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Childrens Allegra Allergy by Chattem, Inc.

Medically reviewed on August 22, 2017

Dosage form: tablet, orally disintegrating
Ingredients: FEXOFENADINE HYDROCHLORIDE 30mg
Labeler: Chattem, Inc.
NDC Code: 41167-4232

Childrens Allegra Allergy

Drug Facts

Active ingredient

(in each tablet)

Fexofenadine HCI 30 mg

Purpose

Antihistamine

Uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, water eyes
  • itching of the nose or throat

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients.

Ask a doctor before use if you have

kidney disease. Your doctor should determine if you need a different dose.

When using this product

  • do not take more than directed
  • do not take at the same time as aluminum or magnesium antacids
  • do not take with fruit juices (see Directions)

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 use.

Keep out of reach of children.

In case of overdose, get medical help or contact a Poison Control Center right away.

Directions
  • place 1 tablet on tongue; tablet disintegrates, with or without water
adults and children 12 years of age and overtake 2 tablets every 12 hours on an empty stomach; do not take more than 4 tablets in 24 hours
children 6 to under 12 years of agetake 1 tablet every 12 hours on an empty stomach; do not take more than 2 tablets in 24 hours
children under 6 years of agedo not use
adults 65 years of age and olderask a doctor
consumers with kidney diseaseask a doctor

Other information
  • each tablet contains: sodium 5 mg
  • phenylketonurics: contains phenylalanine 5.3 mg per tablet
  • safety sealed: do not use if carton is opened or if individual blister units are torn or opened
  • store between 20º and 25ºC (68º and 77ºF)
  • use tablet immediately after opening individual blister

Inactive ingredients

aspartame, citric acid anhydrous, crospovidone, flavors, magnesium stearate, mannitol, methacrylic acid copolymer, microcrystalline cellulose, povidone, sodium bicarbonate, sodium starch glycolate

Questions or comments?

call toll-free 1-800-633-1610 or www.allegra.com 

Dist. By: Chattem, Inc.(part of the sanofi-aventis Group),

Chattanooga, TN 37409-0219 ©2010             50094020

PRINCIPAL DISPLAY PANEL

NDC 41167-4232-1
NON-DROWSY

Children’s

Allegra
® 
Allergy

fexofenadine
HCl orally disintegrating
tablet 30
mg/antihistamine
Indoor and Outdoor Allergies

Orange Cream flavored

12 Orally Disintegrating Tablets

CHILDRENS ALLEGRA ALLERGY 
fexofenadine hydrochloride tablet, orally disintegrating
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41167-4232
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE) FEXOFENADINE HYDROCHLORIDE30 mg
Inactive Ingredients
Ingredient NameStrength
ASPARTAME 
CROSPOVIDONE 
MAGNESIUM STEARATE 
LACTOSE MONOHYDRATE 
CELLULOSE, MICROCRYSTALLINE 
POVIDONE 
SILICON DIOXIDE 
Product Characteristics
ColorWHITEScoreno score
ShapeROUNDSize11mm
FlavorORANGE (Orange Cream) Imprint Codee;311;AV
Contains    
Packaging
#Item CodePackage Description
1NDC:41167-4232-12 BLISTER PACK in 1 CARTON
16 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
2NDC:41167-4232-64 BLISTER PACK in 1 CARTON
26 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
NDANDA02190901/02/2014
Labeler - Chattem, Inc. (003336013)

 
Chattem, Inc.

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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