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Ultra Strength Antacid Assorted Berries

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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 2025
Label revision date
February 4, 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 2025
Label revision date
February 4, 2025
Manufacturer
Retail Business Services, LLC.
Registration number
M001
NDC root
72476-178
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info
Packaging & NDC Codes

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

CAREOne™ is an ultra-strength calcium antacid that contains 1000 mg of calcium carbonate, which helps relieve symptoms of acid indigestion and heartburn. Available in a chewable tablet form with assorted berry flavors, this gluten-free product is designed to provide fast relief from discomfort caused by excess stomach acid.

If you're experiencing heartburn or acid indigestion, CAREOne™ may be a helpful option to consider for quick symptom relief.

Uses

If you're experiencing discomfort from acid indigestion or heartburn, this medication can help relieve those symptoms. Acid indigestion is often characterized by a burning sensation in your stomach or chest, while heartburn is the feeling of warmth or pain that can rise from your stomach to your throat.

You can use this medication to find relief from these common digestive issues, allowing you to feel more comfortable throughout your day. Rest assured, there are no known teratogenic effects (harmful effects on fetal development) associated with this medication, making it a safer option for those who may be 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, chew 2 to 3 tablets as your symptoms arise, or follow your doctor's instructions for the best results. Remember to only take the tablets when you need them, ensuring you’re using them safely and effectively.

What to Avoid

It's important to use this medication responsibly to ensure your safety. You should not take more than 7 tablets in a 24-hour period, and avoid using the maximum dosage for more than 2 weeks unless your doctor advises you otherwise. Following these guidelines helps prevent potential issues and ensures the medication works effectively for you. 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 or notice unusual symptoms, be sure to consult your healthcare provider for guidance.

Warnings and Precautions

It's important to use this medication safely. 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.

If you experience any unusual symptoms or have concerns about your health while using this medication, stop taking it and call your doctor for guidance. Always prioritize your health and safety by following these instructions closely.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there is no specific information available about the effects of an overdose for this medication, 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 if you believe you have taken too much of the medication, 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 checked out if you have concerns about an overdose.

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 intended for those aged 12 years and older. For both adults and children in this age group, the recommended dosage is to chew 2-3 tablets as symptoms arise or as directed by a healthcare professional.

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 your doctor for personalized advice.

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 for personalized advice. 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 your medication dosage may need to be adjusted. This adjustment is based on your creatinine clearance levels, which is a measure of how well your kidneys are filtering waste from your blood. To ensure your safety, your renal function should be monitored regularly, starting with tests before you begin treatment and continuing periodically throughout your therapy.

Regular monitoring helps your healthcare provider make informed decisions about your treatment plan. Always discuss any concerns with your doctor, as they can provide guidance tailored to your specific needs.

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 liver function tests (which check how well your liver is working) to ensure your safety while using any medication.

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 treatments, 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 best quality and safety of your product, store it at room temperature and keep the container tightly closed. This helps maintain its effectiveness and prevents contamination.

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

Additional Information

You should take this medication orally. For adults and children aged 12 and older, wet the tablets in your mouth before chewing, and chew 2-3 tablets as symptoms occur or as directed by your doctor. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling.

FAQ

What is CAREOne™?

CAREOne™ is an ultra strength calcium antacid that contains 1000 mg of calcium carbonate and is designed to relieve acid indigestion and heartburn.

How should I take CAREOne™?

Adults and children 12 years of age and over should wet the tablet in their mouth before chewing and take 2-3 tablets as symptoms occur, or as directed by a doctor.

What is the maximum dosage for CAREOne™?

Do not take more than 7 tablets in a 24-hour period, and do not use the maximum dosage for more than 2 weeks unless advised by a doctor.

Are there any teratogenic effects associated with CAREOne™?

No teratogenic effects have been mentioned for CAREOne™.

Can I use CAREOne™ if I am pregnant or breastfeeding?

You should ask a health professional before using CAREOne™ if you are pregnant or breastfeeding.

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 CAREOne™ come in?

CAREOne™ is available in assorted berry flavors.

Is CAREOne™ gluten-free?

Yes, CAREOne™ is gluten-free.

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

Do not use CAREOne™ if the printed seal under the cap is torn or missing.

Can CAREOne™ interact with other medications?

Yes, antacids like CAREOne™ may interact with certain prescription drugs.

