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Equ Ultra Strength Antacid Assorted Fruit 171af

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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
41163-171
Drug Information (PDF)
Prescribing information, PDF file
Packaging Info (2 NDCs)
Packaging & NDC Codes (2)

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Drug Overview

EQUALINE® is an ultra strength antacid tablet that contains 1000 mg of calcium carbonate, a compound that helps neutralize stomach acid. You can use EQUALINE® to relieve symptoms of acid indigestion and heartburn, providing quick comfort when you need it.

These chewable tablets come in assorted fruit flavors and are available in two sizes: 160 tablets and 72 tablets. EQUALINE® is comparable to Tums® Ultra Strength 1000, making it a reliable option for managing your digestive discomfort.

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. It's important to note that there are no reported teratogenic effects (which means it doesn't cause birth defects) associated with this medication, making it a safer option for those who may be concerned about such risks.

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 3 tablets whenever you experience symptoms, or as your doctor advises. Make sure to follow your doctor's instructions for the best results. Chewing the tablets allows the medication to work quickly to help relieve your symptoms.

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 risks associated with misuse and ensures that you are using the medication effectively. Always consult with your healthcare provider if you have any questions or concerns about your treatment.

Side Effects

It's important to be aware of potential interactions if you are currently taking prescription medications, as antacids may affect how these drugs work. This could lead to reduced effectiveness or increased side effects of your prescription medication.

If you experience any unusual symptoms or reactions while using antacids, it's a good idea to consult your healthcare provider for guidance. Always keep them informed about all the medications you are taking to ensure your safety and well-being.

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 about your health while using this medication, stop taking it and call your doctor for guidance. Always prioritize your health and safety by following these instructions closely.

Overdose

If you suspect an overdose, it's important to stay calm and take immediate action. While there are no specific signs or symptoms listed for an overdose, you should be aware of general warning signs such as extreme drowsiness, confusion, or difficulty breathing. If you notice any of these symptoms or feel something is wrong, seek medical help right away.

In case of an overdose, contacting your healthcare provider or local poison control center is crucial. They can provide guidance on what steps to take next. Always err on the side of caution—if you are unsure, it’s best to get help immediately.

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 those aged 12 years and older. If your child is within this age range, they can chew 2-3 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 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. This is because your renal function, which is how well your kidneys are working, can affect how your body processes certain medications. Your healthcare provider will monitor your kidney function regularly, especially through tests that measure creatinine clearance (a test that estimates how well your kidneys filter waste).

Before starting any new treatment, your renal function should be tested, and these tests will continue periodically to ensure your safety. If you have moderate to severe renal impairment, you may require a reduced dose of your medication to avoid potential complications. Always discuss your kidney health with your doctor to ensure the best care.

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 for the medication do not change based on liver function. However, it’s always a good idea to discuss your liver health with your healthcare provider before starting any new medication. They can help ensure that your treatment is safe and effective for you.

Make sure to keep your doctor informed about any liver issues you may have, as they may want to monitor your health closely while you are on 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 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 best quality and safety of your product, store it at room temperature and keep the container tightly closed. This helps maintain its effectiveness and prevents contamination.

Before using, always check that the printed seal under the cap is intact. If the seal is torn or missing, do not use the product, as this could indicate that it has been compromised. Following these simple steps will help you use the product safely and effectively.

Additional Information

You should take this medication orally. Before using it, consult with your doctor or pharmacist, especially if you are currently taking any prescription drugs, as antacids can interact with some medications. If you are pregnant or breastfeeding, it's important to seek advice from a healthcare professional before use.

FAQ

What is EQUALINE®?

EQUALINE® is an ultra strength antacid tablet that contains 1000 mg of calcium carbonate.

What does EQUALINE® relieve?

EQUALINE® relieves acid indigestion and heartburn.

How should I take EQUALINE®?

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

What is the maximum dosage for EQUALINE®?

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.

Are there any contraindications for EQUALINE®?

No specific contraindications are mentioned for EQUALINE®.

