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Meijer Wild Berry Antacid Chews

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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)
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2024
Label revision date
December 18, 2025
Drug Information (PDF)
Prescribing information, PDF file
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
Pregnancy
See Pregnancy Use Section
Lactation
See Lactation Use Section
Marketed in the U.S.
Since 2024
Label revision date
December 18, 2025
Manufacturer
Meijer
Registration number
M001
NDC root
79481-0042
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

Meijer Wild Berry Antacid Chews are a type of chewable medication designed to provide relief from heartburn, sour stomach, acid indigestion, and upset stomach caused by these symptoms. They are formulated to help soothe discomfort and restore balance in your digestive system, making it easier for you to feel comfortable after eating.

These chews come in a pleasant wild berry flavor, making them a convenient and tasty option for managing occasional digestive issues. If you're experiencing any of the symptoms mentioned, these antacid chews may be a helpful addition to your routine.

Uses

If you're experiencing discomfort from heartburn, sour stomach, or acid indigestion, this medication can help relieve those symptoms. It’s also effective for soothing an upset stomach that arises from these issues.

You can feel confident using this medication, as there are no known teratogenic effects (which means it doesn't cause birth defects) associated with it. This makes it a safer option for those who may be concerned about such risks.

Dosage and Administration

You can take this medication by chewing and swallowing 1 to 2 chewable tablets every 2 to 4 hours as needed. This is suitable for adults and children aged 12 years and older. However, it's important not to exceed 5 chewable tablets in a 24-hour period to ensure your safety.

If you have a child under 12 years old, it's best to consult a doctor before giving them this medication. They can provide guidance on the appropriate dosage and whether it's suitable for your child's needs. Always follow these instructions carefully to use the medication safely and effectively.

What to Avoid

It's important to be mindful of how you use this medication. You should not take the maximum dosage for more than two weeks unless your doctor has specifically advised and is supervising you. This guideline helps ensure your safety and the effectiveness of the treatment.

While there are no specific contraindications or concerns about abuse, misuse, or dependence mentioned, always follow your healthcare provider's instructions closely to avoid any potential risks. If you have any questions or concerns about your medication, don't hesitate to reach out to your healthcare professional for guidance.

Side Effects

It's important to be aware of potential side effects when considering this medication. You should not use this product if you have ever experienced an allergic reaction to it or any of its ingredients. Allergic reactions can range from mild symptoms, like rashes, to severe reactions that may require immediate medical attention.

Always consult with your healthcare provider if you have any concerns about allergies or side effects related to this medication. Your safety is a priority, and understanding these warnings can help you make informed decisions about your health.

Warnings and Precautions

You should not use this product if you have ever had an allergic reaction to it or any of its ingredients. It's important to follow the recommended dosage; do not take the maximum dose for more than two 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 stop taking it and consult your doctor for guidance. Always prioritize your health and safety by seeking professional advice when needed.

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 giving this medication to children, it's important to follow specific guidelines. For adults and children aged 12 years and older, you can give 1 to 2 chewable tablets every 2 to 4 hours as needed, but make sure not to exceed 5 tablets in a 24-hour period.

If your child is under 12 years old, it's crucial to consult a doctor before administering this medication. This ensures their safety and that they receive the appropriate dosage for their age. Always prioritize your child's health by seeking professional advice when it comes to medications.

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 before starting the medication. 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 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 plan is safe and effective for your specific situation. They can help monitor your kidney health and make any necessary adjustments to your medications.

Hepatic Impairment

If you have liver problems, it's important to know that the information provided does not include specific guidelines for dosage adjustments, special monitoring, or precautions related to your condition. This means that there are no tailored recommendations for how the medication may affect you differently due to your liver health.

Always consult your healthcare provider for personalized advice and to ensure that any treatment plan is safe and effective for your specific situation. They can help you understand how to manage your health while taking any medications.

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 best performance of your product, store it in a dry place at a temperature between 20° to 25°C (68° to 77°F). This temperature range helps maintain the product's effectiveness and safety.

When handling the product, be sure to do so with clean hands and in a clean environment to avoid contamination. Always follow any specific instructions provided with the product for safe use and disposal.

Additional Information

No further information is available.

FAQ

What is Meijer Wild Berry Antacid Chews used for?

Meijer Wild Berry Antacid Chews relieve heartburn, sour stomach, acid indigestion, and upset stomach due to these symptoms.

Who can take Meijer Wild Berry Antacid Chews?

Adults and children 12 years and older can chew and swallow 1 to 2 tablets every 2-4 hours as needed. Children under 12 should consult a doctor.

What is the maximum dosage for Meijer Wild Berry Antacid Chews?

Do not exceed 5 chewable tablets in 24 hours.

Are there any warnings for using Meijer Wild Berry Antacid Chews?

Do not use if you have ever had an allergic reaction to this product or any of its ingredients.

Can I use Meijer Wild Berry Antacid Chews if I am pregnant or breastfeeding?

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

How should I store Meijer Wild Berry Antacid Chews?

Store the chews between 20° to 25°C (68° to 77°F) in a dry place.

