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Childrens Allergy Fexofenadine Hydrochloride

Medically reviewed on December 21, 2017

Dosage form: suspension
Ingredients: FEXOFENADINE HYDROCHLORIDE 30mg in 5mL
Labeler: Meijer Distribution Inc
NDC Code: 41250-725

Childrens Allergy Fexofenadine Hydrochloride Oral Suspension

Drug Facts

ACTIVE INGREDIENT

(in each 5 mL = 1 teaspoonful)

Fexofenadine HCl, USP 30 mg

PURPOSE

Antihistamine

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

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
  • shake well before using
  • use only with enclosed dosing cup
     adults and children 12 years of age and over     take 2 teaspoonfuls (10 mL) every 12 hours; do not take more than 4 teaspoonfuls (20 mL) in 24 hours
     children 2 to under 12 years of age     take 1 teaspoonful (5 mL) every 12 hours; do not take more than 2 teaspoonfuls (10 mL) in 24 hours
     children under 2 years of age     ask a doctor
     adults 65 years of age and older     ask a doctor
     consumers with kidney disease     ask a doctor

OTHER INFORMATION
  • each 5 mL (1 teaspoonful) contains: sodium 18 mg
  • safety sealed: do not use if carton, unprinted foil inner seal, or neckband printed with “SEALED FOR YOUR PROTECTION” is opened, torn or missing.
  • store between 20º to 25ºC (68º to 77ºF)
  • before using any medication, read all label directions. Keep carton, it contains important information.

INACTIVE INGREDIENTS

artificial raspberry flavor, butylparaben, edetate disodium, poloxamer 407, propylene glycol, propylparaben, purified water, sodium phosphate dibasic, sodium phosphate monobasic, sucrose, titanium dioxide, xanthan gum, xylitol

QUESTIONS?

1-800-432-8534 between 9 am and 4 pm EST, Monday – Friday.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 41250-725-94

Compare to Children’s Allegra® Allergy active ingredient* 

meijer
Non-Drowsy
Ages 2 years and older

Children’s Allergy
Fexofenadine Hydrochloride Oral Suspension
30 mg/ 5mL
Antihistamine 

Berry Flavor
Dye Free 

12 Hour
Indoor and Outdoor Allergies 

Relief of:
Runny Nose/Sneezing
Itchy, Watery Eyes
Itchy Nose or Throat 

Alcohol Free

Use only with enclosed dosing cup. Wash and let air dry after each use.

4 FL OZ (118 mL)

CHILDRENS ALLERGY FEXOFENADINE HYDROCHLORIDE 
fexofenadine hydrochloride suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:41250-725
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FEXOFENADINE HYDROCHLORIDE (FEXOFENADINE) FEXOFENADINE HYDROCHLORIDE30 mg  in 5 mL
Inactive Ingredients
Ingredient NameStrength
BUTYLPARABEN 
EDETATE DISODIUM 
POLOXAMER 407 
PROPYLENE GLYCOL 
PROPYLPARABEN 
WATER 
SODIUM PHOSPHATE, DIBASIC, ANHYDROUS 
SODIUM PHOSPHATE, MONOBASIC, ANHYDROUS 
SUCROSE 
TITANIUM DIOXIDE 
XANTHAN GUM 
XYLITOL 
Product Characteristics
Color    Score    
ShapeSize
FlavorBERRYImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:41250-725-941 BOTTLE in 1 CARTON
1118 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20333012/19/2014
Labeler - Meijer Distribution Inc (006959555)
Registrant - Teva Pharmaceuticals USA, Inc. (001627975)

 
Meijer Distribution 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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