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Up and up Extra Strength Antacid 750

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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)
Marketed in the U.S.
Since 2015
Label revision date
November 4, 2025
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
Marketed in the U.S.
Since 2015
Label revision date
November 4, 2025
Manufacturer
Target Corporation
Registration number
M001
NDC root
11673-902

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Drug Overview

Calcium carbonate is an extra strength antacid that helps relieve common digestive discomforts. If you experience heartburn, acid indigestion, sour stomach, or an upset stomach associated with these symptoms, calcium carbonate can provide quick relief.

This medication comes in chewable tablet form, making it easy to take, and is available in an assorted berry flavor. It is also gluten-free, ensuring that it can be consumed by those with gluten sensitivities.

Uses

If you're experiencing discomfort from heartburn, acid indigestion, or a sour stomach, this medication can help relieve those symptoms. It is also effective for soothing an upset stomach that may be associated with these issues.

You can feel confident using this medication, as there are no known teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects reported.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can take 2 to 4 tablets by chewing them when you experience symptoms, or as your doctor recommends. It's important to follow this guidance closely to ensure you are using the medication safely and effectively.

However, if your symptoms last longer than 2 weeks, you should not continue taking the medication without consulting your doctor. This is crucial to avoid any potential complications and to ensure you receive the appropriate care. Always prioritize your health and seek professional advice when needed.

What to Avoid

You can feel reassured that there are no specific contraindications, controlled substance classifications, or risks of abuse or misuse associated with this medication. Additionally, there are no concerns regarding dependence (a condition where the body becomes reliant on a substance).

Since there are no explicit "do not take" or "do not use" instructions, it is important to follow your healthcare provider's guidance and discuss any concerns you may have about this medication. Always prioritize open communication with your healthcare team to ensure safe and effective use.

Side Effects

You may experience some side effects when using this product. Common reactions include stomach upset, constipation, or diarrhea. It's important to be aware that taking more than the recommended dosage can lead to more serious issues. For instance, do not exceed 10 tablets in a 24-hour period, and if you are pregnant, limit your intake to 6 tablets in the same timeframe.

Additionally, if you are currently taking any prescription medications, consult with your doctor or pharmacist before using this product, as it may interact with certain drugs. Avoid using the maximum dosage for more than two weeks unless directed by a healthcare professional.

Warnings and Precautions

Before using this product, it's important to consult with your doctor or pharmacist, especially if you are currently taking any prescription medications, as antacids can interact with them. Be mindful of the dosage: do not exceed 10 tablets in a 24-hour period, and if you are pregnant, limit your intake to no more than 6 tablets in that same timeframe. Additionally, avoid using the maximum dosage for more than 2 weeks unless directed by your doctor.

If you experience any unusual symptoms or have concerns while using this product, stop taking it and reach out to your doctor for guidance. Always prioritize your health and safety by following these recommendations closely.

Overdose

If you suspect an overdose, it's important to act quickly. Signs of an overdose can vary, but they may include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms, seek immediate medical help.

In the event of an overdose, contact your local emergency services or go to the nearest hospital. It's always better to be safe and get professional assistance if you have concerns about your health. Remember, timely action can make a significant difference.

Pregnancy Use

If you are pregnant, it is important to be cautious with medication. You should not take more than 6 tablets in a 24-hour period. Always consult with your healthcare provider before taking any medication to ensure it is safe for you and your baby. Your health and the health of your developing child are the top priority, so make sure to follow these guidelines closely.

Lactation Use

If you are breastfeeding, you can feel reassured that there are no specific warnings or recommendations regarding the use of this product while nursing. Additionally, there is no information available about whether this product is excreted in breast milk or any potential risks to your infant. Always consult with your healthcare provider if you have any concerns or questions about medications while breastfeeding.

Pediatric Use

If you are considering this medication for your child, it's important to note that it is intended for use in children aged 12 years and older. For this age group, the recommended dosage is to chew 2 to 4 tablets when symptoms arise, or as directed by a healthcare professional. Always consult with your child's doctor before starting any new medication to ensure it is appropriate for their specific needs.

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 healthcare providers may not have tailored guidelines for elderly patients.

If you or a loved one is an older adult considering this medication, it’s important to discuss any potential risks and benefits with your healthcare provider. They can help determine the best approach based on individual health needs and circumstances. Always prioritize open communication with your doctor 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 related to 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 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 or tests you may be taking. While there are no specific drug interactions or laboratory test interactions noted for this medication, your healthcare provider can help ensure that everything you are taking works well together and is safe for you.

Always feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

Storage and Handling

To ensure the best performance and safety of your product, store it in a cool, dry place at temperatures below 30°C (86°F). This helps maintain its effectiveness. Before using, always check that the safety seal under the cap is intact; do not use the product if the seal is torn or missing, as this could indicate contamination or that the product is no longer safe to use.

By following these simple storage and handling guidelines, you can help ensure that your product remains safe and effective for your needs.

Additional Information

You should 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 calcium carbonate?

Calcium carbonate is an extra strength antacid that relieves heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms.

How should I take calcium carbonate?

Adults and children 12 years of age and over should chew 2-4 tablets as symptoms occur, or as directed by a doctor.

Are there any warnings I should be aware of?

Yes, do not take more than 10 tablets in 24 hours, and if pregnant, do not take more than 6 tablets in 24 hours. Consult a doctor if you are taking prescription drugs, as antacids may interact with them.