Can EQUALINE® interact with other medications?

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

Is EQUALINE® safe to use during pregnancy or breastfeeding?

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

How should EQUALINE® be stored?

Store EQUALINE® at room temperature, keep the container tightly closed, and do not use if the printed seal under the cap is torn or missing.

What should I do if I have renal impairment?

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

Packaging Info

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

Packaging configurations for Equ Ultra Strength Antacid Assorted Fruit 171af.
Details

Drug Information (PDF)

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

View product document (PDF)

Description

EQUALINE® ultra strength antacid tablets contain Calcium Carbonate as the active ingredient, providing 1000 mg per tablet. These tablets are formulated to relieve heartburn and acid indigestion. The product is available in assorted fruit flavors and is offered in two packaging sizes: 160 chewable tablets (NDC 41163-171-75) and 72 chewable tablets (NDC 41163-171-68).

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

Adults and children 12 years of age and over are instructed to chew 2 to 3 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 effectiveness.

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 critical information regarding the safe 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 use of this product should not extend beyond 2 weeks unless directed and supervised by a healthcare provider. This precaution is essential to prevent potential adverse effects associated with prolonged use or excessive dosage.

Currently, there are no specific warnings, general precautions, or laboratory tests associated with this product that have been identified. However, healthcare professionals should remain vigilant and monitor patients for any unusual symptoms or reactions during the course of treatment.

In the event of any concerning symptoms or if the patient experiences adverse effects, it is crucial to advise them to discontinue use and consult their healthcare provider promptly.

Side Effects

Patients should be aware of potential adverse reactions associated with the use of this medication. While specific serious adverse reactions are not detailed, it is important to note that interactions may occur with other medications.

In particular, patients currently taking prescription drugs should exercise caution, as antacids may interact with certain prescription medications. This interaction could potentially alter the effectiveness of the prescribed treatment or lead to unexpected side effects.

Healthcare providers are encouraged to monitor patients for any unusual symptoms or changes in their condition, especially when initiating therapy with this medication alongside other treatments.

Drug Interactions

Antacids may interact with various prescription medications, potentially affecting their absorption and efficacy. It is advisable to separate the administration of antacids and other medications by at least two hours to minimize the risk of interaction. Monitoring for therapeutic effectiveness of the affected medications is recommended when antacids are used concurrently.

Packaging & NDC

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

Packaging configurations for Equ Ultra Strength Antacid Assorted Fruit 171af.
Details

Pediatric Use

Pediatric patients aged 12 years and older may use the medication as directed for symptom relief. The recommended dosage for this age group is to chew 2-3 tablets as symptoms occur or as directed by a healthcare professional.

It is important to keep the 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. 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 before 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 the safety of both the mother and the developing fetus.

Lactation

Lactating mothers are advised to consult a health professional prior to using this medication. There is currently no available data 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 renal function. It is essential to monitor renal function regularly in these patients to ensure safe and effective therapy. Dosage adjustments should be guided by creatinine clearance levels, with reduced doses being necessary for those with moderate to severe renal impairment. Prior to initiating therapy, renal function tests should be conducted, and ongoing assessments should be performed periodically to monitor any changes in renal status.

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 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 amount and timing of the substance taken, is crucial for effective treatment and follow-up care.

Nonclinical Toxicology

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

Postmarketing Experience

No postmarketing experience details are available for SPL code 90375-7.

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. 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 room temperature to ensure optimal conditions. Healthcare professionals are advised not to use the product if the printed seal under the cap is torn or missing, as this may indicate compromised safety or efficacy.

Additional Clinical Information

The medication is administered orally. Clinicians should advise patients to consult a doctor or pharmacist prior to use if they are currently taking any prescription medications, as antacids may interact with certain drugs. Additionally, patients who are pregnant or breastfeeding should seek guidance from a healthcare professional before using this medication.

Drug Information (PDF)

This file contains official product information for Equ Ultra Strength Antacid Assorted Fruit 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 Equ Ultra Strength Antacid Assorted Fruit 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.

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.