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Fevia Acid Control

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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 2026
Label revision date
March 19, 2026
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 2026
Label revision date
March 19, 2026
Manufacturer
VIVUNT PHARMA LLC
Registration number
M001
NDC root
82706-027
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

FEVIA™ is an antacid that contains 1000 mg of calcium carbonate, designed to help relieve symptoms such as acid indigestion, sour stomach, heartburn, and upset stomach. It comes in a chewable tablet form with a pleasant assorted berries flavor, making it easy to take without the need for water.

This medication works by neutralizing stomach acid, providing quick relief from discomfort associated with these common digestive issues. With 160 chewable tablets in each package, FEVIA™ offers a convenient option for managing occasional stomach upset.

Uses

If you're experiencing discomfort from acid indigestion, sour stomach, heartburn, or an upset stomach related to these issues, this medication can help relieve those symptoms. It’s designed to provide you with quick relief, 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, making it a safer option for those 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 instructs. It's important to pay attention to how long your symptoms last. If they continue for more than 2 weeks, you should consult your doctor before taking any more of the medication, as this could indicate a more serious health issue. Always follow your healthcare provider's advice for the best results.

What to Avoid

It's important to use this product safely to avoid potential risks. You should not use the maximum dosage for more than 2 weeks unless your doctor advises you to do so. Additionally, make sure not to exceed 6 tablets within a 24-hour period. Following these guidelines will help ensure your safety while using this medication.

Side Effects

When using this product, it's important to be aware of potential side effects and interactions. You should consult a doctor if you are currently taking any prescription medications, as antacids may interact with them. It's also crucial not to exceed 6 tablets in a 24-hour period and to avoid using the maximum dosage for more than 2 weeks unless directed by a physician. If you are pregnant or breastfeeding, please seek advice from a healthcare professional before using this product. Always keep it out of reach of children to ensure their safety.

Warnings and Precautions

Before using this product, it's important to consult your doctor if you are currently taking any prescription medications, as antacids can interact with certain drugs. Be mindful not to exceed 6 tablets in a 24-hour period, and avoid using the maximum dosage for more than 2 weeks unless directed by a physician. If you are pregnant or breastfeeding, please seek advice from a healthcare professional before use. Always keep this product out of reach of children.

While there are no specific laboratory tests required for this product, it's essential to follow these guidelines to ensure your safety and well-being. If you experience any concerning symptoms, do not hesitate to reach out to your healthcare provider for further guidance.

Overdose

It appears that there is no specific information available regarding overdosage for this medication. However, it's important to be aware of the general signs of an overdose, which can include symptoms like extreme drowsiness, confusion, or difficulty breathing. If you suspect an overdose, it is crucial to seek immediate medical help.

In case of an emergency, call your local emergency number 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

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 aged 12 years and older, you should have them chew 2 to 3 tablets as symptoms arise, or follow your doctor's instructions. It's important to keep this medication out of reach of younger children to ensure their safety. Always consult with a healthcare professional if you have any questions or concerns about its use in your child.

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 keep in mind that older adults may have different responses to medications, so discussing any concerns with a doctor is essential for ensuring safety and effectiveness.

Renal Impairment

If you have kidney problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or safety considerations related to renal impairment (kidney issues). This means that there are no tailored recommendations for how your treatment may need to change based on your kidney function.

Always consult your healthcare provider for personalized advice and to ensure that your treatment is safe and effective, especially if you have any concerns about your kidney health.

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 differently due to your liver health.

Always consult your healthcare provider for personalized advice and to discuss any concerns you may have regarding your liver condition and the use of this medication. They can help ensure that you receive the safest and most effective treatment.

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 feel free to ask questions and share your complete list of medications and any lab tests you may be undergoing. This way, you can receive the best possible care tailored to your needs.

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). It's important to keep it away from light, heat, and moisture, as these elements can affect its effectiveness.

When handling the product, make sure to do so in a clean environment to maintain its integrity. Always follow any specific disposal instructions provided to ensure safety and compliance.

Additional Information

No further information is available.

FAQ

What is FEVIA™?

FEVIA™ is an antacid that contains 1000 mg of Calcium Carbonate and is available in assorted berries flavor as chewable tablets.

What symptoms does FEVIA™ relieve?

FEVIA™ relieves acid indigestion, sour stomach, heartburn, and upset stomach associated with these symptoms.

How should I take FEVIA™?

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 FEVIA™?

Do not take more than 6 tablets in a 24-hour period and do not use the maximum dosage for more than 2 weeks unless advised by a doctor.

Are there any contraindications for using FEVIA™?

No specific contraindications are mentioned for FEVIA™.

Can I use FEVIA™ if I am pregnant or breastfeeding?

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

What should I do if I am taking other medications?

Ask a doctor before using FEVIA™ if you are currently taking a prescription drug, as antacids may interact with certain medications.

How should I store FEVIA™?

Store FEVIA™ below 30°C (86°F) and protect it from light, heat, and moisture.

What should I do if symptoms persist?

