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Publix Ultra Strength

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Active ingredient
Calcium Carbonate 1000 mg
Other brand names
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2019
Label revision date
October 28, 2025
Active ingredient
Calcium Carbonate 1000 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 2019
Label revision date
October 28, 2025
Manufacturer
PUBLIX SUPER MARKETS, INC
Registration number
M001
NDC root
41415-103

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Drug Overview

Publix Ultra Strength is a chewable tablet that contains 1000 mg of calcium carbonate, which is an active ingredient known for its ability to relieve heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms. These tablets come in an assorted fruit flavor and are gluten-free, making them a convenient option for those seeking relief from digestive discomfort.

This product is distributed by Publix Super Markets and is comparable to Tums® Ultra Strength, although it is not manufactured by the same company. With 72 chewable tablets in each package, Publix Ultra Strength aims to provide effective relief for your stomach-related issues.

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 more comfortable and get back to your daily activities without the nagging discomfort of these digestive problems.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you should chew 2 to 3 tablets when you experience symptoms, or follow your doctor's instructions. It's important to remember that you should not swallow the tablets whole; they need to be chewed for the medication to work effectively.

Additionally, if your symptoms last longer than 2 weeks, you should consult with your doctor before continuing to take the medication. This ensures that you receive the appropriate care and guidance for your health.

What to Avoid

There are no specific contraindications, controlled substance classifications, or risks of abuse, misuse, or dependence associated with this medication. This means that, based on the available information, there are no particular situations or conditions under which you should avoid using it. Always consult with your healthcare provider for personalized advice and to ensure that this medication is appropriate for your individual health needs.

Side Effects

You may experience some side effects when using this product. It's important to be aware that taking more than 7 tablets in a 24-hour period can lead to adverse reactions. If you are pregnant, limit your intake to no more than 5 tablets in 24 hours. Additionally, using the maximum dosage for more than 2 weeks should only be done under the guidance of a doctor.

Before using this product, consult with your doctor or pharmacist, especially if you are currently taking any prescription medications, as antacids can interact with certain drugs. Always prioritize your health and safety by following these guidelines.

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 7 tablets in a 24-hour period, and if you are pregnant, limit your intake to no more than 5 tablets in 24 hours. 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, it's best to stop taking it and reach out to your healthcare provider for guidance. Always prioritize your health and safety by following these recommendations.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's important to be aware of the general signs of an overdose, which can include symptoms like extreme 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, you should contact your local emergency services or go to the nearest hospital right away. Always keep the medication packaging on hand, as it can provide important information to healthcare professionals. Remember, when in doubt, it’s better to err on the side of caution and seek help.

Pregnancy Use

If you are pregnant, it is important to be cautious with your medication. You should not take more than 5 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 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

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 use is to chew 2-3 tablets when symptoms occur, or as directed by a doctor. Please remember that the tablets should not be swallowed whole; they need to be chewed to be effective. Always consult with a healthcare professional if you have any questions about using this medication for your child.

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 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 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, 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. Currently, there are no specific drug interactions or laboratory test interactions noted for this medication. However, every individual is different, and your healthcare provider can help ensure that your treatment is safe and effective based on your unique health needs. Always feel free to ask questions and share all the medications and supplements you are using to avoid any potential issues.

Storage and Handling

To ensure the best performance and safety of your product, store it at room temperature. It's important to keep the container tightly closed to protect its contents. Before using, check that the safety seal (a printed seal under the cap) is intact; do not use the product if this seal is torn or missing, as this could indicate that the product is compromised. Following these 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 Publix Ultra Strength?

Publix Ultra Strength is a chewable antacid that contains 1000 mg of Calcium Carbonate and is available in assorted fruit flavors.

What symptoms does Publix Ultra Strength relieve?

It relieves heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms.

How should I take Publix 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 swallow the tablets whole.

Are there any warnings for using Publix Ultra Strength?

Yes, do not take more than 7 tablets in 24 hours, and if pregnant, do not take more than 5 tablets in 24 hours. Consult a doctor if you are taking prescription drugs.

Is Publix Ultra Strength safe to use during pregnancy?

While there are no teratogenic effects mentioned, pregnant women should not exceed 5 tablets in 24 hours.

