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Loratadine - Medication Information

Product NDC Code 30142-996
Drug Name

Loratadine

Type Generic
Active Ingredients
Loratadine 5 mg/1
Route ORAL
Dosage Form TABLET, CHEWABLE
RxCUI drug identifier 665078
Application Number ANDA210088
Labeler Name KROGER COMPANY
Packages
Package NDC Code Description
30142-996-30 3 blister pack in 1 carton (30142-996-30) / 10 tablet, chewable in 1 blister pack
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient (in each tablet) Loratadine USP, 5 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 6 years and over chew 2 tablets daily; not more than 2 tablets in 24 hours children 2 to under 6 years of age chew 1 tablet daily; not more than 1 tablet in 24 hours children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor
adults and children 6 years and over chew 2 tablets daily; not more than 2 tablets in 24 hours
children 2 to under 6 years of age chew 1 tablet daily; not more than 1 tablet in 24 hours
children under 2 years of age ask a doctor
consumers with liver or kidney disease ask a doctor

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients aspartame, citric acid anhydrous, colloidal silicon dioxide, D&C red No. 27 aluminum lake, FD&C blue No. 2 aluminum lake, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid

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 temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose • sneezing • itchy, watery eyes • itching of the nose or throat

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Loratadine Loratadine LORATADINE LORATADINE ASPARTAME ANHYDROUS CITRIC ACID SILICON DIOXIDE D&C RED NO. 27 FD&C BLUE NO. 2 MAGNESIUM STEARATE MANNITOL MICROCRYSTALLINE CELLULOSE STEARIC ACID SODIUM STARCH GLYCOLATE TYPE A POTATO light purple to dark purple 753

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.
Principal Display Panel – 30 Chewable Tablet Blister Pack Carton NDC 30142-996-30 † Compare to the active ingredient of Children’s Claritin® Chewables ages 2 years and older Non-Drowsy Children’s Allergy Relief Loratadine Chewable Tablets USP, 5 mg Antihistamine Indoor & Outdoor Allergies 30 CHEWABLE TABLETS The chewable tablets are to be chewed before swallowing. Grape Flavored 24 Hour Relief Of: • Sneezing • Runny Nose • Itchy, Watery Eyes • Itchy Nose or Throat * When taken as directed. See Drug Facts Panel. 30 count carton

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.
Distributed by: Ohm Laboratories Inc. New Brunswick, NJ 08901 0418

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 (1-800-222-1222).

Other safety information

Information about safe use and handling of the product that may not have been specified in another field.
Other information • Phenylketonurics: contains phenylalanine 1.25 mg per tablet. • TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING. • store between 20° to 25°C (68° and 77°F).

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? call 1-800-406-7984 Keep the carton. It contains important information. See end panel for expiration date.

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 Do not use if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctorbefore use if you have liver or kidney disease. Your doctor should determine if you need a different dose. When using this product do not take more than directed. Taking more than directed may cause drowsiness. Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away. If pregnant or breast-feeding, ask a health professional before. Keep Out of Reach of Children In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).

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