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Goodsense Ultra Strength Antacid

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Active ingredient
Calcium Carbonate 1000 mg
Other brand names
Drug classes
Blood Coagulation Factor, Phosphate Binder
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2018
Label revision date
January 20, 2025
Active ingredient
Calcium Carbonate 1000 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
Marketed in the U.S.
Since 2018
Label revision date
January 20, 2025
Manufacturer
Good Sense (Geiss, Destin & Dunn, Inc.)
Registration number
M001
NDC root
50804-175

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Drug Overview

GOODSENSE Ultra Strength is an antacid medication that contains 1000 mg of calcium carbonate, which helps to neutralize stomach acid. You can use it to relieve symptoms such as acid indigestion, heartburn, and upset stomach. This product is designed to provide fast relief, making it a convenient option for managing these common digestive discomforts.

Available in assorted berry flavors, GOODSENSE Ultra Strength comes in a package of 72 chewable tablets, allowing you to easily take it when needed. It is comparable to the active ingredient found in Tums Ultra Strength, offering a familiar and effective solution for your digestive issues.

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 developmental problems in a fetus. This makes it a safer option for those who may be pregnant or planning to become pregnant.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can take this medication by chewing 2 to 3 tablets whenever you experience symptoms, or as your doctor advises. It's important to follow the recommended dosage to ensure the best results. Always consult with your healthcare provider if you have any questions about how to use this medication effectively.

What to Avoid

It's important to use this product safely to avoid potential issues. You should not take more than 7 tablets in a 24-hour period, and you should not use the maximum dosage for more than 2 weeks unless your doctor advises you to do so. Following these guidelines helps ensure your safety and well-being while using this medication. Always consult with your healthcare provider if you have any questions or concerns about your treatment.

Side Effects

You may experience some side effects when taking this medication. While no specific side effects are listed, it's important to be aware that antacids can interact with certain prescription drugs, which may affect how well those medications work.

If you have any concerns about potential interactions or side effects, it's a good idea to discuss them with your healthcare provider. They can provide you with more personalized information based on your health needs.

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 an overdose, such as unusual drowsiness, confusion, or difficulty breathing.

If you notice any of these symptoms, or if you are unsure whether an overdose has occurred, 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 advice in these situations.

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

When it comes to using this medication for children, it's important to note that it is not recommended for those under 12 years of age. For adults and children aged 12 and older, you should chew 2-3 tablets as symptoms arise, or follow your doctor's instructions.

Always remember to keep this medication out of reach of younger children to ensure their safety. If you have any concerns or questions about its use in your child, consult with a healthcare professional.

Geriatric Use

While there is no specific information available about the use of this medication in older adults, it’s important to approach any new treatment with caution. If you or a loved one is an older adult, it’s always a good idea to discuss any medications with a healthcare provider. They can help ensure that the treatment is safe and appropriate, considering any unique health needs or conditions that may be present.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider will be the best resource for personalized advice. Always keep them informed about any other medications or health issues to ensure safe and effective care.

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. To ensure your safety, your healthcare provider will monitor your kidney function regularly, especially by checking your creatinine clearance (a test that measures how well your kidneys are filtering waste).

Before starting any new treatment, your renal function should be tested, and these tests will continue periodically throughout your therapy. This way, your doctor can make any necessary dosage adjustments based on your kidney health. Always communicate with your healthcare team about your kidney function to ensure the best care.

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 determine the best approach for your treatment and monitor your liver function as needed.

Make sure to keep your doctor informed about your liver health, as they may want to conduct regular tests to ensure your safety while using any medication. Your well-being is a priority, and your healthcare team is there to support you.

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 could affect how well those medications work.

To ensure your safety and the effectiveness of your treatments, always discuss any medications, 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 at room temperature and keep the container tightly closed when not in use. This helps maintain its quality and prevents contamination.

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 simple guidelines will help you use the product safely and effectively.

Additional Information

You will take this medication orally. There are no additional details available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experiences. If you have any questions or concerns about your treatment, be sure to discuss them with your healthcare provider.

FAQ

What is GOODSENSE Ultra Strength?

GOODSENSE Ultra Strength is an antacid tablet containing 1000 mg of Calcium Carbonate, designed to relieve acid indigestion, heartburn, and upset stomach.

How should I take GOODSENSE Ultra Strength?

Adults and children 12 years of age and over should chew 2-3 tablets as symptoms occur, or as directed by a doctor. Do not take more than 7 tablets in a 24-hour period.

Are there any contraindications for using GOODSENSE Ultra Strength?

No specific contraindications are mentioned for GOODSENSE Ultra Strength.

Can I use GOODSENSE Ultra Strength if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, you should ask a health professional before using GOODSENSE Ultra Strength.

What should I do if I have renal impairment?

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

What flavors does GOODSENSE Ultra Strength come in?

GOODSENSE Ultra Strength is available in assorted berry flavors.

How should I store GOODSENSE Ultra Strength?

Store GOODSENSE Ultra Strength at room temperature, keep the container tightly closed, and do not use it if the printed seal under the cap is torn or missing.

Are there any known side effects of GOODSENSE Ultra Strength?

No specific side effects are listed for GOODSENSE Ultra Strength, but antacids may interact with certain prescription drugs.