What should I do if my symptoms persist?

Do not use Publix Ultra Strength for more than 2 weeks unless advised by a doctor.

Where can I find more information about Publix Ultra Strength?

You can contact Publix Super Markets, Inc. at 1-888-267-3037 for more information.

How should I store Publix Ultra Strength?

Store at room temperature and keep the container tightly closed. Do not use if the printed seal under the cap is torn or missing.

Packaging Info

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

Packaging configurations for Publix Ultra Strength.
Details

Drug Information (PDF)

This file contains official product information for Publix Ultra Strength, 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 effective in alleviating 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 3 tablets as symptoms occur, or as directed by a healthcare professional. It is important that the tablets are not swallowed whole.

Patients should not use this medication for symptoms that persist for more than 2 weeks without consulting a doctor.

Contraindications

There are no contraindications associated with the use of this product. It is not classified as a controlled substance, and there are no known risks of abuse, misuse, or dependence. Additionally, there are no specific instructions indicating that the product should not be taken or used under any circumstances.

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 7 tablets within a 24-hour period. For pregnant individuals, the maximum dosage should not exceed 5 tablets in a 24-hour period. Furthermore, the maximum dosage should not be utilized for more than 2 weeks unless under the guidance and supervision of a healthcare provider.

No specific general precautions or laboratory tests are required for the safe use of this product. However, it is essential for healthcare professionals to remain vigilant regarding potential interactions with other medications and to monitor patients for adherence to the recommended dosage guidelines.

Side Effects

Patients may experience various adverse reactions when using this product. It is important to note that certain warnings should be heeded prior to use. Patients are advised to consult a doctor or pharmacist if they are currently taking a prescription drug, as antacids may interact with specific medications.

When using this product, patients should adhere to the recommended dosage guidelines. Specifically, they should not exceed 7 tablets within a 24-hour period. For pregnant individuals, the maximum dosage should not exceed 5 tablets in a 24-hour period. Additionally, the maximum dosage should not be used for more than 2 weeks unless under the advice and supervision of a healthcare professional.

These precautions are essential to minimize the risk of adverse reactions and ensure safe use of the product.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there is no information available regarding 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 Publix Ultra Strength (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Publix Ultra Strength.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. For those aged 12 years and older, the recommended dosage is to chew 2-3 tablets as symptoms occur or as directed by a healthcare professional. It is important to note that tablets should not be swallowed whole.

Geriatric Use

There is no specific information available 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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

Pregnancy

Pregnant patients should not exceed a dosage of 5 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 recommendation during pregnancy 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 by lactating mothers. Additionally, there is no information available about the potential for excretion in breast milk or any associated risks to breastfed infants.

Renal Impairment

There is no specific information available regarding dosage adjustments, special monitoring, or safety considerations for patients with renal impairment. Healthcare professionals should exercise caution when prescribing to patients with reduced kidney function, as the absence of detailed guidance necessitates careful clinical judgment. Regular monitoring of renal function may be advisable in 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 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

There is currently no specific information available regarding overdosage for this medication. In the absence of documented overdosage data, healthcare professionals are advised to exercise caution and monitor patients closely for any unusual symptoms or adverse effects that may arise following administration.

In the event of suspected overdosage, it is recommended that healthcare providers initiate supportive care and symptomatic treatment as necessary. Monitoring of vital signs and laboratory parameters may be warranted to assess the patient's condition and guide further management.

Healthcare professionals should remain vigilant for potential symptoms that could indicate an overdosage scenario, although specific symptoms have not been detailed. If any adverse reactions or unexpected clinical presentations occur, appropriate medical intervention should be sought immediately.

For further guidance, healthcare providers are encouraged to consult local poison control centers or relevant medical authorities to obtain the most current recommendations for managing suspected overdosage cases.

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 use of the compound in these contexts.

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep the medication out of reach of children to prevent accidental ingestion or misuse. It is important for patients to understand the potential risks associated with improper access to the medication by young children. Providers should encourage patients to store the medication in a secure location and to be vigilant about monitoring its use.

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. Users are advised to check the safety seal; the product should not be used if the printed seal under the cap is torn or missing.

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 Publix Ultra Strength, 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 Publix Ultra Strength, 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.