Are there any contraindications for Meijer Wild Berry Antacid Chews?

No specific contraindications are mentioned in the provided text.

What should I do if I experience side effects?

The insert does not provide specific instructions for stopping use or calling a doctor regarding side effects.

Packaging Info

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

Packaging configurations for Meijer Wild Berry Antacid Chews.
Details

Drug Information (PDF)

This file contains official product information for Meijer Wild Berry Antacid Chews, 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 heartburn, sour stomach, acid indigestion, and upset stomach associated with these symptoms.

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

Dosage and Administration

Adults and children aged 12 years and older may chew and swallow 1 to 2 chewable tablets every 2 to 4 hours as needed for symptom relief. It is important not to exceed a total of 5 chewable tablets within a 24-hour period.

For children under 12 years of age, it is advised to consult a healthcare professional before administration.

Contraindications

There are no specified contraindications for this product. However, it is advised that the maximum dosage should not be used for more than 2 weeks unless under the guidance and supervision of a physician.

Warnings and Precautions

The use of this product is contraindicated in individuals with a known history of allergic reactions to the product or any of its components. Healthcare professionals should ensure that patients are screened for such allergies prior to administration.

It is imperative to adhere to dosage guidelines, particularly regarding the maximum dosage. Patients should not exceed the maximum dosage for a duration longer than 2 weeks unless specifically directed by a physician. This precaution is essential to mitigate the risk of potential adverse effects associated with prolonged high-dose use.

Currently, there are no specific recommendations for laboratory tests associated with the safe use of this product. Healthcare providers should remain vigilant and monitor patients for any signs of adverse reactions or complications during treatment.

In the event of any concerning symptoms or adverse reactions, patients should be advised to discontinue use and consult their healthcare provider for further evaluation and management.

Side Effects

Patients should be aware that the use of this product is contraindicated in individuals who have a history of allergic reactions to the product or any of its ingredients. This warning is critical to prevent serious allergic responses that may occur upon administration.

In clinical trials and postmarketing experiences, no additional adverse reactions have been reported beyond those associated with allergic reactions. Therefore, careful screening for prior allergic history is essential before initiating treatment with this product to ensure patient safety.

Drug Interactions

There are currently no documented drug interactions associated with 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 Meijer Wild Berry Antacid Chews (calcium carbonate). Columns show Packaging, Formulation Type, and Active Ingredient Strength.

Packaging configurations for Meijer Wild Berry Antacid Chews.
Details

Pediatric Use

Pediatric patients aged 12 years and older may chew and swallow 1 to 2 chewable tablets every 2 to 4 hours as needed, with a maximum of 5 chewable tablets in a 24-hour period. For children under 12 years of age, it is advised to consult a doctor before use.

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. It is advisable to monitor these patients closely for any adverse effects or changes in efficacy.

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 weighed, 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 safe use during pregnancy and lactation.

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 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 and prepared for potential scenarios involving overdose.

Healthcare providers should be aware that the clinical presentation of an overdose may vary significantly depending on the substance involved and the individual patient's characteristics. Symptoms of overdose can range from mild to severe and may include altered mental status, cardiovascular instability, respiratory distress, and gastrointestinal disturbances.

In the event of suspected overdosage, immediate medical evaluation is recommended. Healthcare professionals should assess the patient's vital signs and conduct a thorough clinical examination. Supportive care should be initiated as necessary, including airway management, oxygen supplementation, and intravenous fluids.

If the specific agent involved in the overdose is known, appropriate antidotes or specific treatments should be administered as indicated. Continuous monitoring of the patient is crucial to identify any evolving symptoms and to guide further management.

In all cases of suspected overdose, it is advisable to contact a poison control center or a medical toxicologist for expert guidance on management strategies tailored to the specific situation.

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 compound in these areas.

Postmarketing Experience

Postmarketing experience has included the collection of adverse event reports received voluntarily or through surveillance programs. Healthcare professionals and patients are encouraged to report any adverse events or side effects associated with the use of the product. For inquiries or to report an adverse event, individuals may contact 1-800-245-2898, available Monday through Friday from 9 AM to 4 PM EST.

Patient Counseling

Healthcare providers should advise patients to keep this product out of reach of children to prevent accidental ingestion.

Patients should be informed not to exceed the maximum dosage for more than two weeks unless directed by a physician. It is important for patients to understand the potential for constipation when using this product, and they should be encouraged to monitor their bowel habits.

Additionally, healthcare providers should recommend that patients consult with a doctor or pharmacist before using this product if they are currently taking any prescription medications. This is particularly crucial as antacids may interact with certain prescription drugs, and professional guidance can help avoid potential adverse effects.

Storage and Handling

The product is supplied in various package configurations, with specific NDC numbers available for identification. It is essential to store the product in a dry place, maintaining a temperature range of 20° to 25°C (68° to 77°F) to ensure optimal stability and efficacy. Proper handling and storage conditions are critical to preserving the integrity of the product.

Additional Clinical Information

No further data are available.

Drug Information (PDF)

This file contains official product information for Meijer Wild Berry Antacid Chews, 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 Meijer Wild Berry Antacid Chews, 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.