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D-Cal

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Active ingredient
Calcium Carbonate 750 mg
Other brand names
Drug classes
Blood Coagulation Factor, Phosphate Binder
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2025
Label revision date
December 1, 2025
Active ingredient
Calcium Carbonate 750 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
Marketed in the U.S.
Since 2025
Label revision date
December 1, 2025
Manufacturer
A&Z Pharmaceutical Inc.
Registration number
Part331
NDC root
62211-247

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Drug Overview

D-cal-62 chewable tablets are designed to help relieve discomfort from heartburn, acid indigestion, sour stomach, and upset stomach caused by these symptoms. If you're experiencing any of these issues, D-cal-62 can provide you with the relief you need to feel more comfortable.

Uses

If you're experiencing discomfort from heartburn, acid indigestion, or a sour stomach, this medication can help relieve those symptoms. It’s also effective for soothing an upset stomach that arises from these issues. You can feel more comfortable and get back to your daily activities without the nagging discomfort.

Rest assured, this medication does not have any known teratogenic effects, meaning it does not cause developmental issues in a fetus.

Dosage and Administration

When using this medication, it's important to follow the recommended dosage to ensure your safety and effectiveness. For adults, you should not take more than 10 tablets within a 24-hour period. If you are giving this medication to a child, the maximum is 5 tablets in the same timeframe.

Always keep track of how many tablets you have taken to avoid exceeding these limits. If you have any questions or concerns about the dosage, be sure to consult with a healthcare professional for guidance.

What to Avoid

You can feel confident using this medication, as there are no specific contraindications, controlled substance classifications, or concerns regarding abuse, misuse, or dependence associated with it. This means that, based on the available information, there are no known reasons that would prevent you from taking this medication safely. Always remember to follow your healthcare provider's guidance and reach out if you have any questions or concerns about your treatment.

Side Effects

It's important to be aware that if you are taking any prescription medications, you should consult with your doctor or pharmacist before using this product. Antacids can interact with certain prescription drugs, which may affect how well they work or increase the risk of side effects.

Always prioritize your health by discussing any potential interactions with your healthcare provider to ensure safe and effective use.

Warnings and Precautions

Before using this medication, it's important to consult with your doctor or pharmacist, especially if you are currently taking any prescription drugs. Antacids can interact with certain medications, which may affect how well they work.

While there are no specific general precautions or laboratory tests mentioned, always stay alert to how your body responds to any new medication. If you experience any unusual symptoms or have concerns, don’t hesitate to reach out to your healthcare provider for guidance.

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 unusual drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it’s crucial to seek immediate medical help.

In case of an emergency, contact your local emergency services or go to the nearest hospital. Always keep medications out of reach of children and follow the prescribed dosage to prevent any potential risks. If you have any concerns or questions about your medication, don’t hesitate to reach out to your healthcare provider for guidance.

Pregnancy Use

When considering the use of D-CAL (calcium carbonate) tablets during pregnancy, it's important to note that there is no specific information available regarding its safety, dosage adjustments, or any special precautions for pregnant individuals. This means that the effects of this medication on pregnancy have not been clearly established.

If you are pregnant or planning to become pregnant, it is always best to consult with your healthcare provider before taking any medication, including D-CAL. They can provide personalized advice based on your health needs and ensure the safety of both you and your baby.

Lactation Use

If you are breastfeeding or planning to breastfeed, it's important to know that there is no specific information available about the use of D-CAL (calcium carbonate) tablets in nursing mothers. This means that the effects on breast milk and nursing infants have not been studied or documented.

As always, it's best to consult with your healthcare provider before taking any medication while breastfeeding to ensure the safety and well-being of both you and your baby.

Pediatric Use

When giving this medication to children, you should have them chew one tablet daily. If their symptoms continue, it's important to consult a doctor for further advice. Be cautious not to exceed a total of five tablets in a 24-hour period, as this is the maximum safe amount for children.

Always remember to keep the medication out of reach of children to prevent accidental ingestion. Your vigilance is key to ensuring their safety while using this product.

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 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.

It's always best to discuss your individual situation with your healthcare provider, who can offer personalized advice and ensure that any medications you take are safe and effective for you.

Hepatic Impairment

If you have liver problems, it's important to know that the drug insert does not provide specific information about dosage adjustments, special monitoring, or precautions for your condition. This means that there are no tailored guidelines for how this medication may affect you if you have hepatic impairment (liver issues).

Always consult your healthcare provider for personalized advice and to discuss any concerns regarding your liver health and how it may relate to your treatment. They can help ensure that you receive the safest and most effective 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 safety and effectiveness of your product, store it in a dry place. This helps maintain its quality and prevents any damage. Before using the product, always check that the imprinted seal under the cap is intact; do not use it if the seal is torn or open, as this could indicate that the product has been compromised. Following these simple guidelines will help you use the product safely and effectively.

Additional Information

No further information is available.

FAQ

What is D-cal-62-chewable-tablets used for?

D-cal-62-chewable-tablets relieve heartburn, acid indigestion, sour stomach, and upset stomach due to these symptoms.

What is the recommended dosage for adults?

