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Mckesson antacid calcium carbonate - Medication Information

Product NDC Code 68599-1411
Drug Name

Mckesson antacid calcium carbonate

Type Brand
Pharm Class Blood Coagulation Factor [EPC],
Calcium [CS],
Cations,
Divalent [CS],
Increased Coagulation Factor Activity [PE]
Active Ingredients
Calcium carbonate 420 mg/1
Route ORAL
Dosage Form TABLET, CHEWABLE
RxCUI drug identifier 313884
Application Number part331
Labeler Name McKesson Medical-Surgical
Packages
Package NDC Code Description
68599-1411-3 250 packet in 1 box (68599-1411-3) / 2 tablet, chewable in 1 packet
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Calcium Carbonate 420 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 Adults and children: (12 years and older) Chew 2 tablets every 2 - 3 hours or as symptoms occu, repeat hourly if needed. Do not exceed 19 tablets in 24 hours. Children under 12 years: Ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients aspartame, croscarmellose sodium, magnesium stearate, maltodextrin, mineral oil, mint flavor, sorbitol

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 sour stomach heartburn upset stomach associated with these symptoms

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.
McKesson Antacid Calcium Carbonate Calcium carbonate ASPARTAME SORBITOL MINERAL OIL MAGNESIUM STEARATE CALCIUM CARBONATE CALCIUM CATION CARBONATE ION CROSCARMELLOSE SODIUM MALTODEXTRIN AZ;036

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.
McKesson Antacid Tablets Calcium Carbonate 420 mg NDC 68599-1411-3 Tablets for acid indigestion, gas, and heartburn. 2 Per Pack 250 Packs Per Box MFR #87675 101R Antacid Label 4-13-21

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.
Drug Facts

Ask doctor or pharmacist

Information about when a doctor or pharmacist should be consulted about drug/drug or drug/food interactions before using a drug product.
Ask a doctor or pharmacist before use if you are presently taking a prescription drug. Antacids may interact with certain prescription drugs. have kidney disease

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use the maximum dosage of this product for more than 2 weeks except under the advice and supervision of a doctor

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.

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information calcium content per tablet: 168 mg Phenylketonurics : each tablet may contain 1.5 mg phenylalanine store at room temperature 59-86°F (15-30°C) in a dry place tamper-evident sealed packets do not use any opened or torn packets

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 1-800-777-4908

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product do not take more than 19 tablets in a 24 hour period. If symptoms persist for more than 2 weeks, stop using this product and see a doctor.

Pregnancy or breast feeding

Pregnancy or Breast feeding
If pregnant or breast feeding, ask a health professional before use.

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

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