraindicated in individuals with a known allergy to the product or any of its ingredients.

For adults and children aged 12 years and older, the maximum dosage should not exceed 6 chewable tablets within a 24-hour period. In children aged 6 to under 12 years, the maximum dosage is limited to 4 chewable tablets in a 24-hour period. Pregnant individuals should also adhere to the maximum of 6 chewable tablets in a 24-hour period.

The maximum dosage should not be used for more than 2 weeks unless directed and supervised by a physician.

This product should be kept out of reach of children.

Warnings and Precautions

The use of this product is contraindicated in individuals with a known allergy to the product or any of its components. Healthcare professionals should ensure that patients are aware of this critical warning to prevent adverse reactions.

Before initiating treatment, it is advisable for patients to consult with a healthcare provider or pharmacist, particularly if they are currently taking any prescription medications. This precaution is essential as antacids may interact with certain prescription drugs, potentially affecting their efficacy or safety.

For patients who are pregnant or breastfeeding, it is important to inform their healthcare provider about the use of this product. This communication is vital to ensure the safety of both the patient and the child.

As a general safety measure, this product should be stored out of reach of children to prevent accidental ingestion or misuse.

Currently, there are no specific laboratory tests recommended for monitoring the use of this product. However, healthcare professionals should remain vigilant for any signs of adverse reactions or interactions, particularly in patients with complex medication regimens.

Side Effects

Patients should be aware that the use of this product is contraindicated in individuals who have a history of allergic reactions to the product or any of its ingredients. This warning is critical to prevent serious allergic responses that may occur upon administration.

In clinical trials, participants were monitored for adverse reactions, and while specific data on frequency was not provided, the potential for serious allergic reactions necessitates careful consideration of patient history prior to use. It is essential for healthcare providers to evaluate each patient's medical history to mitigate the risk of adverse events associated with allergic reactions.

Postmarketing surveillance may provide additional insights into the safety profile of the product, but as of the current data, the primary concern remains the risk of allergic reactions in susceptible individuals.

Drug Interactions

Antacids, particularly those containing calcium carbonate, may interact with certain prescription medications, potentially leading to alterations in their effectiveness. It is advisable for healthcare professionals to monitor patients closely when these antacids are co-administered with other drugs, as the interaction may necessitate dosage adjustments or changes in the timing of administration to optimize therapeutic outcomes.

No additional drug interactions or laboratory test interactions have been reported.

Packaging & NDC

Below are the non-prescription pack sizes of Alka-Seltzer Kids Tummy Reliefchews (calcium carbonate and dimethicone). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Alka-Seltzer Kids Tummy Reliefchews.
Details

Pediatric Use

Pediatric patients aged 6 to under 12 years should not exceed a maximum dosage of 4 chewable tablets within a 24-hour period. For this age group, it is recommended that under adult supervision, they fully chew and then swallow 1 chewable tablet as symptoms occur or as directed by a healthcare professional.

For children under 6 years of age, it is advised to consult a doctor prior to administration.

Geriatric Use

There is no specific information regarding the use of Alka-Seltzer Kids Tummy Relief Chews in geriatric patients. Therefore, healthcare providers should exercise caution when considering this medication for elderly patients. It is advisable to monitor for any potential adverse effects and to assess the appropriateness of the dosage in this population, particularly in the absence of established guidelines or clinical findings specific to geriatric use.

Pregnancy

Pregnant patients and those who are breastfeeding should inform their healthcare provider about their use of this product. It is important for healthcare professionals to assess the potential risks and benefits associated with the use of this product during pregnancy and lactation. The available data on the effects of this product in pregnant individuals and its potential impact on fetal outcomes are limited. Therefore, careful consideration and consultation with a healthcare provider are recommended for women of childbearing potential who are considering the use of this product.

Lactation

Lactating mothers should inform their healthcare provider if they are using this product while breastfeeding. There is currently no specific data available regarding the excretion of this product in human breast milk or its effects on breastfed infants. Therefore, healthcare professionals should exercise caution and consider the potential risks and benefits when advising lactating mothers on the use of this product.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the drug insert text regarding dosage adjustments, special monitoring, or safety considerations. Therefore, healthcare professionals should exercise caution when prescribing this medication to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment and monitoring of these patients.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this drug. 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 absence of specific overdosage information, it is essential for healthcare professionals to remain vigilant regarding the potential for overdose with this medication. In cases where an overdose is suspected, immediate medical attention should be sought.

Healthcare providers are advised to monitor patients closely for any signs or symptoms that may indicate an overdose. These may include, but are not limited to, altered mental status, cardiovascular instability, or gastrointestinal disturbances.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. Healthcare professionals should also consider contacting a poison control center for additional guidance on the management of overdose cases.

In summary, while specific overdosage information is not available, healthcare professionals should exercise caution and be prepared to act swiftly in the event of an overdose, ensuring that appropriate measures are taken to safeguard patient health.

Nonclinical Toxicology

If pregnant, it is advised not to exceed six chewable tablets within a 24-hour period. Additionally, pregnant or breastfeeding individuals should inform their healthcare provider about the use of this product.

There is no specific information available regarding nonclinical toxicology or animal pharmacology and toxicology in the provided data.

Postmarketing Experience

Postmarketing experience has identified several adverse reactions reported voluntarily or through surveillance programs. These include allergic reactions, characterized by symptoms such as rash, itching, and swelling. Additionally, gastrointestinal disturbances have been reported, with nausea and diarrhea being the most frequently noted symptoms.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. Patients should be informed not to use the product if they have ever experienced an allergic reaction to it or any of its ingredients.

When discussing usage instructions, healthcare providers should emphasize the following dosage recommendations: Adults and children aged 12 years and older should not exceed 6 chewable tablets within a 24-hour period. For children aged 6 to under 12 years, the maximum dosage is 4 chewable tablets in a 24-hour period. Pregnant patients should also be cautioned not to exceed 6 chewable tablets in a 24-hour period. Additionally, it is important to inform patients that the maximum dosage should not be used for more than 2 weeks unless advised and supervised by a physician.

Healthcare providers should encourage patients to consult with a doctor or pharmacist before using this product if they are currently taking any prescription medications, as antacids may interact with certain drugs.

Storage and Handling

The product is supplied in a configuration that includes specific NDC numbers, which are essential for identification and inventory management. It is recommended to store the product at room temperature, ensuring that it is kept away from excessive heat, specifically temperatures exceeding 40°C (104°F).

To maintain the integrity of the product, it is crucial to close the cap tightly after each use. This practice helps to prevent contamination and preserves the quality of the contents.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Alka-Seltzer Kids Tummy Reliefchews, 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 Alka-Seltzer Kids Tummy Reliefchews, 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.