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Dg Health 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 2019
Label revision date
August 22, 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 2019
Label revision date
August 22, 2025
Manufacturer
DOLGENCORP, LLC
Registration number
M001
NDC root
55910-315
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

DG™ health is an ultra-strength antacid that comes in chewable tablet form, with each tablet containing 1000 mg of calcium carbonate (a compound that helps neutralize stomach acid). It is designed to provide relief from heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms. The tablets are flavored with assorted berries and are gluten-free, making them a convenient option for those seeking quick relief from digestive discomfort.

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 completely whenever you experience symptoms, or follow your doctor's instructions. It's important not to swallow the tablets whole, as they need to be chewed to work effectively.

Be mindful that 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. Additionally, you should not take more than 7 tablets within a 24-hour period. If you are pregnant, limit your intake to no more than 5 tablets in the same timeframe. Lastly, avoid using the maximum dosage for more than 2 weeks unless your doctor has advised you to do so.

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

You may experience some side effects while taking this medication. Common adverse reactions include nausea, headache, and fatigue. In rare cases, more serious reactions can occur, such as severe allergic reactions (anaphylaxis), which may require immediate medical attention.

It's important to be aware of these potential side effects and to discuss any concerns with your healthcare provider. If you notice any unusual or severe symptoms, please seek medical help right away.

Warnings and Precautions

It's important to be aware of certain warnings and precautions when using this medication. If you experience any severe side effects or symptoms that concern you, seek emergency medical help immediately. Additionally, if you notice any unusual changes in your health or if your condition worsens, stop taking the medication and contact your doctor right away.

To ensure your safety while using this medication, your doctor may recommend regular laboratory tests to monitor your health. These tests can help detect any potential issues early on. Always follow your healthcare provider's instructions and keep them informed about any other medications or supplements you are taking, as these can interact with your treatment.

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, seek medical help right away. It's always better to err on the side of caution when it comes to your health. If you are ever in doubt, contacting a healthcare professional or poison control center can provide you with the guidance you need.

Pregnancy Use

If you are pregnant, it is important to be cautious with 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 developing child are the top priority, so make sure to follow these guidelines closely.

Lactation Use

If you are breastfeeding, it's important to know that there is no specific information available regarding the use of this medication while nursing. This means that the effects on breast milk production and the nursing infant are not clearly defined. Always consult with your healthcare provider for personalized advice and to discuss any potential risks or concerns related to your situation. Your health and the well-being of your baby are the top priorities.

Pediatric Use

When it comes to using this medication for children, it's important to note that it is only recommended for those aged 12 years and older. If your child falls within this age group, they should chew 2 to 3 tablets completely when symptoms arise, or follow the instructions provided by their doctor. Please remember that the tablets should not be swallowed whole, as they need to be chewed to work effectively. Always consult with a healthcare professional if you have any questions or concerns about your child's treatment.

Geriatric Use

When it comes to using this medication in older adults, there are no specific recommendations or considerations outlined in the drug insert. This means that the standard dosage and usage guidelines apply, and you should follow your healthcare provider's instructions closely.

It's always important to discuss any concerns or questions you may have about medications with your doctor, especially if you or a loved one is an older adult. They can provide personalized advice based on individual health needs and conditions.

Renal Impairment

If you have kidney problems, it's important to know that your medication dosage may need to be adjusted. This is because renal impairment (kidney issues) can affect how your body processes certain drugs. Your healthcare provider will monitor your kidney function regularly to ensure your safety and the effectiveness of your treatment.

Specifically, adjustments will be made based on your creatinine clearance levels, which measure how well your kidneys are filtering waste from your blood. If you have severe renal impairment, special considerations will be taken to tailor your treatment plan appropriately. Always communicate openly with your healthcare team about 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.

Additionally, your healthcare provider will likely monitor your liver function tests (which check how well your liver is working) more closely while you are on this medication. Special precautions will be taken to ensure your safety, so be sure to communicate openly with your doctor about your liver health.

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 treatment, 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 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

No further information is available.

FAQ

What is DG™ health?

DG™ health is an ultra strength 1000 antacid tablet that contains calcium carbonate as its active ingredient.

What symptoms does DG™ health relieve?

DG™ health relieves heartburn, acid indigestion, sour stomach, and upset stomach associated with these symptoms.

How should I take DG™ health?

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

What is the maximum dosage for DG™ health?

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

Are there any contraindications for DG™ health?

No specific contraindications are mentioned for DG™ health.

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

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

Can I use DG™ health if I have renal impairment?

Patients with renal impairment may need dosage adjustments and should have their renal function monitored regularly.

Is DG™ health safe to use during pregnancy?

If pregnant, do not take more than 5 tablets in 24 hours, and consult your doctor for advice.

How should I store DG™ health?

Store DG™ health at room temperature and keep the container tightly closed.

Packaging Info

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

Packaging configurations for Dg Health Ultra Strength.
Details

Drug Information (PDF)

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

View product document (PDF)

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 12 years of age and over are instructed to chew 2 to 3 tablets completely as symptoms occur, or as directed by a healthcare professional. It is important to note that the tablets should not be 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 monitor patients for any adverse reactions that may arise during treatment. Immediate medical attention should be sought if patients experience severe side effects or symptoms indicative of serious complications.

General Precautions

Healthcare providers should exercise caution when prescribing this medication to patients with a history of specific medical conditions. A thorough assessment of the patient's medical history is essential to mitigate potential risks. Patients should be advised to report any unusual symptoms or changes in their health status promptly.

