EQUALINE extra strength antacid

ANTACID ORAL HUMAN OTC DRUG

EQUALINE extra strength antacid is an FDA drug label for the active ingredient ANTACID manufactured by SUPERVALU INC administered by ORAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20171227.

Generic name
ANTACID
Manufacturer
SUPERVALU INC
Product type
HUMAN OTC DRUG
Route
ORAL
Dosage form
N/A
NDC
41163-102
Application
part331
Label effective
20171227

About this product

EQUALINE extra strength antacid is an FDA-registered drug product whose active ingredient is ANTACID. It is labelled by SUPERVALU INC taken by oral and marketed as a human otc drug product. Identifiers on file: NDC 41163-102, application part331, label effective 20171227. It is one of 2 FDA drug label records sharing the active ingredient ANTACID. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ANTACID are most often described in connection with: relieves heartburn, acid indigestion, sour stomach. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredient (per tablet) Calcium Carbonate USP 750mg

Indications & Usage

Uses relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms

Dosage & Administration

Directions • adults and children 12 years of age and over: chew 2-4 tablets as symptoms occur ,or as directed by a doctor • do not take for symptoms that persist for more than 2 weeks unless advised by a doctor

Warnings

Warnings Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. When using this product • do not take more than 10 tablets in 24 hours • if pregnant do not take more than 6 tablets in 24 hours • do not use the maximum dosage for more than 2 weeks except under the advice and supervision of a doctor

More products with the same ingredient

ANTACID

EQUALINE regular strength antacid

SUPERVALU INC View label

How products containing ANTACID compare

FDA lists 2 drug label records with ANTACID as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

Dosage formProductsManufacturerProducts
— — SUPERVALU INC 2
— — — —
— — — —
— — — —
— — — —

Frequently asked questions

What is EQUALINE extra strength antacid used for?
Uses relieves • heartburn • acid indigestion • sour stomach • upset stomach associated with these symptoms

Who makes EQUALINE extra strength antacid?
SUPERVALU INC is the labeler of record for EQUALINE extra strength antacid. 2 FDA label records share the active ingredient ANTACID, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does EQUALINE extra strength antacid come in?
administered by oral. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is EQUALINE extra strength antacid prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing ANTACID?
Yes. 2 FDA drug label records list ANTACID as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has EQUALINE extra strength antacid been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.