Can I use calcium carbonate if I am pregnant?

If you are pregnant, do not take more than 6 tablets in 24 hours and consult your doctor for advice.

Are there any side effects associated with calcium carbonate?

The insert does not list any specific side effects, but you should stop taking it and consult your doctor if you experience any unusual symptoms.

Is calcium carbonate gluten-free?

Yes, calcium carbonate is gluten-free.

What should I do if my symptoms persist?

Do not take calcium carbonate for symptoms that persist for more than 2 weeks unless advised by a doctor.

How should I store calcium carbonate?

Store calcium carbonate below 30°C (86°F) and ensure the safety seal under the cap is intact.

Packaging Info

Below are the non-prescription pack sizes of Up and up Extra Strength Antacid 750 (antacid tablets). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Up and up Extra Strength Antacid 750.
Details

Drug Information (PDF)

This file contains official product information for Up and up Extra Strength Antacid 750, 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 drug.

Uses and Indications

This drug is indicated for the relief of heartburn, acid indigestion, and sour stomach. It is also indicated for the relief of upset stomach associated with these symptoms.

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 chew 2 to 4 tablets as symptoms occur, or as directed by a healthcare professional. It is important to note that this medication should not be taken for symptoms that persist for more than 2 weeks unless advised by a doctor.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

It is imperative that healthcare professionals advise patients to consult a doctor or pharmacist prior to using this product if they are currently taking any prescription medications, as antacids may interact with certain drugs.

When administering this product, it is crucial to adhere to the following dosage guidelines: patients should not exceed 10 tablets within a 24-hour period. For pregnant individuals, the maximum dosage should not exceed 6 tablets in a 24-hour timeframe. Furthermore, the maximum dosage should not be utilized for more than 2 weeks unless directed and monitored by a healthcare professional.

Currently, there are no specific general precautions or laboratory tests associated with the use of this product. However, it is essential for healthcare providers to remain vigilant and monitor patients for any adverse effects or interactions, particularly in those taking concurrent medications.

Side Effects

Patients may experience various adverse reactions when using this product. It is important to note that certain warnings should be heeded to minimize risks associated with its use.

Patients are advised to consult a doctor or pharmacist prior to use if they are currently taking any prescription medications, as antacids may interact with specific drugs. When using this product, patients should not exceed a dosage of 10 tablets within a 24-hour period. For pregnant individuals, the maximum recommended dosage is limited to 6 tablets in a 24-hour timeframe. Furthermore, patients should refrain from using the maximum dosage for more than 2 weeks unless under the guidance and supervision of a healthcare professional.

These precautions are essential to ensure the safe use of the product and to mitigate potential adverse reactions.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known interactions with laboratory tests. As such, no specific recommendations for dosage adjustments or monitoring are warranted at this time.

Packaging & NDC

Below are the non-prescription pack sizes of Up and up Extra Strength Antacid 750 (antacid tablets). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Up and up Extra Strength Antacid 750.
Details

Pediatric Use

Pediatric patients aged 12 years and older may chew 2-4 tablets as symptoms occur, or as directed by a healthcare professional. There are no specific dosage adjustments or safety concerns noted for this age group. Further studies may be warranted to evaluate efficacy and safety in younger populations.

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

Pregnant patients should not exceed a dosage of 6 tablets within a 24-hour period. This limitation is crucial to minimize potential risks to fetal outcomes. Healthcare professionals are advised to counsel women of childbearing potential regarding the importance of adhering to this dosage guideline to ensure the safety of both the mother and the developing fetus.

Lactation

There are no specific warnings or recommendations regarding the use of this product in nursing mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

Patients with renal impairment have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

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 overdosage information, it is essential for healthcare professionals to remain vigilant and consider general principles of management in cases of suspected overdose.

Healthcare providers should be aware that the clinical presentation of an overdose may vary depending on the substance involved and the individual patient’s characteristics. Symptoms may include, but are not limited to, altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of an overdose, immediate assessment of the patient's condition is crucial. Recommended actions include:

  1. Assessment and Monitoring: Conduct a thorough evaluation of the patient's vital signs and level of consciousness. Continuous monitoring may be necessary to detect any changes in the patient's status.

  2. Supportive Care: Provide supportive care as needed, which may involve airway management, oxygen supplementation, intravenous fluids, and other interventions to stabilize the patient.

  3. Decontamination: If the overdose is recent and the patient is alert and able to protect their airway, consider gastrointestinal decontamination methods such as activated charcoal, following established protocols.

  4. Consultation with Poison Control: Engage with a poison control center for guidance on specific management strategies tailored to the substance involved in the overdose.

  5. Symptomatic Treatment: Address any specific symptoms that arise, utilizing appropriate pharmacological interventions as indicated.

  6. Hospitalization: Depending on the severity of the overdose and the patient's response to initial management, hospitalization may be warranted for further observation and treatment.

In summary, while specific overdosage information is not provided, healthcare professionals should apply general overdose management principles and remain prepared to respond effectively to any potential overdose situation.

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 provided in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage to ensure the safety of young individuals.

Storage and Handling

The product is supplied in a safety-sealed container. It is imperative that the product is not used if the printed seal under the cap is torn or missing.

For optimal storage, the product should be kept at temperatures below 30°C (86°F) to ensure its integrity and efficacy. Proper handling and storage conditions are essential to maintain the quality of the product throughout its shelf life.

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 Up and up Extra Strength Antacid 750, 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 Antacid 750, 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.