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Goodsense Extra Strength Antacid

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Active ingredient
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 2024
Label revision date
September 13, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
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 2024
Label revision date
September 13, 2024
Manufacturer
GoodSense
Registration number
M001
NDC root
50804-151
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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If you are a consumer or patient please visit this version.

Drug Overview

GOOD SENSE® Extra Strength is an antacid that comes in chewable tablet form, containing 750 mg of calcium carbonate. It is designed to provide fast relief from heartburn, acid indigestion, and upset stomach, making it a helpful option for those experiencing discomfort related to excess stomach acid.

These tablets are available in tropical fruit flavors, making them a more pleasant option for relief. If you're looking for a product that can help alleviate these common digestive issues, GOOD SENSE® Extra Strength may be a suitable choice.

Uses

If you're experiencing discomfort from acid indigestion, heartburn, or an upset stomach, this medication can help provide relief. It works effectively to ease these common digestive issues, allowing you to feel more comfortable throughout your day.

You can trust that this medication does not have any known teratogenic effects, meaning it does not cause harm to a developing fetus. This makes it a safer option for those who may be pregnant or planning to become pregnant.

Dosage and Administration

When you need relief from your symptoms, start by wetting your mouth before chewing the tablets. For adults and children aged 12 and older, you can chew 2 to 4 tablets as needed, or follow your doctor's instructions for the right amount. Remember to take them only when symptoms arise to ensure you’re using the medication effectively.

What to Avoid

It's important to use this medication responsibly to ensure your safety. You should not take more than 10 tablets within a 24-hour period. Additionally, avoid using the maximum dosage for more than 2 weeks unless your doctor has advised you to do so. Following these guidelines will help prevent any potential issues related to misuse or overuse. Always consult with your healthcare provider if you have any questions or concerns about your medication.

Side Effects

It seems that there are no specific warnings or adverse reactions provided in the extracted facts. If you have any additional information or details about the side effects, please share them, and I would be happy to help you rewrite that information in a clear and consumer-friendly manner.

Warnings and Precautions

While there are no specific warnings or precautions listed for this medication, it's always important to stay informed about your health. If you experience any unusual symptoms or side effects while taking this medication, you should stop using it and consult your doctor for guidance.

Additionally, if you have any concerns or questions about your treatment, don't hesitate to reach out to your healthcare provider. They can provide you with the necessary information and support to ensure your safety and well-being.

Overdose

If you suspect an overdose of this medication, it's important to stay calm and take immediate action. While the drug insert does not provide specific information about overdose, 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 have concerns about an overdose, 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 professional assistance if you think something is wrong.

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

It's important to keep this medication out of reach of children to ensure their safety. For adults and children aged 12 years and older, the recommended dosage is to chew 2 to 4 tablets when symptoms occur, or as directed by a doctor.

If you have younger children, please consult with a healthcare professional for guidance, as this medication is not specifically recommended for them. Always prioritize safety and follow the advice of your doctor regarding any medication use.

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 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 for patients with 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 regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective care.

Drug Interactions

It's important to be aware that antacids, which are commonly used to relieve heartburn and indigestion, can interact with some prescription medications. This means that taking antacids at the same time as certain drugs may affect how well those medications work.

To ensure your safety and the effectiveness of your treatment, always discuss any medications you are taking, including over-the-counter products like antacids, with your healthcare provider. They can help you understand potential interactions and adjust your treatment plan if necessary.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool, dry place at temperatures below 30°C (86°F). This helps maintain its quality and performance.

Before using the product, check that the printed seal under the cap is intact. If the seal is torn or missing, do not use the product, as this may indicate that it has been compromised. Following these guidelines will help you use the product safely and effectively.

Additional Information

You should take this medication orally. For adults and children aged 12 and over, wet the tablets in your mouth before chewing, and chew 2 to 4 tablets as symptoms occur or as directed by your doctor.

Before using this medication, it's important to consult with your doctor or pharmacist if you are currently taking any prescription drugs, as antacids can interact with certain medications. Additionally, if you are pregnant or breastfeeding, seek advice from a healthcare professional before use.

FAQ

What is GOOD SENSE® Extra Strength?

GOOD SENSE® Extra Strength is an antacid that comes in chewable tablet form, containing 750mg of Calcium Carbonate.

What symptoms does GOOD SENSE® Extra Strength relieve?

It relieves heartburn, acid indigestion, and upset stomach.

How should I take GOOD SENSE® Extra Strength?

Adults and children 12 years and older should wet the tablet in their mouth before chewing and take 2-4 tablets as symptoms occur, or as directed by a doctor.

Are there any dosage restrictions for GOOD SENSE® Extra Strength?

Do not take more than 10 tablets in a 24-hour period or use the maximum dosage for more than 2 weeks without a doctor's advice.

Is GOOD SENSE® Extra Strength safe to use during pregnancy or breastfeeding?

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

What should I do if I have a prescription drug?

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

How should I store GOOD SENSE® Extra Strength?

Store it below 30°C (86°F) and do not use if the printed seal under the cap is torn or missing.

What flavors does GOOD SENSE® Extra Strength come in?

It is available in tropical fruit flavors.

Are there any contraindications for using GOOD SENSE® Extra Strength?

No specific contraindications are mentioned.

What is the quantity of GOOD SENSE® Extra Strength in a package?

Each package contains 96 chewable tablets.

