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Antacid - Medication Information

Product NDC Code 17714-043
Drug Name

Antacid

Type Brand
Pharm Class Blood Coagulation Factor [EPC],
Calcium [CS],
Cations,
Divalent [CS],
Increased Coagulation Factor Activity [PE]
Active Ingredients
Calcium carbonate 500 mg/1
Route ORAL
Dosage Form TABLET, CHEWABLE
RxCUI drug identifier 308907
Application Number part331
Labeler Name Advance Pharmaceutical Inc.
Packages
Package NDC Code Description
17714-043-15 150 tablet, chewable in 1 bottle (17714-043-15)
17714-043-55 55 tablet, chewable in 1 bottle (17714-043-55)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient (in each tablet) Calcium Carbonate 500 mg

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions chew 1-2 tablets as symptoms occurs. do not take more than 8 tablets in 24 hours do not use the maximum dosage for more than 2 weeks

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Al-lakes (D&C red #27, D&C yellow # 10, FD&C blue #1, FD&C yellow # 6), dextrose, flavors (cherry, lemon, lime, orange), magnesium stearate, maltodextrin

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
Uses relieves acid indigestion heartburn sour stomach

Purpose

Information about the drug product’s indications for use.
Purpose Antacid

Spl product data elements

Usually a list of ingredients in a drug product.
ANTACID Calcium Carbonate DEXTROSE MAGNESIUM STEARATE MALTODEXTRIN CHERRY CALCIUM CARBONATE CALCIUM CATION AP;043 Cherry,Lemon,Orange

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL Calcium Carbonate 500 mg Antacid tablets NDC: 17714-043-15 – 150 COUNT b43c92b6-figure-01 b43c92b6-figure-02 1

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other Information each tablet contains: calcium 200 mg store at room temperature 15-30 °C (59-86 °F)

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions or Comments Call 631-981-4600, Monday-Friday, 8.30 am – 4.30 pm ET TAMPER EVIDENT: DO NOT USE IF IMPRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING Manufactured by: Advance Pharmaceutical Inc. Holtsville, NY 11742

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings Ask a doctor before use if you have kidney stones a calcium-restricted diet ask a doctor or pharmacist before use if you are taking a prescription drug. Antacids may interact with certain prescription drugs. Stop use and ask a doctor if symptoms last more than 2 weeks.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API