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Equaline Ultra Strength Antacid Assorted Berry

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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 2024
Label revision date
May 12, 2024
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 2024
Label revision date
May 12, 2024
Manufacturer
UNITED NATURAL FOODS, INC. DBA UNFI
Registration number
part331
NDC root
41163-184
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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Drug Overview

Equqline® Ultra Strength is an antacid that contains 1000 mg of calcium carbonate, which helps relieve symptoms of acid indigestion and heartburn. This medication works by neutralizing stomach acid, providing you with quick relief from discomfort associated with these conditions.

Available in a tasty assorted berry flavor, Equqline® Ultra Strength comes in two convenient sizes: 160 chewable tablets and 72 chewable tablets, making it easy to find the right option for your needs.

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 (which means it doesn't cause birth defects) associated with this medication.

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, you should chew 2 to 3 tablets as your symptoms arise, or follow your doctor's instructions if they have provided specific guidance.

Make sure to take the tablets only when necessary, and remember that it's important to follow the recommended dosage to ensure safe and effective use. If you have any questions or concerns about how to take the medication, don’t hesitate to reach out to your healthcare provider for advice.

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 no specific side effects are listed, these interactions could affect how well your other medications work. Always consult with your healthcare provider if you have concerns about combining antacids with your prescriptions.

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 while using this product, it's best to consult your doctor for guidance. Always prioritize your health and well-being by following these precautions.

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, or if you are concerned about a possible overdose, seek medical help right away.

In case of an overdose, contacting your local emergency services or going to the nearest hospital is crucial. Always keep the medication packaging with you, as it can help healthcare professionals understand what you've taken. Remember, it's better to be safe and get checked out if you have any doubts.

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 with a doctor before use, as specific guidelines for their age group may differ. Always prioritize safety and follow the advice of 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 considering this medication, it’s important to consult with a healthcare provider. 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 based on how well your kidneys are functioning. Regular monitoring of your kidney function tests is essential to ensure your safety and the effectiveness of your treatment.

For those with a creatinine clearance (a measure of kidney function) of less than 30 mL/min, a reduced dose of medication is recommended. Additionally, if you have severe renal impairment, special care should be taken, as this can lead to higher levels of the drug in your system and increase the risk of side effects. Always consult your healthcare provider for personalized advice and adjustments to your treatment plan.

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 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 your other medications could affect how well those medications work.

To ensure your treatment is safe and effective, always discuss any medications, 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 safety and effectiveness of your product, store it in a cool, dry place at temperatures below 30˚C (86˚F). This helps maintain its quality and performance. Before using the product, always check that the printed seal under the cap is intact; do not use it if the seal is torn or missing, as this could indicate that the product is compromised.

By following these simple storage and handling guidelines, you can help ensure that the product remains safe and effective for your use.

Additional Information

You should take this medication orally. For adults and children aged 12 and older, place the tablets in your mouth to wet them before chewing. Chew 2-3 tablets as needed for symptoms, or follow your doctor's instructions.

FAQ

What is Equqline® Ultra Strength?

Equqline® Ultra Strength is an antacid tablet that contains 1000 mg of Calcium Carbonate, designed to relieve acid indigestion and heartburn.

How should I take Equqline® Ultra Strength?

For adults and children 12 years of age and over, wet the tablet in your mouth before chewing and chew 2-3 tablets as symptoms occur, or as directed by a doctor.

Are there any contraindications for Equqline® Ultra Strength?

No specific contraindications are mentioned for Equqline® Ultra Strength.

What should I do if I am pregnant or breastfeeding?

If you are pregnant or breastfeeding, ask a health professional before using Equqline® Ultra Strength.

What are the storage instructions for Equqline® Ultra Strength?

Store Equqline® Ultra Strength below 30˚C (86˚F) and do not use if the printed seal under the cap is torn or missing.

What is the maximum dosage for Equqline® Ultra Strength?

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

Can Equqline® Ultra Strength interact with other medications?

Yes, antacids like Equqline® Ultra Strength may interact with certain prescription drugs.

What flavors are available for Equqline® Ultra Strength?

Equqline® Ultra Strength is available in an assorted berry flavor.

What sizes does Equqline® Ultra Strength come in?

Equqline® Ultra Strength is available in two sizes: 160 Chewable Tablets and 72 Chewable Tablets.

Packaging Info

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

Packaging configurations for Equaline Ultra Strength Antacid Assorted Berry.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

Equqline® Ultra Strength antacid tablets contain Calcium Carbonate as the active ingredient, providing 1000 mg per tablet. These chewable tablets are formulated to relieve heartburn and acid indigestion. The product is available in assorted berry flavor and is offered in two packaging sizes: 160 chewable tablets (NDC 63868-184-75) and 72 chewable tablets (NDC 63868-184-68).

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

For adults and children aged 12 years and over, the recommended administration involves wetting the mouth prior to chewing. Patients should chew 2 to 3 tablets as symptoms occur, or as directed by a healthcare professional. It is important to follow the prescribed dosage to ensure optimal efficacy and safety.

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. Adherence to these dosage recommendations is essential to prevent potential adverse effects.

Warnings and Precautions

Healthcare professionals should be aware of the following precautions associated with the 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 maximum dosage should not be utilized for more than 2 weeks unless specifically advised and monitored by a healthcare provider. This precaution is essential to mitigate the risk of potential adverse effects associated with prolonged use or excessive dosing.

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 as part of standard care practices.

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

Side Effects

Patients may experience various adverse reactions when using the medication. Notably, there are no specific side effects listed in the warnings section. However, it is important to note that antacids may interact with certain prescription drugs, which could lead to unintended effects or reduced efficacy of the medications involved.

Healthcare providers should be aware of these potential interactions and monitor patients accordingly to ensure safe and effective use of the medication in conjunction with antacids.

Drug Interactions

Antacids have the potential to interact with various prescription medications, which may affect the absorption and efficacy of these drugs. It is advisable for healthcare professionals to monitor patients closely when antacids are co-administered with other medications.

In cases where antacids are prescribed alongside other drugs, dosage adjustments may be necessary to mitigate the risk of reduced therapeutic effects. Patients should be counseled on the timing of antacid administration relative to their other medications to optimize therapeutic outcomes.

Packaging & NDC

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

Packaging configurations for Equaline Ultra Strength Antacid Assorted Berry.
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

There is no specific information available 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. Monitoring for potential adverse effects and therapeutic efficacy is recommended in 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 evaluated in these populations to ensure maternal and fetal safety.

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 require dosage adjustments based on their level of kidney function. It is essential to monitor renal function tests regularly in these patients to ensure safe and effective treatment. For patients with a creatinine clearance of less than 30 mL/min, a reduced dose is recommended to mitigate the risk of adverse effects. Special consideration should be given to patients with severe renal impairment, as they may experience increased drug accumulation and toxicity, necessitating careful management and monitoring.

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 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 use of the compound in these contexts.

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 use if they are currently taking any prescription medications. This is crucial as antacids may interact with certain prescription drugs, potentially leading to adverse effects or reduced efficacy of the medications.

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, 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.

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 Equaline Ultra Strength Antacid Assorted Berry, 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 Equaline Ultra Strength Antacid Assorted Berry, 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.