Loratadine LORATADINE BRYANT RANCH PREPACK FDA Approved USE(S) temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose itchy, watery eyes sneezing itching of the nose or throat

LORATADINE

Generic: LORATADINE
Mfr: BRYANT RANCH PREPACK FDA OTC
FunFoxMeds bottle
Substance Loratadine
Route
ORAL
Applications
ANDA211718
Product NDC
71335-2391-00 71335-2391-01 71335-2391-02 71335-2391-03 71335-2391-04 71335-2391-05 71335-2391-06 71335-2391-07 71335-2391-08 71335-2391-09
Package NDC
71335-2391-1 71335-2391-2 71335-2391-3 71335-2391-4 71335-2391-5 71335-2391-6 71335-2391-7 71335-2391-8 71335-2391-9

Drug Facts

Composition & Profile

Active Ingredients
ACTIVE INGREDIENT(S) Active ingredient (in each tablet) Loratadine USP 10 mg
Inactive Ingredients
INACTIVE INGREDIENTS corn starch lactose monohydrate magnesium stearate pregelatinized starch
Strengths
10 mg
Quantities
20 tablets 30 tablets 60 tablets 14 tablets 10 tablets 90 tablets 28 tablets 15 tablets 100 tablets
Treats Conditions
Use S Temporarily Relieves These Symptoms Due To Hay Fever Or Other Upper Respiratory Allergies Runny Nose Itchy Watery Eyes Sneezing Itching Of The Nose Or Throat
Pill Appearance
Shape: round Color: white Imprint: H;L20

Identifiers & Packaging

Container Type BOTTLE
NDC 71335-2391-00
All Product Codes
71335-2391-00 71335-2391-01 71335-2391-02 71335-2391-03 71335-2391-04 71335-2391-05 71335-2391-06 71335-2391-07 71335-2391-08 71335-2391-09
UNII
7AJO3BO7QN
SPL Set IDs
baad51cd-daa0-4920-a6d5-2faaaaea7956
Packaging

HOW SUPPLIED Loratadine 10mg Tablet NDC 71335-2391-1: 20 Tablets in a BOTTLE NDC 71335-2391-2: 30 Tablets in a BOTTLE NDC 71335-2391-3: 60 Tablets in a BOTTLE NDC 71335-2391-4: 14 Tablets in a BOTTLE NDC 71335-2391-5: 10 Tablets in a BOTTLE NDC 71335-2391-6: 90 Tablets in a BOTTLE NDC 71335-2391-7: 28 Tablets in a BOTTLE NDC 71335-2391-8: 15 Tablets in a BOTTLE NDC 71335-2391-9: 100 Tablets in a BOTTLE Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504; Loratadine 10mg Tablet Label

Package Descriptions
  • HOW SUPPLIED Loratadine 10mg Tablet NDC 71335-2391-1: 20 Tablets in a BOTTLE NDC 71335-2391-2: 30 Tablets in a BOTTLE NDC 71335-2391-3: 60 Tablets in a BOTTLE NDC 71335-2391-4: 14 Tablets in a BOTTLE NDC 71335-2391-5: 10 Tablets in a BOTTLE NDC 71335-2391-6: 90 Tablets in a BOTTLE NDC 71335-2391-7: 28 Tablets in a BOTTLE NDC 71335-2391-8: 15 Tablets in a BOTTLE NDC 71335-2391-9: 100 Tablets in a BOTTLE Repackaged/Relabeled by: Bryant Ranch Prepack, Inc. Burbank, CA 91504
  • Loratadine 10mg Tablet Label
Overview

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

Indications & Usage

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

Dosage & Administration

DIRECTIONS adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor

Warnings & Precautions
WARNINGS
Purpose

PURPOSE Antihistamine

Do Not Use

DO NOT USE if you have ever had an allergic reaction to this product or any of its ingredients.

When Using

WHEN USING THIS PRODUCT do not take more than directed. Taking more than directed may cause drowsiness.

Stop Use & Ask a Doctor

STOP USE AND ASK DOCTOR IF an allergic reaction to this product occurs. Seek medical help right away.

Keep Out of Reach of Children

KEEP OUT OF REACH OF CHILDREN In case of overdose, get medical help or contact a Poison Control Center right away.

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Additional Information

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