Do not take FEVIA™ for symptoms that persist for more than 2 weeks unless advised by a doctor, as this could indicate a serious condition.

Is there a risk of dependence or abuse with FEVIA™?

There are no specified risks of dependence or abuse associated with FEVIA™.

Packaging Info

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

Packaging configurations for Fevia Acid Control.
Details

Drug Information (PDF)

This file contains official product information for Fevia Acid Control, 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 specified drug.

Uses and Indications

This drug is indicated for the relief of symptoms associated with acid indigestion, sour stomach, heartburn, and upset stomach.

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

Dosage and Administration

Adults and children aged 12 years and older are instructed to chew 2 to 3 tablets as symptoms occur, or as directed by a healthcare professional. It is important to note that if symptoms persist for more than 2 weeks, the individual should seek medical advice, as this may indicate a serious underlying condition.

Contraindications

The use of this product is contraindicated in the following situations:

  • Maximum dosage should not be used for more than 2 weeks unless advised and supervised by a physician, due to potential risks associated with prolonged use.

  • Administration of more than 6 tablets within a 24-hour period is contraindicated to prevent adverse effects related to excessive dosage.

Warnings and Precautions

Healthcare professionals should exercise caution when recommending this product. It is imperative to advise patients to consult a physician prior to use if they are currently taking any prescription medications, as antacids may interact with certain drugs.

When administering this product, it is crucial to adhere to the recommended dosage guidelines. Patients should not exceed 6 tablets within a 24-hour period. Furthermore, the maximum dosage should not be utilized for more than 2 weeks unless directed and monitored by a healthcare provider.

For patients who are pregnant or breastfeeding, it is essential to seek guidance from a health professional before use to ensure safety for both the mother and child. Additionally, this product should be stored out of reach of children to prevent accidental ingestion.

Currently, there are no specific laboratory tests recommended for monitoring the use of this product. However, healthcare providers should remain vigilant and provide appropriate counsel to patients regarding the safe use of this medication.

Side Effects

Patients may experience various adverse reactions associated with the use of this product. It is important to note that individuals currently taking prescription medications should consult a healthcare professional prior to use, as antacids may interact with certain prescription drugs.

When using this product, patients should adhere to the recommended dosage guidelines, which specify not to exceed 6 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 physician.

For pregnant or breastfeeding individuals, it is advised to seek guidance from a health professional before using this product. Furthermore, to ensure safety, the product should be kept out of reach of children.

Drug Interactions

There are currently no documented drug interactions associated with the use of this medication. Additionally, there is no information available regarding 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 Fevia Acid Control (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Fevia Acid Control.
Details

Pediatric Use

Pediatric patients aged 12 years and older may chew 2-3 tablets as symptoms occur, or as directed by a healthcare professional. 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

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 currently no available data regarding the excretion of this medication 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 have not been specifically addressed in the available prescribing information. There are no dosage adjustments, special monitoring requirements, or safety considerations outlined for individuals with reduced kidney function. Healthcare professionals should exercise caution and consider the lack of data when prescribing to this patient population.

Hepatic Impairment

Patients with hepatic impairment have not been specifically studied in relation to this drug. Consequently, there are no 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 prescribing 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.

Healthcare providers should be aware that symptoms of overdosage may vary depending on the individual and the circumstances surrounding the event. In cases where an overdose is suspected, it is recommended to monitor the patient closely for any adverse effects or unusual symptoms that may arise.

Management of an overdose should include immediate supportive care. This may involve the following steps:

  1. Assessment: Conduct a thorough evaluation of the patient's clinical status, including vital signs and level of consciousness.

  2. Supportive Care: Provide symptomatic treatment as necessary, which may include intravenous fluids, oxygen supplementation, or other interventions based on the patient's needs.

  3. Consultation: Engage with a poison control center or toxicology specialist for guidance on specific management strategies tailored to the situation.

It is crucial for healthcare professionals to document the incident thoroughly and report any adverse events to the appropriate regulatory authorities as per local guidelines.

Nonclinical Toxicology

If pregnant or breastfeeding, it is advised to consult a health professional prior to use. No specific non-teratogenic effects have been identified. Additionally, there are no detailed findings related to nonclinical toxicology or animal pharmacology and toxicology available.

Postmarketing Experience

No postmarketing experience details are available in the insert text.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion. It is important to inform patients that they should not use the maximum dosage of this product for more than 2 weeks unless directed and supervised by a physician.

Patients should be cautioned against exceeding a maximum of 6 tablets within a 24-hour period to avoid potential adverse effects. Additionally, healthcare providers should encourage patients to consult with their doctor before using this product if they are currently taking any prescription medications, as antacids may interact with certain drugs.

Storage and Handling

The product is supplied in packaging that ensures its integrity during storage and handling. It must be stored at temperatures below 30°C (86°F) to maintain its efficacy. Additionally, it is essential to protect the product from light, heat, and moisture to prevent degradation. Proper storage conditions are critical to ensure the product remains safe and effective for use.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Fevia Acid Control, 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 Fevia Acid Control, 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.