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Qch Ultra Strength Antacid 171af

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This product has been discontinued

Active ingredient
Calcium Carbonate 1000 mg
Other brand names
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
Marketed in the U.S.
Since 2024
Label revision date
August 3, 2024
Active ingredient
Calcium Carbonate 1000 mg
Other brand names
Dosage form
Tablet, Chewable
Route
Oral
Prescription status
OTC (over the counter)
CSA schedule
Not a scheduled drug
Marketed in the U.S.
Since 2024
Label revision date
August 3, 2024
Manufacturer
Chain Drug Marketing Association Inc.
Registration number
M001
NDC root
83324-127

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Drug Overview

Quality Choice Ultra Strength Antacid Tablets are chewable tablets that contain calcium carbonate (a substance that helps neutralize stomach acid) as their active ingredient. Each tablet provides 1000 mg of calcium carbonate and comes in an assorted fruit flavor, making them easy to take.

These antacid tablets are primarily used to relieve symptoms of acid indigestion and heartburn, providing quick relief when you need it. They are comparable to the active ingredient found in Ultra Strength Tums®, making them a reliable option for managing discomfort related to excess stomach acid.

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 occur after eating.

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

To use this medication effectively, start by wetting your mouth before chewing the tablets. For adults and children aged 12 and older, you should chew 2 to 3 tablets whenever you experience symptoms, or follow your doctor's instructions if they have provided specific guidance.

Make sure to take the tablets as needed, ensuring that you chew them well for the best results. Always consult with your healthcare provider if you have any questions about how to use this medication or if your symptoms persist.

What to Avoid

It's important to use this medication responsibly to ensure your safety. You should not take more than 7 tablets within a 24-hour period. Additionally, 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 may experience some interactions if you take antacids alongside certain prescription medications. It's important to be aware that while there are no specific side effects listed for this medication, interactions can still occur. Always consult with your healthcare provider about any medications you are taking to ensure they work safely together.

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.

Before using this product, make sure to consult with your doctor or pharmacist if you are currently taking any prescription medications, as antacids can interact with some of them. If you experience any unusual symptoms or have concerns, stop taking the medication and reach out to your healthcare provider for guidance.

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 or have concerns about an overdose, 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 professional assistance if you think something is wrong.

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

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 dosage is to chew 2-3 tablets when symptoms occur, or as directed by a healthcare professional.

If you have younger children, please consult your doctor for appropriate guidance, as this medication is not intended for them. Always prioritize safety and follow the instructions provided by your healthcare provider.

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 always wise to discuss any medications with a healthcare provider, especially since older individuals may have different health needs and responses to treatments.

Since there are no dosage adjustments or special precautions mentioned for elderly patients, your healthcare provider can help determine the best approach based on individual health conditions and any other medications being taken. Always prioritize open communication with your doctor to ensure safe and effective use of any medication.

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. Regular renal function tests (tests that check how well your kidneys are working) are essential to ensure your safety and the effectiveness of your treatment.

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 best care possible.

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 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 in a cool, dry place at temperatures below 30°C (86°F). This helps maintain its effectiveness and safety.

When handling the product, be sure to check that the printed seal under the cap is intact. If the seal is torn or missing, do not use the product, as this may indicate that it has been compromised. Following these guidelines will help you use the product safely and effectively.

Additional Information

You can take this medication orally. If you are an adult or a child aged 12 years and older, you should chew 2 to 3 tablets when symptoms occur, or follow your doctor's instructions. There are no additional details available regarding laboratory tests, abuse potential, or patient counseling information.

FAQ

What is Quality Choice Ultra Strength Antacid Tablets used for?

Quality Choice Ultra Strength Antacid Tablets are used to relieve acid indigestion and heartburn.

What is the active ingredient in this antacid?

The active ingredient is Calcium Carbonate, with a dosage of 1000mg per tablet.

How should I take Quality Choice Ultra Strength Antacid Tablets?

Adults and children 12 years of age and over should chew 2-3 tablets as symptoms occur, or as directed by a doctor.

Are there any dosage restrictions?

Do not take more than 7 tablets in a 24-hour period, or use the maximum dosage for more than 2 weeks without a doctor's advice.

Can I use this antacid if I am pregnant or breastfeeding?

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

Are there any known side effects?

No specific side effects are listed for Quality Choice Ultra Strength Antacid Tablets.

Can this antacid interact with other medications?