Adults should chew 2 tablets daily, but do not take more than 10 tablets in a 24-hour period.

What is the recommended dosage for children?

Children should chew 1 tablet daily, with a maximum of 5 tablets in a 24-hour period. If symptoms persist, consult a doctor.

Are there any contraindications for using D-cal-62-chewable-tablets?

No contraindications are listed for D-cal-62-chewable-tablets.

Should I consult a doctor before using this medication?

Yes, ask a doctor or pharmacist before use if you are taking a prescription drug, as antacids may interact with certain medications.

Is there any information about using D-cal-62-chewable-tablets during pregnancy?

No specific information regarding the use of D-cal-62-chewable-tablets during pregnancy is provided.

How should D-cal-62-chewable-tablets be stored?

Store D-cal-62-chewable-tablets in a dry place and do not use if the imprinted seal under the cap is torn or open.

Are there any warnings associated with D-cal-62-chewable-tablets?

You should consult a doctor or pharmacist if you are taking prescription drugs, as there may be interactions.

Packaging Info

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

Packaging configurations for D-Cal.
Details

Drug Information (PDF)

This file contains official product information for D-Cal, 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, sour stomach, and upset stomach associated with these symptoms.

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

Dosage and Administration

The recommended dosage for adults is a maximum of 10 tablets within a 24-hour period. For pediatric patients, the maximum dosage is limited to 5 tablets in a 24-hour period.

Healthcare professionals should ensure that patients are advised not to exceed these specified limits to avoid potential adverse effects. It is essential to monitor the patient's response to the medication and adjust the dosage as necessary, while remaining within the established maximum limits.

Contraindications

There are no contraindications associated with the use of this product. It is deemed safe for use in the absence of specific conditions or situations that would warrant avoidance.

Warnings and Precautions

Healthcare professionals are advised to exercise caution when recommending the use of this product, particularly in patients who are currently taking prescription medications. It is essential to consult with a doctor or pharmacist prior to use, as antacids may interact with certain prescription drugs, potentially leading to adverse effects or diminished therapeutic efficacy.

No specific general precautions or laboratory tests have been identified for this product. Therefore, ongoing assessment of the patient's overall health and medication regimen is recommended to ensure safe and effective use.

Side Effects

Patients should be advised to consult a healthcare professional, such as a doctor or pharmacist, prior to using this product if they are currently taking any prescription medications. This precaution is necessary as antacids may interact with certain prescription drugs, potentially leading to adverse reactions or diminished efficacy of the prescribed treatment. It is essential for patients to disclose their complete medication regimen to ensure safe and effective use of the product.

Drug Interactions

There are currently no documented drug interactions associated with this medication. Additionally, there are no known 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 D-Cal (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for D-Cal.
Details

Pediatric Use

Pediatric patients are advised to chew 1 tablet daily. If symptoms persist, it is recommended that a healthcare professional be consulted. The maximum dosage for children should not exceed 5 tablets within a 24-hour period. Additionally, it is important to keep this 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

There is no specific information regarding the use of D-CAL (calcium carbonate) tablets, chewable, in pregnant patients. The prescribing information does not provide safety concerns, dosage modifications, or special precautions related to the use of this medication during pregnancy. Healthcare professionals should consider the lack of data when prescribing D-CAL to women of childbearing potential and weigh the potential benefits against any unknown risks to fetal outcomes. It is advisable to monitor pregnant patients closely if D-CAL is deemed necessary.

Lactation

There is no specific information available regarding the use of D-CAL (calcium carbonate) tablets, chewable, in nursing mothers or its effects on lactation. Consequently, the safety and efficacy of this medication in lactating mothers and its potential impact on breastfed infants remain undetermined. Healthcare professionals should exercise caution and consider the lack of data when advising lactating mothers on the use of this product.

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 these patients to ensure safety and efficacy.

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 outlined 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 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 indicate an overdose. These may include, but are not limited to, increased severity of known side effects, unusual behavioral changes, or any other atypical clinical manifestations.

Management of an overdose should be guided by the clinical presentation of the patient. Supportive care is paramount, and symptomatic treatment should be initiated as necessary. It is recommended that healthcare professionals consult local poison control centers or relevant toxicology resources for specific guidance on the management of overdose cases.

In summary, while specific overdosage information is not available, healthcare professionals should exercise caution, remain observant for potential overdose symptoms, and implement appropriate management strategies as needed.

Nonclinical Toxicology

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

Postmarketing Experience

No postmarketing experience details are available in the insert.

Patient Counseling

Healthcare providers should advise patients to keep this medication out of reach of children to prevent accidental ingestion or misuse. It is important to emphasize the necessity of proper storage and handling to ensure the safety of young individuals.

Storage and Handling

The product is supplied in a secure packaging format, ensuring integrity and safety. It is essential to store the product in a dry place to maintain its efficacy and quality. Healthcare professionals should be vigilant and refrain from using the product if the imprinted seal under the cap is torn or open, as this may indicate potential contamination or compromise of the product. Proper handling and storage conditions are crucial for ensuring the product remains safe for use.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for D-Cal, 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 D-Cal, 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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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.