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Sunmark Regular Strength Antacid

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This product has been discontinued

Active ingredient
Calcium Carbonate 500 mg
Other brand names
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 2021
Label revision date
December 13, 2024
Drug Information (PDF)
Prescribing information, PDF file
Active ingredient
Calcium Carbonate 500 mg
Other brand names
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 2021
Label revision date
December 13, 2024
Manufacturer
Strategic Sourcing Services LLC
Registration number
M001
NDC root
70677-0137
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

Sunmark is an antacid tablet that contains 500 mg of calcium carbonate, which helps provide fast relief from heartburn and acid indigestion. If you experience discomfort from these conditions, Sunmark can help alleviate those symptoms effectively.

These chewable tablets come in an assorted fruit flavor and are designed for regular strength use, making them a convenient option for managing occasional digestive discomfort. Each package contains 150 tablets, ensuring you have plenty on hand when you need 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 (which means it doesn't cause birth defects) associated with this medication.

Dosage and Administration

If you are an adult or a child aged 12 years and older, you can take this medication by chewing 2 to 4 tablets whenever you experience symptoms, or as your doctor advises. Make sure to follow the guidance provided by your healthcare professional to ensure safe and effective use. Always remember to chew the tablets thoroughly before swallowing for the best results.

What to Avoid

It's important to use this medication responsibly to ensure your safety. You should not take more than 15 tablets within a 24-hour period, and avoid using the maximum dosage for more than 2 weeks unless your doctor has advised you to do so. Following these guidelines helps prevent potential health risks 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 should be aware that certain prescription medications can interact with antacids, which may affect how well your other medications work. It's important to discuss your current medications with your healthcare provider to avoid any potential issues.

Currently, there are no specific adverse reactions or warnings listed, but staying informed about how different medications can interact is crucial for your health. Always consult with your doctor if you have any concerns about your medications.

Warnings and Precautions

It's important to use this medication responsibly. You should not take more than 15 tablets in a 24-hour period, and you should avoid using 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 product, it's best to consult your doctor for guidance. Always prioritize your safety and well-being when taking any medication.

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 signs of overdose for this medication, general symptoms can include unusual drowsiness, confusion, or difficulty breathing. If you notice any of these signs, seek medical help right away.

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

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 adults and children aged 12 years and older. If your child is within this age range, they can chew 2 to 4 tablets as needed for symptoms, or follow your doctor's instructions.

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, don't hesitate to consult with your healthcare provider.

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. Specifically, if you have reduced creatinine clearance (a measure of how well your kidneys are filtering waste), your healthcare provider will closely monitor your condition. Regular renal function tests (tests that check how well your kidneys are working) should be performed to ensure your safety.

For those with significant renal impairment, a reduced dose of medication is recommended. Always communicate with your healthcare team about your kidney health to ensure you receive the appropriate care and adjustments needed for your treatment.

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 talk to your doctor or pharmacist before using this medication, especially if you are currently taking any prescription drugs. Some antacids can interact with these medications, which may affect how well they work or increase the risk of side effects.

Always keep your healthcare provider informed about all the medications you are taking, including over-the-counter products, to ensure your safety and the effectiveness of your treatment.

Storage and Handling

To ensure the safety and effectiveness of your product, store it in a cool place, keeping the temperature below 30ºC (86ºF). It's important to keep the container tightly closed to protect its contents. Before using, always check that the printed seal under the cap is intact; do not use the product if the seal is torn or open, as this could compromise its safety.

By following these simple storage and handling guidelines, you can help maintain the quality of the product and ensure your safety during use.

Additional Information

You can take this medication orally by chewing 2 to 4 tablets when symptoms occur, or as directed by your doctor. This guidance applies to both adults and children aged 12 years and older. If you have any questions about how to use this medication, be sure to consult your healthcare provider for personalized advice.

FAQ

What is sunmark?

Sunmark is an antacid tablet that provides fast relief of heartburn and acid indigestion.

What is the active ingredient in sunmark?

The active ingredient in sunmark is Calcium Carbonate, which is present at a dosage of 500 mg per tablet.

What symptoms does sunmark relieve?

Sunmark relieves acid indigestion and heartburn.

How should I take sunmark?

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

What is the maximum dosage for sunmark?

Do not take more than 15 tablets in a 24-hour period, and do not use the maximum dosage for more than 2 weeks without a doctor's advice.

Are there any contraindications for sunmark?

No specific contraindications are mentioned for sunmark.

Can I use sunmark if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before using sunmark.

What should I do if I am taking other prescription drugs?

Ask a doctor or pharmacist before use, as antacids may interact with certain prescription drugs.

How should I store sunmark?

Store sunmark below 30ºC (86ºF) and keep the container tightly closed. Do not use if the printed seal under the cap is torn or open.

What flavor does sunmark come in?

Sunmark comes in an assorted fruit flavor.

