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Ultra Strength

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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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2020
Label revision date
October 29, 2025
Drug Information (PDF)
Prescribing information, PDF file
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
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2020
Label revision date
October 29, 2025
Manufacturer
BETTER LIVING BRANDS LLC
Registration number
M001
NDC root
21130-302
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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

Ultra Strength Antacid is a type of antacid tablet that contains 1000 mg of calcium carbonate. It is designed to provide fast relief from common digestive discomforts such as heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms.

These tablets come in assorted berry flavors and are gluten-free, making them a convenient option for those seeking quick relief from digestive 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 confident using this medication, as there are no reported teratogenic effects (which means it doesn't cause birth defects) or nonteratogenic effects. This makes it a safe option for managing your digestive discomfort.

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 a doctor before continuing to take the medication. This ensures that you receive the appropriate care and guidance for your health.

What to Avoid

It's important to follow specific guidelines when using this medication to ensure your safety. Do not use the product if the printed seal under the cap is torn or missing, as this indicates it may not be safe to consume. You should not take more than 7 tablets in a 24-hour period, and if you are pregnant, limit your intake to no more than 5 tablets in the same timeframe. Additionally, avoid using the maximum dosage for more than 2 weeks unless your doctor has advised and is supervising you.

By adhering to these instructions, you can help prevent potential risks associated with misuse or overuse of the medication. Always consult with your healthcare provider if you have any questions or concerns about your treatment.

Side Effects

It's important to be aware of potential side effects when taking medication. If you are currently on a prescription drug, be cautious, as antacids can interact with certain medications, which may affect how well they work or increase the risk of side effects.

Always consult with your healthcare provider if you have concerns about interactions or if you experience any unusual symptoms while taking your medication. Your safety and well-being are paramount, so staying informed is key.

Warnings and Precautions

It's important to be aware of certain warnings and precautions when using this medication. If you are pregnant, do not take more than 5 tablets in a 24-hour period. Additionally, avoid using the maximum dosage for more than 2 weeks unless your doctor has advised and is supervising you.

You may need to undergo laboratory tests to monitor your health while using this medication. If you experience any severe side effects or unusual symptoms, seek emergency medical help immediately. Always consult your doctor if you have concerns or if you need to stop taking the medication for any reason.

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 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, contact your local emergency services or go to the nearest hospital right away. Having the medication packaging or details 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, it’s important to be cautious with medication. You should not take more than 5 tablets in a 24-hour period. Additionally, avoid using the maximum dosage for more than 2 weeks unless your doctor has advised and is supervising you. Always consult with your healthcare provider before taking any medication during pregnancy to ensure the safety of you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to be aware that there is no specific information available regarding the use of this medication during nursing. This means that the effects on breast milk and your baby are not clearly defined.

As always, it's best to consult with your healthcare provider about any medications you are considering while breastfeeding. They can help you weigh the potential risks and benefits to ensure the safety of both you and your baby.

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

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 wise to discuss any potential risks or benefits with a healthcare provider. They can help determine the best course of action based on individual health needs and any other medications being taken.

Always keep in mind that older adults may have different responses to medications, so regular monitoring and open communication with your healthcare team are essential for safety and effectiveness.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. Specifically, if you have reduced creatinine clearance (a measure of how well your kidneys are filtering waste), you should be closely monitored by your healthcare provider.

Before starting treatment, your renal function will be tested, and these tests should continue periodically throughout your treatment. If you have significant renal impairment, a lower dose of the medication is recommended to ensure your safety and effectiveness of the treatment. Always discuss any concerns with your doctor to ensure the best care for your kidney health.

Hepatic Impairment

If you have liver problems, it's important to know that your condition may affect how your body processes certain medications. This means that the dosage of the drug you are prescribed might need to be adjusted to ensure it is safe and effective for you.

Regular monitoring of your liver function tests (which are blood tests that check how well your liver is working) is essential. Additionally, special precautions should be taken when prescribing medications to you, so always discuss your liver health with your healthcare provider to ensure the best care.

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 share your complete list of medications and any recent lab tests to avoid any potential issues. Your health and safety should always come first.

Storage and Handling

To ensure the best performance of your product, store it at room temperature. It's important to keep the container tightly closed when not in use to protect the contents from contamination and maintain their effectiveness. By following these simple storage guidelines, you can help ensure the product remains safe and ready for use whenever you need it.

Additional Information

For adults and children aged 12 and older, you should chew 2-3 tablets when symptoms occur, or follow your doctor's instructions. It's important not to swallow the tablets whole. There is no additional information available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is Ultra Strength Antacid?

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

How should I take Ultra Strength Antacid?

Adults and children 12 years and older should chew 2-3 tablets as symptoms occur, or as directed by a doctor. Do not swallow the tablets whole.

What is the maximum dosage for Ultra Strength Antacid?

Do not take more than 7 tablets in 24 hours, and if pregnant, do not take more than 5 tablets in 24 hours.

Can I use Ultra Strength Antacid for more than 2 weeks?

You should not use the maximum dosage for more than 2 weeks unless advised and supervised by a doctor.

Are there any teratogenic effects associated with Ultra Strength Antacid?

No teratogenic effects are mentioned for Ultra Strength Antacid.

What should I do if the seal under the cap is torn or missing?

Do not use Ultra Strength Antacid if the printed seal under the cap is torn or missing.

What flavors does Ultra Strength Antacid come in?

Ultra Strength Antacid is available in assorted berry flavors and is both naturally and artificially flavored.

Is Ultra Strength Antacid gluten-free?

Yes, Ultra Strength Antacid is gluten-free.

What should I do if I am taking prescription drugs?

Antacids may interact with certain prescription drugs, so consult your doctor if you are currently taking any.