Yes, antacids may interact with certain prescription drugs, so consult a doctor or pharmacist if you are taking other medications.

How should I store this medication?

Store below 30°C (86°F) and do not use if the printed seal under the cap is torn or missing.

Is there any special consideration for patients with kidney problems?

Yes, patients with renal impairment may need dosage adjustments and should be closely monitored.

What flavor do the tablets come in?

The tablets come in an assorted fruit flavor.

Packaging Info

Below are the non-prescription pack sizes of Qch Ultra Strength Antacid 171af (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Qch Ultra Strength Antacid 171af.
Details

Drug Information (PDF)

This file contains official product information for Qch Ultra Strength Antacid 171af, including active ingredients, dosage, warnings, and labeling as submitted by the manufacturer for OTC distribution.

View product document (PDF)

Description

This product is identified by NDC 83324-127-72 and is marketed under the brand name Quality Choice. It is formulated as Ultra Strength Antacid Tablets, each containing 1000 mg of Calcium Carbonate as the active ingredient. The tablets are available in an assorted fruit flavor and are presented in a package containing 72 chewable tablets. This formulation is comparable to the active ingredient found in Ultra Strength Tums®.

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 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.

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 warnings and precautions associated with the use of this product.

General precautions must be observed to ensure safe usage. It is imperative that patients do not exceed a maximum of 7 tablets within a 24-hour period. Additionally, the maximum dosage should not be utilized for more than 2 weeks unless directed and supervised by a healthcare provider.

Before recommending this product, healthcare professionals should advise patients to consult with a doctor or pharmacist if they are currently taking any prescription medications. This is particularly important as antacids may interact with certain prescription drugs, potentially leading to adverse effects or diminished therapeutic efficacy.

No specific warnings or laboratory tests have been identified for this product; however, vigilance in monitoring patient responses and interactions is essential for safe administration.

Side Effects

Patients should be aware that no specific side effects have been listed for this medication. However, it is important to note that antacids may interact with certain prescription drugs, which could lead to altered efficacy or increased risk of adverse reactions associated with those medications.

Healthcare providers should monitor patients for any potential interactions and advise them accordingly. As with any treatment, patients are encouraged to report any unexpected symptoms or concerns to their healthcare provider.

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 can alter the gastric pH, which may impact the solubility and subsequent absorption of certain drugs. Therefore, healthcare professionals should consider advising patients to space the administration of antacids and other medications appropriately, typically by allowing a gap of at least two hours between doses.

Packaging & NDC

Below are the non-prescription pack sizes of Qch Ultra Strength Antacid 171af (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Qch Ultra Strength Antacid 171af.
Details

Pediatric Use

Pediatric patients should be advised to keep this medication out of reach of children. For children aged 12 years and older, the recommended dosage is to chew 2-3 tablets as symptoms occur, or as directed by a healthcare professional.

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 potential 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 in these populations to ensure the safety of both the mother and the fetus or infant.

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

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 the risk of adverse effects.

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 context of overdosage, it is important to note that the available sections of the drug insert do not provide specific information regarding potential overdosage scenarios.

Healthcare professionals are advised to exercise caution and consider the possibility of overdosage when administering the medication. In the absence of detailed guidance, it is recommended that clinicians monitor patients closely for any unusual symptoms or adverse reactions that may arise following administration.

In the event of suspected overdosage, standard supportive measures should be implemented. This includes ensuring the patient's safety, providing symptomatic treatment, and considering the need for further medical evaluation. Healthcare providers should remain vigilant and prepared to manage any complications that may occur as a result of overdosage, even in the absence of specific symptoms outlined in the drug insert.

For further management, consultation with a poison control center or a medical toxicologist may be beneficial to guide treatment decisions and ensure optimal patient care.

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 use of the compound in question.

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 7 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 configuration that includes an NDC number for identification. It is essential to store the product at temperatures below 30°C (86°F) to maintain its integrity and efficacy.

Healthcare professionals should ensure that the product is not used if the printed seal under the cap is torn or missing, as this may indicate potential tampering or contamination. Proper handling and storage conditions are crucial for ensuring the safety and effectiveness of the product.

Additional Clinical Information

The medication is administered orally. For adults and children aged 12 years and older, the recommended dosage is to 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 Qch Ultra Strength Antacid 171af, 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 Qch Ultra Strength Antacid 171af, 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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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.