Packaging Info

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

Packaging configurations for Ultra Strength Antacid Assorted Berries.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

CAREOne™ is a calcium antacid formulated with 1000 mg of calcium carbonate per chewable tablet. Each bottle contains 72 chewable tablets, available in assorted berries flavors. This product is gluten-free and is designed for ultra strength relief, comparable to the active ingredient in Tums® Ultra Strength 1000 Assorted Berries. The National Drug Code (NDC) for this product is 72476-178-23.

Uses and Indications

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

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

Dosage and Administration

Adults and children 12 years of age and over should wet the tablets in their mouth before chewing. The recommended dosage is to chew 2 to 3 tablets as symptoms occur, or as directed by a healthcare professional. It is important to follow the prescribed instructions to ensure effective symptom management.

Contraindications

Use of this product is contraindicated in patients who exceed the recommended dosage of 7 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.

Warnings and Precautions

Healthcare professionals should be aware of the following critical information regarding the safe use of this product.

It is imperative that patients do not exceed a maximum dosage of 7 tablets within a 24-hour period. Additionally, the use of this product should not extend beyond 2 weeks unless specifically directed and supervised by a healthcare provider. This precaution is essential to prevent potential adverse effects associated with prolonged use or excessive dosing.

Currently, there are no specific warnings, general precautions, or laboratory tests associated with this product that have been provided. However, healthcare professionals should remain vigilant and monitor patients for any unusual symptoms or reactions during the course of treatment. In the event of any concerning side effects or if the patient feels unwell, it is advisable to reassess the treatment plan and consider alternative options.

Side Effects

Patients may experience various adverse reactions when using the medication. While no specific side effects are listed in this section, it is important to note that antacids may interact with certain prescription drugs, which could lead to unintended effects or diminished efficacy of the prescribed treatment.

In clinical practice, healthcare providers should be vigilant about potential interactions and monitor patients accordingly. It is advisable for patients to inform their healthcare providers of all medications they are taking 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. Patients should be counseled to separate the dosing of antacids and other drugs by at least two hours when possible to ensure optimal therapeutic outcomes.

Packaging & NDC

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

Packaging configurations for Ultra Strength Antacid Assorted Berries.
Details

Pediatric Use

Pediatric patients aged 12 years and older may use the medication at a dosage of 2-3 tablets chewed as symptoms occur, or as directed by a healthcare professional.

It is important to keep the medication out of reach of children to ensure safety.

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 weighed, 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 no specific data available 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 may necessitate dosage adjustments based on their level of renal function. It is essential for healthcare professionals to monitor renal function regularly in these patients. Dosage adjustments should be guided by creatinine clearance levels to ensure safe and effective therapy. Additionally, it is recommended to perform renal function tests prior to initiating therapy and periodically thereafter in patients with renal impairment.

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, healthcare professionals are advised to exercise caution when administering the medication. It is essential to monitor patients closely for any signs of adverse effects or symptoms that may arise from excessive dosing.

In the event of suspected overdosage, immediate medical attention should be sought. Healthcare providers should implement supportive measures as necessary, which may include symptomatic treatment and monitoring of vital signs.

Due to the lack of detailed overdosage information, it is recommended that healthcare professionals refer to established clinical guidelines and protocols for managing overdose situations relevant to the specific medication in question. Additionally, contacting a poison control center may provide further guidance on appropriate management strategies.

Continued vigilance and patient assessment are crucial in mitigating potential risks associated with overdosage.

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 available in the insert text.

Patient Counseling

Patients should be advised not to exceed a total of 7 tablets within a 24-hour period. Additionally, they should not use the maximum dosage of this product for more than 2 weeks unless directed by a healthcare professional.

It is important for patients to consult with their doctor or pharmacist prior to using this product if they are currently taking any prescription medications. This is particularly crucial as antacids may interact with certain prescription drugs, potentially affecting their efficacy or safety.

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 safety or efficacy.

Additional Clinical Information

The medication is administered orally. For adults and children aged 12 years and older, patients should wet the tablets in their mouth before chewing and can chew 2-3 tablets as symptoms occur or as directed by a healthcare professional. There is no additional information available regarding laboratory tests, abuse potential, patient counseling, or postmarketing experience.

Drug Information (PDF)

This file contains official product information for Ultra Strength Antacid Assorted Berries, 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 Antacid Assorted Berries, 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.