Packaging Info

Below are the non-prescription pack sizes of Goodsense Extra Strength Antacid (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Goodsense Extra Strength Antacid.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

GOOD SENSE® Extra Strength Antacid Tablets contain 750 mg of Calcium Carbonate per tablet. These chewable tablets are formulated to provide fast relief from heartburn, acid indigestion, and upset stomach. The product is available in a tropical fruit flavor and is packaged in a bottle containing 96 tablets. The National Drug Code (NDC) for this product is 50804-151-22. This formulation is comparable to the active ingredient found in Extra Strength Tums®.

Uses and Indications

This drug is indicated for the relief of acid indigestion, heartburn, and upset stomach.

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

Dosage and Administration

For adults and children aged 12 years and over, the recommended administration involves wetting the mouth prior to chewing. Patients should chew 2 to 4 tablets as symptoms occur, or as directed by a healthcare professional. It is important to follow the prescribed dosage to ensure optimal efficacy and safety.

Contraindications

Use of this product is contraindicated in patients who exceed the recommended dosage of 10 tablets within a 24-hour period or utilize the maximum dosage for more than 2 weeks without the guidance and supervision of a healthcare professional. Adherence to these guidelines is essential to prevent potential adverse effects associated with excessive use.

Warnings and Precautions

There are currently no specific warnings or general precautions associated with the use of this medication. Healthcare professionals are advised to remain vigilant and monitor patients for any adverse effects or unusual symptoms that may arise during treatment.

Additionally, no laboratory tests have been specified for monitoring purposes in relation to this medication. It is essential for healthcare providers to use clinical judgment and consider individual patient circumstances when determining the need for any laboratory evaluations.

In the absence of explicit instructions regarding emergency medical assistance or directives to discontinue use and consult a physician, practitioners should maintain open communication with patients about any concerns or side effects they may experience. Regular follow-up and assessment are recommended to ensure patient safety and treatment efficacy.

Side Effects

There are currently no specific adverse reactions, warnings, or additional important notes provided for this medication. As such, no information regarding serious or common adverse reactions, clinical trial data, or postmarketing experiences is available at this time. It is essential for healthcare professionals to monitor patients for any potential adverse effects and report them as necessary. Further information may be obtained from future updates or clinical studies.

Drug Interactions

Antacids may interact with various prescription medications, potentially affecting their absorption and efficacy. It is advisable to separate the administration of antacids and other medications by at least two hours to minimize the risk of interaction. Monitoring for therapeutic effectiveness of the affected drugs is recommended when antacids are used concurrently.

Packaging & NDC

Below are the non-prescription pack sizes of Goodsense Extra Strength Antacid (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Goodsense Extra Strength Antacid.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. For children aged 12 years and older, the recommended dosage is to chew 2-4 tablets as symptoms occur, or as directed by a healthcare professional.

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 considered, 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 safe use during pregnancy and breastfeeding.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data regarding the excretion of this drug in human 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 not been specifically addressed in the available data 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 lack of information necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in these patients to ensure safety and efficacy.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to the use of 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 available information.

Overdosage

In the context of overdosage, it is important to note that the available sections of the drug insert do not provide specific information regarding potential overdosage scenarios.

Healthcare professionals are advised to remain vigilant and consider the possibility of overdosage in patients presenting with unusual symptoms or clinical deterioration. In the absence of detailed guidance, standard supportive care measures should be implemented.

Should an overdosage be suspected, it is recommended that healthcare providers monitor the patient closely for any adverse effects and manage symptoms as they arise. Supportive treatment may include maintaining airway patency, ensuring adequate ventilation, and providing cardiovascular support as necessary.

In cases of suspected overdosage, it is prudent to contact a poison control center or seek expert consultation for further management recommendations.

Nonclinical Toxicology

There is currently no available information regarding teratogenic effects. Additionally, no data has been provided concerning non-teratogenic effects. The nonclinical toxicology section does not contain any relevant information at this time. Furthermore, there is no information available related to animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients not to exceed a maximum of 10 tablets within a 24-hour period. Additionally, patients should be informed that the maximum dosage of this product should not be used for more than 2 weeks unless directed by a healthcare professional.

It is also important for healthcare providers to encourage patients to consult with a doctor or pharmacist prior to use if they are currently taking any prescription medications. This is crucial as antacids may interact with certain prescription drugs, potentially leading to adverse effects or reduced efficacy of the medications.

Storage and Handling

The product is supplied in a configuration that includes an NDC number for identification. It should be stored at temperatures below 30°C (86°F) to maintain its integrity and efficacy. Healthcare professionals are advised to inspect the product prior to use; it should not be used if the printed seal under the cap is torn or missing, as this may indicate potential tampering or contamination. Proper handling and storage conditions are essential to ensure the product remains safe and effective for patient use.

Additional Clinical Information

Patients aged 12 years and older are advised to take the medication orally by wetting it in the mouth before chewing 2-4 tablets as symptoms occur or as directed by a healthcare professional. Clinicians should counsel patients to consult a doctor or pharmacist prior to use if they are currently taking any prescription medications, as antacids may interact with certain drugs. Additionally, it is recommended that individuals who are pregnant or breastfeeding seek advice from a health professional before using the product.

Drug Information (PDF)

This file contains official product information for Goodsense Extra Strength Antacid, 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 Goodsense Extra Strength Antacid, 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.