How should I store Ultra Strength Antacid?

Store Ultra Strength Antacid at room temperature and keep the container tightly closed.

Packaging Info

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

Packaging configurations for Ultra Strength.
Details

Drug Information (PDF)

This file contains official product information for 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 specified drug.

Uses and Indications

This drug is indicated for the relief of heartburn, acid indigestion, sour stomach, and 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 refrain from using this medication for symptoms that persist for more than 2 weeks unless advised by a healthcare provider.

Contraindications

Use is contraindicated in the following situations:

  • The product should not be used if the printed seal under the cap is torn or missing, as this may indicate tampering or contamination.

  • Patients should not exceed a dosage of 7 tablets within a 24-hour period to avoid potential adverse effects.

  • Pregnant individuals should limit their intake to a maximum of 5 tablets in a 24-hour period to mitigate risks to fetal health.

  • The maximum dosage should not be used for more than 2 weeks unless under the advice and supervision of a healthcare professional, to prevent potential complications associated with prolonged high-dose use.

Warnings and Precautions

Healthcare professionals should be aware of the following warnings and precautions associated with the use of this medication.

Warnings It is imperative to adhere to the recommended dosage guidelines to avoid potential adverse effects.

General Precautions Patients should be advised against exceeding a maximum dosage of five tablets within a 24-hour period if pregnant. Additionally, the maximum dosage should not be utilized for more than two weeks unless under the direct supervision and advice of a healthcare provider.

Laboratory Tests Regular monitoring may be necessary to ensure patient safety and medication efficacy. Healthcare professionals should consider appropriate laboratory tests as part of the patient management plan.

Get Emergency Medical Help In the event of severe side effects or an allergic reaction, immediate medical assistance should be sought.

Stop Taking and Call Your Doctor Patients must be instructed to discontinue use and consult their healthcare provider if they experience any concerning symptoms or if they are pregnant and have exceeded the recommended dosage.

Side Effects

Patients should be aware of potential adverse reactions associated with the use of this medication. While specific serious adverse reactions are not detailed, it is important to note that interactions may occur with other medications. For instance, antacids have the potential to interact with certain prescription drugs, which could affect the efficacy and safety of the treatment regimen.

In clinical practice, healthcare providers should monitor patients for any signs of adverse reactions, particularly in those who are concurrently taking prescription medications. It is advisable for patients to inform their healthcare provider of all medications they are currently using to mitigate the risk of interactions.

Overall, while the specific adverse reactions are not enumerated, the possibility of drug interactions underscores the importance of careful medication management in patients receiving this treatment.

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 Ultra Strength (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Ultra Strength.
Details

Pediatric Use

Pediatric patients should be kept 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, given the lack of targeted data for this population.

Pregnancy

Pregnant patients should not exceed a dosage of 5 tablets within a 24-hour period. It is advised that the maximum dosage not be used for more than 2 weeks unless under the guidance and supervision of a healthcare professional. The potential risks associated with exceeding these recommendations during pregnancy have not been fully characterized, and caution is warranted to avoid any adverse fetal outcomes. Healthcare providers should carefully evaluate the benefits and risks when prescribing this medication to pregnant patients.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or any lactation considerations. Healthcare professionals should exercise caution and consider the potential risks and benefits when prescribing this medication to lactating mothers. Further research may be necessary to fully understand the implications for breastfed infants.

Renal Impairment

Renal impairment may necessitate dosage adjustments for patients receiving treatment. It is essential that patients with reduced creatinine clearance are closely monitored to ensure safety and efficacy. Renal function tests should be performed prior to the initiation of therapy and periodically during treatment to assess any changes in renal status. For patients with significant renal impairment, a reduced dose is recommended to mitigate the risk of adverse effects associated with decreased kidney function.

Hepatic Impairment

Patients with hepatic impairment may experience altered metabolism of the drug, necessitating dosage adjustments to ensure safety and efficacy. It is essential to monitor liver function tests regularly in this population to assess the extent of hepatic impairment and guide treatment decisions. Special precautions should be taken when prescribing to patients with compromised liver function, as their response to the drug may differ from that of patients with normal liver function.

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 arise from an overdose. Common symptoms may include, but are not limited to, severe drowsiness, confusion, respiratory distress, or any unusual physiological changes.

Management of an overdose should be tailored to the individual patient and may involve supportive care, symptomatic treatment, and, if applicable, the use of specific antidotes. It is crucial to consult local poison control guidelines and follow established protocols for overdose management.

In all instances of suspected overdose, healthcare professionals should report the event to the appropriate regulatory authorities and document the incident thoroughly in the patient's medical record.

Nonclinical Toxicology

No information is available regarding teratogenic or non-teratogenic effects. Additionally, there is no data provided concerning nonclinical toxicology, animal pharmacology, or toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Patients should be advised to keep this product out of reach of children to prevent accidental ingestion. It is crucial to inform patients that they should not use the product if the printed seal under the cap is torn or missing, as this may indicate tampering.

When using this product, patients must be instructed not to exceed a dosage of 7 tablets within a 24-hour period. For pregnant patients, it is important to limit the intake to no more than 5 tablets in a 24-hour period. Additionally, patients should be cautioned against using the maximum dosage for more than 2 weeks unless advised and supervised by a healthcare professional.

Patients should also be encouraged to consult with their doctor or pharmacist prior to use if they are currently taking any prescription medications, as antacids may interact with certain prescription drugs. This precaution is essential to ensure safe and effective use of the product.

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 stability and efficacy.

Additional Clinical Information

For adults and children aged 12 years and over, the recommended administration involves chewing 2-3 tablets as symptoms occur or as directed by a healthcare professional. It is important to note that the tablets should not be swallowed whole.

No additional information is available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for 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 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.

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.