Packaging Info

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

Packaging configurations for Goodsense Ultra Strength Antacid.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

GOODSENSE Ultra Strength is an antacid formulation available in chewable tablet form, designed to provide fast relief from heartburn, acid indigestion, and upset stomach. Each tablet contains 1000 mg of Calcium Carbonate as the active ingredient. The product is offered in assorted berry flavors and is packaged in a bottle containing 72 chewable tablets. The National Drug Code (NDC) for this product is 50804-175-68. This formulation is comparable to the active ingredient found in Tums Ultra 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

Adults and children 12 years of age and over are advised to chew 2 to 3 tablets as symptoms occur, or as directed by a healthcare professional. It is important to follow the recommended dosage and not exceed the advised amount unless specifically instructed by a physician.

Contraindications

Use of this product is contraindicated in patients who exceed the recommended dosage of more than 7 tablets within a 24-hour period or who utilize the maximum dosage for longer 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. Additionally, no laboratory tests have been identified as necessary for monitoring during treatment.

Healthcare professionals are advised to remain vigilant and assess the patient’s overall health status regularly. In the absence of specific emergency medical help instructions or directives to discontinue use and consult a physician, it is essential to maintain open communication with patients regarding any emerging symptoms or concerns. Regular follow-up appointments should be encouraged to ensure the safe and effective use of the medication.

Side Effects

Patients may experience various adverse reactions associated with the use of this medication. While no specific side effects are detailed in the warnings section, it is important to note that antacids can interact with certain prescription drugs, which may lead to altered efficacy or increased risk of adverse effects from those medications.

In clinical practice, healthcare providers should be vigilant in monitoring patients for any potential interactions and advise them accordingly. It is essential for patients to disclose all medications they are taking to their healthcare provider to mitigate the risk of adverse reactions related to drug interactions.

Drug Interactions

Antacids may interact with various prescription medications, potentially affecting their absorption and efficacy. It is advisable to monitor the timing of antacid administration in relation to other medications to minimize these interactions. Specifically, antacids should be taken at least 2 hours apart from other drugs to ensure optimal therapeutic outcomes.

Packaging & NDC

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

Packaging configurations for Goodsense Ultra Strength Antacid.
Details

Pediatric Use

Pediatric patients aged 12 years and older may use the medication as directed for symptom relief. The recommended dosage for this age group is to chew 2-3 tablets as symptoms occur or as directed by a healthcare professional.

It is important to keep the medication out of reach of younger children to prevent accidental ingestion.

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 they may have altered pharmacokinetics and pharmacodynamics. Close monitoring is recommended to ensure safety and efficacy in 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 breastfeeding infants are not fully established. It is essential for women of childbearing potential to discuss their individual circumstances with their healthcare provider to ensure safe use during pregnancy and lactation.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is no specific data available regarding the excretion of this medication in breast milk or its effects on breastfed infants. Therefore, caution is recommended when administering this medication to lactating mothers.

Renal Impairment

Patients with renal impairment may necessitate dosage adjustments based on their level of renal function. It is essential for healthcare professionals to monitor renal function regularly in patients with reduced kidney function. Dosage adjustments should be guided by creatinine clearance levels, ensuring that therapy is tailored to the patient's specific renal status. Additionally, renal function tests should be performed prior to initiating therapy and periodically thereafter to assess any changes in renal function that may impact dosing.

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 in the available sections of the drug insert, healthcare professionals are advised to exercise caution and consider general principles of management for suspected overdosage cases.

Recommended Actions In the event of an overdosage, it is essential for healthcare providers to assess the patient's clinical status and initiate appropriate supportive care. Monitoring of vital signs and symptomatic treatment should be prioritized.

Potential Symptoms While specific symptoms related to overdosage are not detailed, healthcare professionals should remain vigilant for any unusual or severe reactions that may arise, given the lack of documented information.

Management Procedures In the case of suspected overdosage, it is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for guidance on management strategies. Supportive measures, including the administration of activated charcoal if appropriate and the implementation of symptomatic treatment, may be necessary based on the clinical presentation of the patient.

Overall, due to the absence of detailed overdosage information, a cautious and individualized approach is warranted in managing potential cases.

Nonclinical Toxicology

There is currently no available information regarding teratogenic effects, non-teratogenic effects, or any specific findings in the nonclinical toxicology section. Additionally, there are no details provided concerning animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available for SPL code 90375-7.

Patient Counseling

Healthcare providers should advise patients not to exceed a maximum of 7 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 physician.

It is also important for healthcare providers to encourage patients to consult with a doctor or pharmacist prior to using this product if they are currently taking any prescription medications. Patients should be made aware that antacids may interact with certain prescription drugs, and this interaction could affect the efficacy of their treatment.

Storage and Handling

The product is supplied in a container that must be kept tightly closed to maintain its integrity. It should be stored at room temperature to ensure optimal conditions. Healthcare professionals are advised not to use the product if the printed seal under the cap is torn or missing, as this may indicate compromised quality or safety.

Additional Clinical Information

The medication is administered orally. There are no additional details available regarding laboratory tests, abuse information, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Goodsense Ultra 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 Ultra 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

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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.