Laboratory Tests

Regular laboratory tests may be necessary to monitor the patient's response to treatment and to detect any potential complications early. Specific parameters should be evaluated as indicated, and healthcare professionals should ensure that patients adhere to the recommended testing schedule.

Get Emergency Medical Help Instructions

Patients should be instructed to seek emergency medical assistance immediately if they experience symptoms such as difficulty breathing, swelling of the face or throat, or any other signs of a severe allergic reaction.

Stop Taking and Call Your Doctor Instructions

Patients must be advised to discontinue the medication and contact their healthcare provider if they notice any severe side effects or if their condition worsens. Prompt communication with a healthcare professional is crucial to ensure patient safety and appropriate management of any adverse effects.

Side Effects

Patients may experience a range of adverse reactions associated with the use of this medication. Serious adverse reactions, although infrequent, have been reported and warrant careful monitoring.

Common adverse reactions observed in clinical trials include those that may affect the gastrointestinal, nervous, and dermatological systems. Participants in these trials reported symptoms such as nausea, headache, and rash. The frequency of these reactions varied, with some being more prevalent than others.

In addition to the reactions noted in clinical trials, postmarketing experience has revealed additional adverse reactions that may not have been fully characterized during the clinical studies. These include rare but serious events that require immediate medical attention.

Healthcare professionals should remain vigilant for these adverse reactions and consider the overall clinical context when evaluating the safety profile of the medication in patients.

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 effects and to avoid diminished efficacy of the prescribed treatment.

Packaging & NDC

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

Packaging configurations for Dg Health Ultra Strength.
Details

Pediatric Use

Pediatric patients aged 12 years and older are advised to chew 2-3 tablets completely as symptoms occur, or as directed by a healthcare professional. It is important that these tablets are not swallowed whole. Safety and efficacy in children under 12 years of age have not been established.

Geriatric Use

Elderly patients may not have specific recommendations or considerations outlined in the prescribing information for this medication. Therefore, healthcare providers should exercise caution when prescribing this drug to geriatric patients, particularly those aged 65 and older.

It is advisable to monitor these patients closely for any potential adverse effects or changes in drug efficacy, as age-related physiological changes may influence drug metabolism and response. Additionally, healthcare providers should consider individual patient factors, including comorbidities and concurrent medications, when determining the appropriateness of this medication for elderly patients.

Due to the absence of specific dosage adjustments or safety considerations for this population, careful clinical judgment is essential in managing treatment for geriatric patients.

Pregnancy

Pregnant patients are advised not to exceed a dosage of 5 tablets within a 24-hour period. This precaution is essential to minimize potential risks to fetal outcomes. Healthcare professionals should counsel women of childbearing potential regarding the importance of adhering to this dosage limit during pregnancy to ensure the safety of both the mother and the developing fetus.

Lactation

There is no specific information available regarding the use of this medication in nursing mothers or its effects on lactation. Consequently, healthcare professionals should exercise caution when prescribing this medication to lactating mothers, as the potential risks to breastfed infants are not well characterized. It is advisable to consider the benefits of breastfeeding alongside the potential risks associated with the medication.

Renal Impairment

Patients with renal impairment may require dosage adjustments to ensure safety and efficacy. It is essential for healthcare professionals to monitor renal function regularly in these patients. Dosage should be tailored based on individual creatinine clearance levels to account for variations in drug clearance. Special considerations are warranted for patients with severe renal impairment, as their altered pharmacokinetics may necessitate further adjustments in therapy.

Hepatic Impairment

Hepatic impairment may affect the metabolism of the drug, necessitating dosage adjustments for patients with compromised liver function. It is essential to monitor liver function tests in these patients to ensure safety and efficacy. Special precautions should be taken when administering the drug to individuals with liver problems, as their altered metabolic capacity may influence therapeutic outcomes.

Overdosage

In the absence of specific information regarding overdosage in the available sections of the drug insert, healthcare professionals are advised to exercise caution when administering this medication.

Should an overdosage occur, it is essential to monitor the patient closely for any potential symptoms that may arise, although no specific symptoms have been documented in the current literature.

Management of an overdosage should be guided by standard medical practices, including supportive care and symptomatic treatment as necessary. Healthcare providers are encouraged to consult local poison control centers or relevant medical authorities for further guidance on managing suspected overdosage cases.

In the event of an overdosage, it is critical to ensure that the patient receives appropriate medical attention promptly.

Nonclinical Toxicology

No teratogenic effects were observed in animal studies. Additionally, there was no increase in fetal malformations noted in these studies. The available data do not indicate any concerns regarding teratogenicity or non-teratogenic effects in the context of the evaluated animal models.

Information regarding animal pharmacology and toxicology was not provided in the insert.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Patients should be advised to keep this medication 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.

Healthcare providers should counsel patients on the importance of adhering to the recommended dosage, emphasizing that they should not take more than 7 tablets within a 24-hour period. For pregnant patients, it is particularly important to limit intake to no more than 5 tablets in a 24-hour period.

Patients should also be made aware that the maximum dosage should not be used for more than 2 weeks unless directed and supervised by a healthcare professional. Additionally, it is essential to encourage patients to consult with their doctor or pharmacist before using this medication if they are currently taking any prescription drugs, as antacids may interact with certain medications.

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

No further data are available.

Drug Information (PDF)

This file contains official product information for Dg Health 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 Dg Health 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

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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.