Packaging Info

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

Packaging configurations for Sunmark Regular Strength Antacid.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Sunmark is an antacid formulation available in the form of chewable tablets. Each tablet contains 500 mg of Calcium Carbonate as the active ingredient, providing regular strength for the fast relief of heartburn and acid indigestion. The product is offered in assorted fruit flavor and is packaged in a container containing 150 chewable tablets. The National Drug Code (NDC) for this product is 70677-0137-1.

Uses and Indications

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

There are no teratogenic effects associated with this drug, nor are there any nonteratogenic effects mentioned.

Dosage and Administration

Adults and children 12 years of age and over are instructed to chew 2 to 4 tablets as symptoms occur, or as directed by a healthcare professional. It is recommended that the tablets be chewed thoroughly before swallowing to ensure optimal absorption and efficacy.

Contraindications

Use of this product is contraindicated in patients who exceed the maximum dosage of 15 tablets within a 24-hour period or utilize the maximum dosage for more than 2 weeks without the advice and supervision of a healthcare professional.

Warnings and Precautions

Healthcare professionals should be aware of the following precautions associated with the use of this product.

General precautions must be observed to ensure patient safety. It is imperative that patients do not exceed a maximum intake of 15 tablets within a 24-hour period. Additionally, the maximum dosage should not be utilized for more than 2 weeks unless specifically advised and monitored by a healthcare provider. This limitation is crucial to prevent potential adverse effects associated with prolonged use or excessive dosage.

No specific laboratory tests have been identified for monitoring during the use of this product. However, healthcare professionals should remain vigilant and assess the patient's overall health and response to treatment regularly.

In the absence of specific emergency medical help instructions or directives to discontinue use, healthcare providers are encouraged to maintain open communication with patients regarding any unusual symptoms or concerns that may arise during treatment.

Side Effects

Patients should be aware of potential adverse reactions associated with the use of this medication. Currently, there are no specific adverse reactions listed in the available data. However, it is important to note that patients who are taking a prescription drug should exercise caution, as antacids may interact with certain prescription medications.

Healthcare providers should monitor patients for any unexpected effects, especially in those who are concurrently using other treatments. As with any medication, it is essential for patients to discuss their full medication regimen with their healthcare provider to mitigate the risk of adverse interactions.

Drug Interactions

Patients are advised to consult a healthcare professional, such as a doctor or pharmacist, prior to using this medication if they are currently taking any prescription drugs.

Antacids have the potential to interact with various prescription medications. The specific mechanisms of these interactions may vary, and the clinical effects can depend on the particular drugs involved. Therefore, it is essential for patients to seek professional guidance to ensure safe and effective use of antacids alongside their prescribed therapies. Monitoring and dosage adjustments may be necessary based on the specific interactions identified.

Packaging & NDC

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

Packaging configurations for Sunmark Regular Strength Antacid.
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. It is important to keep this medication out of reach of younger children to ensure safety.

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. 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 and those who are breastfeeding should consult a healthcare professional prior to using this medication. The potential risks and benefits must be carefully considered, 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 mothers.

Renal Impairment

Renal impairment may necessitate dosage adjustments for patients with reduced kidney function. It is essential that patients with reduced creatinine clearance are closely monitored to ensure safety and efficacy. Regular renal function tests should be performed in patients with kidney problems to assess their condition. For patients with significant renal impairment, a reduced dose is recommended to mitigate potential risks associated with decreased clearance.

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 and adhere to general principles of management in cases of suspected overdose.

It is essential to monitor the patient closely for any potential symptoms that may arise from an overdose. Symptoms can vary widely depending on the substance involved and the individual patient's response.

In the event of an overdose, immediate medical attention should be sought. Healthcare providers should implement supportive care measures, which may include maintaining airway patency, providing supplemental oxygen, and monitoring vital signs.

Additionally, it is recommended to consult local poison control centers or relevant toxicology resources for guidance on specific management protocols and antidotes, if applicable.

Documentation of the incident, including the substance involved, estimated dose, and time of exposure, is crucial for effective management and follow-up care.

Nonclinical Toxicology

There is currently no available information regarding teratogenic effects, non-teratogenic effects, or any relevant nonclinical toxicology data. Additionally, no details are provided concerning animal pharmacology and toxicology.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients not to exceed a maximum of 15 tablets within a 24-hour period. Additionally, patients should be informed that the maximum dosage of this product should not be used for more than 2 weeks unless directed by a healthcare professional.

It is also important for healthcare providers to encourage patients to consult with a doctor or pharmacist prior to using this product if they are currently taking any prescription medications. Patients should be made aware that antacids may interact with certain prescription drugs, and this interaction could affect the efficacy of their treatment.

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 a temperature not exceeding 30ºC (86ºF). Healthcare professionals are advised to inspect the product prior to use; it should not be utilized if the printed seal under the cap is torn or open.

Additional Clinical Information

The medication is administered orally. For adults and children aged 12 years and older, the recommended dosage is to chew 2-4 tablets as symptoms occur or as directed by a healthcare professional. 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 Sunmark Regular Strength Antacid, 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 Sunmark Regular Strength Antacid, 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.